ARYL SULTAM DERIVATIVES AS RORc MODULATORS

CROSS REFERENCE TO RELATED APPLICATIONS

This application claims the benefit of priority of U.S. Provisional Patent Application Ser. No. 61/670,519 filed Jul. 11, 2012, U.S. Provisional Patent Application Ser. No. 61/788,430 filed Mar. 15, 2013 and U.S. Provisional Patent Application Ser. No. 61/837,461 filed Jun. 20, 2013, the disclosures of which are incorporated herein by reference in their entirety.

FIELD OF THE INVENTION

The invention pertains to compounds that modulate the function of retinoid-receptor related orphan receptor RORc (RORγ) and use of such compounds for treatment of autoimmune diseases

BACKGROUND OF THE INVENTION

T helper 17 cells (Th17) are interleukin (IL)-17 secreting CD4+ T cells involved in pathogenesis of autoimmune diseases such as rheumatoid arthritis, irritable bowel disease, psoriasis, psoriatic arthritis and spondyloarthridities. The retinoic acid-related orphan receptor γ (RORγ or RORc) is recognized as a transcription factor necessary for Th17 cell differentiation. RORc is an orphan member of the nuclear hormone receptor subfamily that includes RORα (RORa) and RORβ (RORb). RORc controls gene transcription by binding to DNA as a monomer. Selective modulation of RORc has been proposed as a route to discovery and development of Th17 cell-associated autoimmune diseases.

There is accordingly a need for compounds that inhibit RORc for use in treatment of autoimmune diseases such as rheumatoid arthritis, irritable bowel disease, psoriasis, psoriatic arthritis and spondyloarthridities.

SUMMARY OF THE INVENTION

The invention provides compounds of the formula I:

or a pharmaceutically acceptable salt thereof,

wherein:

m is 0 or 1;

n is 0 or 1;

p is from 0 to 3;

q is 0, 1 or 2;

r is from 1 to 3;

A is: a bond; —(CR_jR_k)_t—; —C(O)—(CR_jR_k)_t—; —(CR_jR_k)_t—C(O)—; —NR^a—(CR_jR_k)_t—; —(CR_jR_k)_t—NR^a—; —C(O)NR^a—(CR_jR_k)_t—; —(CR_jR_k)_t—NR^aC(O)—; —O—(CR_jR_k)_t—; —(CR_jR_k)_t—O—; —S—(CR_jR_k)_t—; —(CR_jR_k)_t—S—; —SO₂—(CR_jR_k)_t—; or —(CR_jR_k)_t—SO₂—;

t is from 0 to 4;

W is: —CR^bR^c—; —O—; —S—; —SO₂—; or —NR^d—;

one of X¹, X², X³ and X⁴ is N and the others are CR^e; or two of X¹, X², X³ and X⁴ are N and the others are CR^e; or three of X¹, X², X³ and X⁴ are N and the other is CR^e; or each of X¹, X², X³ and X⁴ is CR^e;

Y is: —O—; —S—; SO₂—; —CR^fR^g—; or —NR^h—;

Z is: CH; or N;

R¹, R², R³, R⁴, R⁵, R⁶, R⁷ and R⁸ each independently is: hydrogen; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo;

or R³ and R⁴ together with the atom to which they are attached may form an ethylene group;

or R³ and R⁴ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a- or —S—, and which may be optionally substituted one or more times with Rⁱ;

or R⁵ and R⁶ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or R⁷ and R⁸ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R³ and R⁴ together with one of R⁵ and R⁶ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R⁵ and R⁶ together with one of R⁷ and R⁸ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a- or —S—, and which may be optionally substituted one or more times with Rⁱ;

each R⁹ is independently: C_1-6alkyl; halo; C_1-6alkoxy; or cyano; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo;

R¹⁰ is: hydrogen; carboxy; C_1-6alkyl-carbonyl; C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; cyano; hydroxy-C₁₆alkyl; N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl; N-hydroxy-C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; halo; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo;

R¹¹ is: hydrogen; halo; carboxy; C_1-6alkyl-carbonyl; C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; C_1-6alkyl-sulfonylamino; C_1-6alkyl-sulfonylamino-C_1-6alkyl; cyano; hydroxy-C₁₆alkyl; N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl; N-hydroxy-C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo;

R¹² is: hydrogen; halo; carboxy; C_1-6alkyl-carbonyl; C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; cyano; hydroxy-C₁₆alkyl; N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl; N-hydroxy-C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo;

or R¹⁰ and R¹¹ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a- or —S—, and which may be optionally substituted one or more times with Rⁱ;

R^a, R^b, R^c and R^d each independent is: hydrogen; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo;

or R^b and R^c together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a- or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R^b and R^c together with one of R⁷ and R⁸ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R^b and R^c together with one of R⁵ and R⁶ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

each R^e is independently: hydrogen; C_1-6alkyl; halo; C_1-6alkoxy; or cyano; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo;

R^f is: hydrogen; halo; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo;

R^g is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkenyl; C_3-6cycloalkyl-C_1-6alkyl; halo; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; cyano-C_1-6alkyl-carbonyl; hydroxy-C_1-6alkyl-carbonyl; C_1-6alkoxy-C_1-6alkyl-carbonyl; carboxy; N-cyano-aminocarbonyl; N-cyano-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkyl-acetimidamidyl; N,N′-di-C_1-6alkyl-acetimidamidyl; N′-cyano-N—C_1-6alkyl-acetimidamidyl; N′-hydroxy-acetimidamidyl; N′—C_1-6alkoxy-acetimidamidyl; N′-hydroxy-N—C_1-6alkyl-acetimidamidyl; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl; 2-nitro-1-N—C_1-6alkylamino-vinyl; formyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; C_1-6alkyl-sulfonyl-C_1-6alkyl; aminocarbonyl; N-hydroxy-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; aminocarbonyl-C_1-6alkyl; N—C_1-6alkyl-aminocarbonyl-C_1-6alkyl; N,N-di-C_1-6alkyl-aminocarbonyl-C_1-6alkyl; C_1-6alkoxy-carbonyl; N-hydroxy-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkoxy; C_1-6alkyl-sulfonylamino; N—C_1-6alkyl-sulfonylaminocarbonyl; N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-amino-C_1-6alkyl; amino; N—C_1-6alkyl-amino; N,N-di-C_1-6alkyl-amino; halo-C_1-6alkyl; heterocyclyl; heteroaryl; or hydroxyl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the heterocyclyl, heteroaryl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ;

or R^f and R^g together with the atoms to which they are attached may form a four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

R^h is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkenyl; C_3-6cycloalkyl-C_1-6alkyl; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; cyano-C_1-6alkyl-carbonyl; hydroxy-C_1-6alkyl-carbonyl; C_1-6alkoxy-C_1-6alkyl-carbonyl; N-cyano-aminocarbonyl; N-cyano-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkyl-acetimidamidyl; N,N′-di-C_1-6alkyl-acetimidamidyl; N′-cyano-N—C_1-6alkyl-acetimidamidyl; N′-hydroxy-acetimidamidyl; N′—C_1-6alkoxy-acetimidamidyl; N′-hydroxy-N—C_1-6alkyl-acetimidamidyl; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl; 2-nitro-1-N—C_1-6alkylamino-vinyl; formyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; C_1-6alkyl-sulfonyl-C_1-6alkyl; aminocarbonyl; N-hydroxy-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N-hydroxy-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkyl-sulfonylamino; C_1-6alkyl-sulfonylamino-C_1-6alkyl; N—(C_1-6alkyl-sulfonyl)aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-amino-C_1-6alkyl; aminocarbonyl-C_1-6alkyl; N—C_1-6alkyl-aminocarbonyl-C_1-6alkyl; N,N-di-C_1-6alkyl-aminocarbonyl-C_1-6alkyl; C_1-6alkoxy-carbonyl; halo-C_1-6alkyl; heterocyclyl; or heteroaryl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the heterocyclyl, heteroaryl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ;

or R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached may form a four, five, six or seven membered aromatic, partially saturated or unsaturated ring that may optionally include one or two additional heteroatom selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ—;

or one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached may form a three, four, five, six or seven membered aromatic, partially saturated or unsaturated ring that may optionally include an additional heteroatom selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

Rⁱ is: C_1-6alkyl; halo; oxo; hydroxy; acetyl; C_1-6alkyl-carbonyl; amino-carbonyl; hydroxy-C_1-6alkyl; cyano; heteroaryl; or C_1-6alkoxy; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and

R^j and R^k each independent is: hydrogen; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo.

The invention also provides and pharmaceutical compositions comprising the compounds, methods of using the compounds, and methods of preparing the compounds.

DETAILED DESCRIPTION OF THE INVENTION

Definitions

Unless otherwise stated, the following terms used in this Application, including the specification and claims, have the definitions given below. It must be noted that, as used in the specification and the appended claims, the singular forms “a”, “an,” and “the” include plural referents unless the context clearly dictates otherwise.

“Alkyl” means the monovalent linear or branched saturated hydrocarbon moiety, consisting solely of carbon and hydrogen atoms, having from one to twelve carbon atoms. “Lower alkyl” refers to an alkyl group of one to six carbon atoms, i.e. C₁-C₆alkyl. Examples of alkyl groups include, but are not limited to, methyl, ethyl, propyl, isopropyl, isobutyl, sec-butyl, tert-butyl, pentyl, n-hexyl, octyl, dodecyl, and the like.

“Alkenyl” means a linear monovalent hydrocarbon radical of two to six carbon atoms or a branched monovalent hydrocarbon radical of three to six carbon atoms, containing at least one double bond, e.g., ethenyl, propenyl, and the like.

“Alkynyl” means a linear monovalent hydrocarbon radical of two to six carbon atoms or a branched monovalent hydrocarbon radical of three to six carbon atoms, containing at least one triple bond, e.g., ethynyl, propynyl, and the like.

“Alkylene” means a linear saturated divalent hydrocarbon radical of one to six carbon atoms or a branched saturated divalent hydrocarbon radical of three to six carbon atoms, e.g., methylene, ethylene, 2,2-dimethylethylene, propylene, 2-methylpropylene, butylene, pentylene, and the like.

“Alkoxy” and “alkyloxy”, which may be used interchangeably, mean a moiety of the formula —OR, wherein R is an alkyl moiety as defined herein. Examples of alkoxy moieties include, but are not limited to, methoxy, ethoxy, isopropoxy, and the like.

“Alkoxyalkyl” means a moiety of the formula R^a—O—R^b—, where R^a is alkyl and R^b is alkylene as defined herein. Exemplary alkoxyalkyl groups include, by way of example, 2-methoxyethyl, 3-methoxypropyl, 1-methyl-2-methoxyethyl, 1-(2-methoxyethyl)-3-methoxypropyl, and 1-(2-methoxyethyl)-3-methoxypropyl.

“Alkoxyalkoxy” means a group of the formula —O—R—R′ wherein R is alkylene and R′ is alkoxy as defined herein.

“Alkylcarbonyl” means a moiety of the formula —C(O)—R, wherein R is alkyl as defined herein.

“Alkoxycarbonyl” means a group of the formula —C(O)—R wherein R is alkoxy as defined herein.

“Alkylcarbonylalkyl” means a group of the formula —R—C(O)—R wherein R is alkylene and R′ is alkyl as defined herein.

“Alkoxyalkylcarbonyl” means a moiety of the formula —C(O)—R—R′, wherein R is alkylene and R′ is alkoxy as defined herein.

“Alkoxycarbonylalkyl” means a group of the formula —R—C(O)—R wherein R is alkylene and R′ is alkoxy as defined herein.

“Alkoxycarbonylalkoxy” means a group of the formula —O—R—C(O)—R′ wherein R is alkylene and R′ is alkoxy as defined herein.

“Hydroxycarbonylalkoxy” means a group of the formula —O—R—C(O)—OH wherein R is alkylene as defined herein.

“Alkylaminocarbonylalkoxy” means a group of the formula —O—R—C(O)—NHR′ wherein R is alkylene and R′ is alkyl as defined herein.

“Dialkylaminocarbonylalkoxy” means a group of the formula —O—R—C(O)—NR′R″ wherein R is alkylene and R′ and R″ are alkyl as defined herein.

“Alkylaminoalkoxy” means a group of the formula —O—R—NHR′ wherein R is alkylene and R′ is alkyl as defined herein.

“Dialkylaminoalkoxy” means a group of the formula —O—R—NR′R′ wherein R is alkylene and R′ and R″ are alkyl as defined herein.

“Alkylsulfonyl” means a moiety of the formula —SO₂—R, wherein R is alkyl as defined herein.

“Alkylsulfonylalkyl means a moiety of the formula —R′—SO₂—R” where R′ is alkylene and R″ is alkyl as defined herein.

“Alkylsulfonylalkoxy” means a group of the formula —O—R—SO₂—R′ wherein R is alkylene and R′ is alkyl as defined herein.

“Amino means a moiety of the formula —NRR′ wherein R and R′ each independently is hydrogen or alkyl as defined herein. “Amino thus includes “alkylamino (where one of R and R′ is alkyl and the other is hydrogen) and “dialkylamino (where R and R′ are both alkyl.

“Aminocarbonyl” means a group of the formula —C(O)—R wherein R is amino as defined herein.

“N-hydroxy-aminocarbonyl” means a group of the formula —C(O)—NR—OH wherein R is hydrogen or alkyl as defined herein.

“N-alkoxy-aminocarbonyl” means a group of the formula —C(O)—NR—R′ wherein R is hydrogen or alkyl and R′ is alkoxy as defined herein.

“N-alkyl-aminocarbonyl means a group of the formula —C(O)—NH—R wherein R is alkyl as defined herein.

“N-hydroxy-N-alkylaminocarbonyl means a group of the formula —C(O)—NRR′ wherein R is alkyl as defined herein and R′ is hydroxy.

“N-alkoxy-N-alkylaminocarbonyl” means a group of the formula —C(O)—NRR′ wherein R is alkyl and R′ is alkoxy as defined herein.

“N,N-di-C_1-6alkyl-aminocarbonyl” means a group of the formula —C(O)—NRR′ wherein R and R′ are alkyl as defined herein.

“Aminosulfonyl” means a group of the formula —SO₂—NH₂.

“N-alkylaminosulfonyl” means a group of the formula —SO₂—NHR wherein R is alkyl as defined herein.

“N,N-dialkylaminosulfonyl” means a group of the formula —SO₂—NRR′ wherein R and R′ are alkyl as defined herein.

“Alkylsulfonylamino” means a group of the formula —NR′—SO₂—R wherein R id alkyl and R′ is hydrogen or alkyl as defined herein.

“N-(alkylsulfonyl)-aminoalkyl” means a group of the formula —R—NH—SO₂—R′ wherein R is alkylene and R′ is alkyl as defined herein.

“N-(Alkylsulfonyl)aminocarbonyl” means a group of the formula —C(O)—NH—SO₂—R wherein wherein R is alkyl as defined herein.

“N-(Alkylsulfonyl)-N-alkylaminocarbonyl” means a group of the formula —C(O)—NR—SO₂—R′ wherein R and R′ are alkyl as defined herein.

“N-Alkoxyalkyl-aminocarbonyl” means a group of the formula —C(O)—NR—R′—OR″ wherein R is hydrogen or alkyl, R′ is alkylene, and R″ is alkyl as defined herein.

“N-Hydroxyalkyl-aminocarbonyl” means a group of the formula —C(O)—NR—R′—OH″ wherein R is hydrogen or alkyl and R′ is alkylene as defined herein.

“Alkoxyamino” means a moiety of the formula —NR—OR′ wherein R is hydrogen or alkyl and R′ is alkyl as defined herein.

“Alkylsulfanyl” means a moiety of the formula —SR wherein R is alkyl as defined herein.

“Aminoalkyl” means a group —R—R′ wherein R′ is amino and R is alkylene as defined herein. “Aminoalkyl” includes aminomethyl, aminoethyl, 1-aminopropyl, 2-aminopropyl, and the like. The amino moiety of “aminoalkyl” may be substituted once or twice with alkyl to provide “alkylaminoalkyl” and “dialkylaminoalkyl” respectively. “Alkylaminoalkyl” includes methylaminomethyl, methylaminoethyl, methylaminopropyl, ethylaminoethyl and the like.

“Dialkylaminoalkyl” includes dimethylaminomethyl, dimethylaminoethyl, dimethylaminopropyl, N-methyl-N-ethylaminoethyl, and the like.

“Aminoalkoxy” means a group —OR—R′ wherein R′ is amino and R is alkylene as defined herein.

“Alkylsulfonylamido” means a moiety of the formula —NR′SO₂—R wherein R is alkyl and R′ is hydrogen or alkyl.

“Aminocarbonyloxyalkyl” or “carbamylalkyl” means a group of the formula —R—O—C(O)—NR′R″ wherein R is alkylene and R′, R″ each independently is hydrogen or alkyl as defined herein.

“Alkynylalkoxy” means a group of the formula —O—R—R′ wherein R is alkylene and R′ is alkynyl as defined herein.

“N-Alkylacetimidamidyl” means a group of the formula

wherein R is alkyl as defined herein.

“N,N′-Dialkylacetimidamidyl” means a group of the formula

wherein R and R′ are both alkyl as defined herein.

“N′-Alkoxyacetimidamidyl” means a group of the formula

wherein R is alkoxy as defined herein.

“N′-Alkoxy-N-alkyl-acetimidamidyl” means a group of the formula

wherein R is alkyl and R′ is alkoxy as defined herein.

“Aryl” means a monovalent cyclic aromatic hydrocarbon moiety consisting of a mono-, bi- or tricyclic aromatic ring. The aryl group can be optionally substituted as defined herein. Examples of aryl moieties include, but are not limited to, phenyl, naphthyl, phenanthryl, fluorenyl, indenyl, pentalenyl, azulenyl, oxydiphenyl, biphenyl, methylenediphenyl, aminodiphenyl, diphenylsulfidyl, diphenylsulfonyl, diphenylisopropylidenyl, benzodioxanyl, benzofuranyl, benzodioxylyl, benzopyranyl, benzoxazinyl, benzoxazinonyl, benzopiperadinyl, benzopiperazinyl, benzopyrrolidinyl, benzomorpholinyl, methylenedioxyphenyl, ethylenedioxyphenyl, and the like, of which may be optionally substituted as defined herein.

“Arylalkyl” and “Aralkyl”, which may be used interchangeably, mean a radical-R^aR^b where R^a is an alkylene group and R^b is an aryl group as defined herein; e.g., phenylalkyls such as benzyl, phenylethyl, 3-(3-chlorophenyl)-2-methylpentyl, and the like are examples of arylalkyl.

“Arylsulfonyl means a group of the formula —SO₂—R wherein R is aryl as defined herein.

“Aryloxy” means a group of the formula —O—R wherein R is aryl as defined herein.

“Aralkyloxy” means a group of the formula —O—R—R″ wherein R is alkylene and R′ is aryl as defined herein.

“Carboxy” or “hydroxycarbonyl”, which may be used interchangeably, means a group of the formula —C(O)—OH.

“Cyanoalkyl” “means a moiety of the formula —R′—R”, where R′ is alkylene as defined herein and R″ is cyano or nitrile.

“Cycloalkyl” means a monovalent saturated carbocyclic moiety consisting of mono- or bicyclic rings. Particular cycloalkyl are unsubstituted or substituted with alkyl. Cycloalkyl can optionally be substituted as defined herein. Unless defined otherwise, cycloalkyl may be optionally substituted with one or more substituents, wherein each substituent is independently hydroxy, alkyl, alkoxy, halo, haloalkyl, amino, monoalkylamino, or dialkylamino Examples of cycloalkyl moieties include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and the like, including partially unsaturated (cycloalkenyl) derivatives thereof

“Cycloalkenyl” means a cycloalkyl as defined herein that includes at least one double bond or unsaturation. Exemplary cycloalkenyl include cyclohexenyl, cyclopentenyl, cyclobutenyl and the like.

“Cycloalkylalkyl” means a moiety of the formula —R′—R″, where R′ is alkylene and R″ is cycloalkyl as defined herein.

“Cycloalkylalkoxy” means a group of the formula —O—R—R′ wherein R is alkylene and R′ is cycloalkyl as defined herein.

“Cycloalkylcarbonyl” means a moiety of the formula —C(O)—R, wherein R is cycloalkyl as defined herein.

“C_3-6cycloalkyl-C_1-6alkyl-carbonyl” means a moiety of the formula —C(O)—R, wherein R is cycloalkylalkyl as defined herein.

“Cyanoalkylcarbonyl” means a moiety of the formula —C(O)—R—R′, wherein R is alkylene as defined herein and R′ is cyano or nitrile.

“N-Cyano-aminocarbonyl” means a moiety of the formula —C(O)—NHR, wherein R is cyano or nitrile.

“N-Cyano-N-alkyl-aminocarbonyl” means a moiety of the formula —C(O)—NRR′—R, wherein R′ is alkyl as defined herein and R is cyano or nitrile.

“Cycloalkylsulfonyl” means a group of the formula —SO₂—R wherein R is cycloalkyl as defined herein.

“Cycloalkylalkylsulfonyl” means a group of the formula —SO₂—R wherein R is cycloalkylalkyl as defined herein.

“N′-Cyanoacetimidamidyl” means a group of the formula

wherein R is cyano or nitrile.

“N′-Cyano-N-alkylacetimidamidyl” means a group of the formula

wherein R is alkyl as defined herein and R′ is cyano or nitrile.

“Formyl” means a moiety of the formula —C(O)—H.

“Heteroaryl” means a monocyclic or bicyclic radical of 5 to 12 ring atoms having at least one aromatic ring containing one, two, or three ring heteroatoms selected from N, O, or S, the remaining ring atoms being C, with the understanding that the attachment point of the heteroaryl radical will be on an aromatic ring. The heteroaryl ring may be optionally substituted as defined herein. Examples of heteroaryl moieties include, but are not limited to, optionally substituted imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, oxadiazolyl, thiadiazolyl, pyrazinyl, thienyl, benzothienyl, thiophenyl, furanyl, pyranyl, pyridyl, pyrrolyl, pyrazolyl, pyrimidyl, quinolinyl, isoquinolinyl, benzofuryl, benzothiophenyl, benzothiopyranyl, benzimidazolyl, benzooxazolyl, benzooxadiazolyl, benzothiazolyl, benzothiadiazolyl, benzopyranyl, indolyl, isoindolyl, triazolyl, triazinyl, quinoxalinyl, purinyl, quinazolinyl, quinolizinyl, naphthyridinyl, pteridinyl, carbazolyl, azepinyl, diazepinyl, acridinyl and the like, each of which may be optionally substituted as defined herein.

Heteroarylalkyl” or “heteroaralkyl” means a group of the formula —R—R′ wherein R is alkylene and R′ is heteroaryl as defined herein.

“Heteroarylsulfonyl means a group of the formula —SO₂—R wherein R is heteroaryl as defined herein.

“Heteroaryloxy” means a group of the formula —O—R wherein R is heteroaryl as defined herein.

“Heteroaralkyloxy” means a group of the formula —O—R—R″ wherein R is alkylene and R′ is heteroaryl as defined herein.

The terms “halo”, “halogen” and “halide”, which may be used interchangeably, refer to a substituent fluoro, chloro, bromo, or iodo.

“Haloalkyl” means alkyl as defined herein in which one or more hydrogen has been replaced with same or different halogen. Exemplary haloalkyls include —CH₂Cl, —CH₂CF₃, —CH₂CCl₃, perfluoroalkyl (e.g., —CF₃), and the like.

“Haloalkoxy” means a moiety of the formula —OR, wherein R is a haloalkyl moiety as defined herein. An exemplary haloalkoxy is difluoromethoxy.

“Heterocycloamino” means a saturated ring wherein at least one ring atom is N, NH or N-alkyl and the remaining ring atoms form an alkylene group.

“Heterocyclyl” means a monovalent saturated moiety, consisting of one to three rings, incorporating one, two, or three or four heteroatoms (chosen from nitrogen, oxygen or sulfur). The heterocyclyl ring may be optionally substituted as defined herein. Examples of heterocyclyl moieties include, but are not limited to, optionally substituted piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, azepinyl, pyrrolidinyl, azetidinyl, tetrahydropyranyl, tetrahydrofuranyl, oxetanyl and the like. Such heterocyclyl may be optionally substituted as defined herein.

“Heterocyclylalkyl” means a moiety of the formula —R—R′ wherein R is alkylene and R′ is heterocyclyl as defined herein.

“Heterocyclyloxy” means a moiety of the formula —OR wherein R is heterocyclyl as defined herein.

“Heterocyclylalkoxy” means a moiety of the formula —OR—R′ wherein R is alkylene and R′ is heterocyclyl as defined herein.

“Hydroxyalkoxy” means a moiety of the formula —OR wherein R is hydroxyalkyl as defined herein.

“Hydroxyalkylamino” means a moiety of the formula —NR—R′ wherein R is hydrogen or alkyl and R′ is hydroxyalkyl as defined herein.

“Hydroxyalkylaminoalkyl” means a moiety of the formula —R—NR′—R″ wherein R is alkylene, R′ is hydrogen or alkyl, and R″ is hydroxyalkyl as defined herein.

“Hydroxycarbonylalkyl” or “carboxyalkyl” means a group of the formula —R—(CO)—OH where R is alkylene as defined herein.

“Hydroxycarbonylalkoxy” means a group of the formula —O—R—C(O)—OH wherein R is alkylene as defined herein.

“Hydroxyalkylcarbonyl” means a moiety of the formula —C(O)—R—R′, wherein R is alkylene as defined herein and R′ is hydroxy.

“N′ hydroxyacetimidamidyl” means a group of the formula

“N′-hydroxy-N-alkyl-acetimidamidyl” means a group of the formula

wherein R is alkyl as defined herein.

“Hydroxyalkyloxycarbonylalkyl” or “hydroxyalkoxycarbonylalkyl” means a group of the formula —R—C(O)—O—R—OH wherein each R is alkylene and may be the same or different.

“Hydroxyalkyl” means an alkyl moiety as defined herein, substituted with one or more, for example, one, two or three hydroxy groups, provided that the same carbon atom does not carry more than one hydroxy group. Representative examples include, but are not limited to, hydroxymethyl, 2-hydroxyethyl, 2-hydroxypropyl, 3-hydroxypropyl, 1-(hydroxymethyl)-2-methylpropyl, 2-hydroxybutyl, 3-hydroxybutyl, 4-hydroxybutyl, 2,3-dihydroxypropyl, 2-hydroxy-1-hydroxymethylethyl, 2,3-dihydroxybutyl, 3,4-dihydroxybutyl and 2-(hydroxymethyl)-3-hydroxypropyl

“Hydroxycycloalkyl” means a cycloalkyl moiety as defined herein wherein one, two or three hydrogen atoms in the cycloalkyl radical have been replaced with a hydroxy substituent. Representative examples include, but are not limited to, 2-, 3-, or 4-hydroxycyclohexyl, and the like.

“2-Nitro-1-N-alkylamino-vinyl” means a group of the formula

wherein R is alkyl as defined herein.

“Oxo” means a group of the formula ═O (i.e., an oxygen with a double bond). Thus, for example, a 1-oxo-ethyl group is an acetyl group.

“Alkoxy hydroxyalkyl” and “hydroxy alkoxyalkyl”, which may be used interchangeably, means an alkyl as defined herein that is substituted at least once with hydroxy and at least once with alkoxy. “Alkoxy hydroxyalkyl” and “hydroxy alkoxyalkyl” thus encompass, for example, 2-hydroxy-3-methoxy-propan-1-yl and the like.

“Urea” or “ureido” means a group of the formula —NR′—C(O)—NR″R′″ wherein R′, R″ and R′″ each independently is hydrogen or alkyl.

“Carbamate” means a group of the formula —O—C(O)—NR′R″ wherein R′ and R″ each independently is hydrogen or alkyl.

“Carboxy” means a group of the formula —O—C(O)—OH.

“Sulfonamido” means a group of the formula —SO₂—NR′R″ wherein R′, R″ and R′″ each independently is hydrogen or alkyl.

“Optionally substituted” when used in association with an “aryl”, phenyl”, “heteroaryl” “cycloalkyl” or “heterocyclyl” moiety means that such moiety may be unsubstituted (i.e., all open valencies are occupied by a hydrogen atom) or substituted with specific groups as related herein.

“Leaving group” means the group with the meaning conventionally associated with it in synthetic organic chemistry, i.e., an atom or group displaceable under substitution reaction conditions. Examples of leaving groups include, but are not limited to, halogen, alkane- or arylenesulfonyloxy, such as methanesulfonyloxy, ethanesulfonyloxy, thiomethyl, benzenesulfonyloxy, tosyloxy, and thienyloxy, dihalophosphinoyloxy, optionally substituted benzyloxy, isopropyloxy, acyloxy, and the like.

“Modulator” means a molecule that interacts with a target. The interactions include, but are not limited to, agonist, antagonist, and the like, as defined herein.

“Optional” or “optionally” means that the subsequently described event or circumstance may but need not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not.

“Disease” and “Disease state” means any disease, condition, symptom, disorder or indication.

“Inert organic solvent” or “inert solvent” means the solvent is inert under the conditions of the reaction being described in conjunction therewith, including for example, benzene, toluene, acetonitrile, tetrahydrofuran, N,N-dimethylformamide, chloroform, methylene chloride or dichloromethane, dichloroethane, diethyl ether, ethyl acetate, acetone, methyl ethyl ketone, methanol, ethanol, propanol, isopropanol, tert-butanol, dioxane, pyridine, and the like. Unless specified to the contrary, the solvents used in the reactions of the present invention are inert solvents.

“Pharmaceutically acceptable” means that which is useful in preparing a pharmaceutical composition that is generally safe, non-toxic, and neither biologically nor otherwise undesirable and includes that which is acceptable for veterinary as well as human pharmaceutical use.

“Pharmaceutically acceptable salts” of a compound means salts that are pharmaceutically acceptable, as defined herein, and that possess the desired pharmacological activity of the parent compound.

It should be understood that all references to pharmaceutically acceptable salts include solvent addition forms (solvates) or crystal forms (polymorphs) as defined herein, of the same acid addition salt.

“Protective group” or “protecting group” means the group which selectively blocks one reactive site in a multifunctional compound such that a chemical reaction can be carried out selectively at another unprotected reactive site in the meaning conventionally associated with it in synthetic chemistry. Certain processes of this invention rely upon the protective groups to block reactive nitrogen and/or oxygen atoms present in the reactants. For example, the terms “amino-protecting group” and “nitrogen protecting group” are used interchangeably herein and refer to those organic groups intended to protect the nitrogen atom against undesirable reactions during synthetic procedures. Exemplary nitrogen protecting groups include, but are not limited to, trifluoroacetyl, acetamido, benzyl (Bn), benzyloxycarbonyl (carbobenzyloxy, CBZ), p-methoxybenzyloxycarbonyl, p-nitrobenzyloxycarbonyl, tert-butoxycarbonyl (BOC), and the like. The artisan in the art will know how to chose a group for the ease of removal and for the ability to withstand the following reactions.

“Solvates” means solvent additions forms that contain either stoichiometric or non stoichiometric amounts of solvent. Some compounds have a tendency to trap a fixed molar ratio of solvent molecules in the crystalline solid state, thus forming a solvate. If the solvent is water the solvate formed is a hydrate, when the solvent is alcohol, the solvate formed is an alcoholate. Hydrates are formed by the combination of one or more molecules of water with one of the substances in which the water retains its molecular state as H₂O, such combination being able to form one or more hydrate.

“Arthritis” means a disease or condition that causes damage to joints of the body and pain associated with such joint damage. Arthritis includes rheumatoid arthritis, osteoarthritis, psoriatic arthritis, septic arthritis, spondyloarthropathies, gouty arthritis, systemic lupus erythematosus and juvenile arthritis, osteoarthritis, and other arthritic conditions.

“Respiratory disorder” refers to, without limitation, chronic obstructive pulmonary disease (COPD), asthma, bronchospasm, and the like.

“Gastrointestinal disorder” (“GI disorder”) refers to, without limitation, Irritable Bowel Syndrome (IBS), Inflammatory Bowel Disease (IBD), biliary colic and other biliary disorders, renal colic, diarrhea-dominant IBS, pain associated with GI distension, and the like.

“Pain” includes, without limitation, inflammatory pain; surgical pain; visceral pain; dental pain; premenstrual pain; central pain; pain due to burns; migraine or cluster headaches; nerve injury; neuritis; neuralgias; poisoning; ischemic injury; interstitial cystitis; cancer pain; viral, parasitic or bacterial infection; post-traumatic injury; or pain associated with irritable bowel syndrome.

“Subject” means mammals and non-mammals. Mammals means any member of the mammalia class including, but not limited to, humans; non-human primates such as chimpanzees and other apes and monkey species; farm animals such as cattle, horses, sheep, goats, and swine; domestic animals such as rabbits, dogs, and cats; laboratory animals including rodents, such as rats, mice, and guinea pigs; and the like. Examples of non-mammals include, but are not limited to, birds, and the like. The term “subject” does not denote a particular age or sex.

“Therapeutically effective amount” means an amount of a compound that, when administered to a subject for treating a disease state, is sufficient to effect such treatment for the disease state. The “therapeutically effective amount” will vary depending on the compound, disease state being treated, the severity or the disease treated, the age and relative health of the subject, the route and form of administration, the judgment of the attending medical or veterinary practitioner, and other factors.

The terms “those defined above” and “those defined herein” when referring to a variable incorporates by reference the broad definition of the variable as well as particular definitions, if any.

“Treating” or “treatment” of a disease state includes, inter alia, inhibiting the disease state, i.e., arresting the development of the disease state or its clinical symptoms, and/or relieving the disease state, i.e., causing temporary or permanent regression of the disease state or its clinical symptoms.

The terms “treating”, “contacting” and “reacting” when referring to a chemical reaction means adding or mixing two or more reagents under appropriate conditions to produce the indicated and/or the desired product. It should be appreciated that the reaction which produces the indicated and/or the desired product may not necessarily result directly from the combination of two reagents which were initially added, i.e., there may be one or more intermediates which are produced in the mixture which ultimately leads to the formation of the indicated and/or the desired product.

Nomenclature and Structures

In general, the nomenclature and chemical names used in this Application are based on ChembioOffice™ by CambridgeSoft™. Any open valency appearing on a carbon, oxygen sulfur or nitrogen atom in the structures herein indicates the presence of a hydrogen atom unless indicated otherwise. Where a nitrogen-containing heteroaryl ring is shown with an open valency on a nitrogen atom, and variables such as R^a, R^b or R^c are shown on the heteroaryl ring, such variables may be bound or joined to the open valency nitrogen. Where a chiral center exists in a structure but no specific stereochemistry is shown for the chiral center, both enantiomers associated with the chiral center are encompassed by the structure. Where a structure shown herein may exist in multiple tautomeric forms, all such tautomers are encompassed by the structure. The atoms represented in the structures herein are intended to encompass all naturally occurring isotopes of such atoms. Thus, for example, the hydrogen atoms represented herein are meant to include deuterium and tritium, and the carbon atoms are meant to include C¹³ and C¹⁴ isotopes. One or more carbon atom(s) of a compound of the invention may be replaced by a silicon atom(s), and it is contemplated that one or more oxygen atom(s) of a compound of the invention may be replaced by a sulfur or selenium atom(s).

Compounds of the Invention

The invention provides compounds of the formula I:

or a pharmaceutically acceptable salt thereof,

wherein:

m is 0 or 1;

n is 0 or 1;

p is from 0 to 3;

q is 0, 1 or 2;

r is from 1 to 3;

A is: a bond; —(CR_jR_k)_t—; —C(O)—(CR_jR_k)_t—; —(CR_jR_k)_t—C(O)—; —NR^a—(CR_jR_k)_t—; —(CR_jR_k)_t—NR^a—; —C(O)NR^a—(CR_jR_k)_t—; —(CR_jR_k)_t—NR^aC(O)—; —O—(CR_jR_k)_t—; —(CR_jR_k)_t—O—; —S—(CR_jR_k)_t—; —(CR_jR_k)_t—S—; —SO₂—(CR_jR_k)_t—; or —(CR_jR_k)_t—SO₂—;

t is from 0 to 4;

W is: —CR^bR^c—; —O—; —S—; —SO₂—; or —NR^d—;

one of X¹, X², X³ and X⁴ is N and the others are CR^e; or two of X¹, X², X³ and X⁴ are N and the others are CR^e; or three of X¹, X², X³ and X⁴ are N and the other is CR^e; or each of X¹, X², X³ and X⁴ is CR^e;

Y is: —O—; —S—; SO₂—; —CR^fR^g—; or —NR^h—;

Z is: CH; or N;

R¹, R², R³, R⁴, R⁵, R⁶, R⁷ and R⁸ each independently is: hydrogen; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo;

or R³ and R⁴ together with the atom to which they are attached may form an ethylene group;

or R³ and R⁴ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or R⁵ and R⁶ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or R⁷ and R⁸ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R³ and R⁴ together with one of R⁵ and R⁶ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R⁵ and R⁶ together with one of R⁷ and R⁸ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

each R⁹ is independently: C_1-6alkyl; halo; C_1-6alkoxy; or cyano; wherein the C_1-6 alkyl moieties may be unsubstituted or substituted one or more times with halo;

R¹⁰ is: hydrogen; carboxy; C_1-6alkyl-carbonyl; C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; cyano; hydroxy-C₁₆alkyl; N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl; N-hydroxy-C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; halo; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo;

R¹¹ is: hydrogen; halo; carboxy; C_1-6alkyl-carbonyl; C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; C_1-6alkyl-sulfonylamino; C_1-6alkyl-sulfonylamino-C_1-6alkyl; cyano; hydroxy-C₁₆alkyl; N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl; N-hydroxy-C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo;

R¹² is: hydrogen; halo; carboxy; C_1-6alkyl-carbonyl; C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; cyano; hydroxy-C₁₆alkyl; N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl; N-hydroxy-C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo;

or R¹⁰ and R¹¹ together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

R^a, R^b, R^c and R^d each independent is: hydrogen; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo;

or R^b and R^c together with the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R^b and R^c together with one of R⁷ and R⁸ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

or one of R^b and R^c together with one of R⁵ and R⁶ and the atoms to which they are attached may form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

each R^e is independently: hydrogen; C_1-6alkyl; halo; C_1-6alkoxy; or cyano; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo;

R^f is: hydrogen; halo; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo;

R^g is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkenyl; C_3-6cycloalkyl-C_1-6alkyl; halo; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; cyano-C_1-6alkyl-carbonyl; hydroxy-C_1-6alkyl-carbonyl; C_1-6alkoxy-C_1-6alkyl-carbonyl; carboxy; N-cyano-aminocarbonyl; N-cyano-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkyl-acetimidamidyl; N,N′-di-C_1-6alkyl-acetimidamidyl; N′-cyano-N—C_1-6alkyl-acetimidamidyl; N′-hydroxy-acetimidamidyl; N′—C_1-6alkoxy-acetimidamidyl; N′-hydroxy-N—C_1-6alkyl-acetimidamidyl; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl; 2-nitro-1-N—C_1-6alkylamino-vinyl; formyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; C_1-6alkyl-sulfonyl-C_1-6alkyl; aminocarbonyl; N-hydroxy-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; aminocarbonyl-C_1-6alkyl; N—C_1-6alkyl-aminocarbonyl-C_1-6alkyl; N,N-di-C_1-6alkyl-aminocarbonyl-C_1-6alkyl; C_1-6alkoxy-carbonyl; N-hydroxy-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkoxy; C_1-6alkyl-sulfonylamino; N—C_1-6alkyl-sulfonylaminocarbonyl; N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-amino-C_1-6alkyl; amino; N—C_1-6alkyl-amino; N,N-di-C_1-6alkyl-amino; halo-C_1-6alkyl; heterocyclyl; heteroaryl; or hydroxyl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the heterocyclyl, heteroaryl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ;

or R^f and R^g together with the atoms to which they are attached may form a four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

R^h is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkenyl; C_3-6cycloalkyl-C_1-6alkyl; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; cyano-C_1-6alkyl-carbonyl; hydroxy-C_1-6alkyl-carbonyl; C_1-6alkoxy-C_1-6alkyl-carbonyl; N-cyano-aminocarbonyl; N-cyano-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkyl-acetimidamidyl; N,N′-di-C_1-6alkyl-acetimidamidyl; N′-cyano-N—C_1-6alkyl-acetimidamidyl; N′-hydroxy-acetimidamidyl; N′—C_1-6alkoxy-acetimidamidyl; N′-hydroxy-N—C_1-6alkyl-acetimidamidyl; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl; 2-nitro-1-N—C_1-6alkylamino-vinyl; formyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; C_1-6alkyl-sulfonyl-C_1-6alkyl; aminocarbonyl; N-hydroxy-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N-hydroxy-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkyl-sulfonylamino; C_1-6alkyl-sulfonylamino-C_1-6alkyl; N—(C_1-6alkyl-sulfonyl)aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-amino-C_1-6alkyl; aminocarbonyl-C_1-6alkyl; N—C_1-6alkyl-aminocarbonyl-C_1-6alkyl; N,N-di-C_1-6alkyl-aminocarbonyl-C_1-6alkyl; C_1-6alkoxy-carbonyl; halo-C_1-6alkyl; heterocyclyl; or heteroaryl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the heterocyclyl, heteroaryl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ;

or R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached may form a four, five, six or seven membered aromatic, partially saturated or unsaturated ring that may optionally include one or two additional heteroatom selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ—;

or one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached may form a three, four, five, six or seven membered aromatic, partially saturated or unsaturated ring that may optionally include an additional heteroatom selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ;

Rⁱ is: C_1-6alkyl; halo; oxo; hydroxy; acetyl; C_1-6alkyl-carbonyl; amino-carbonyl; hydroxy-C_1-6alkyl; cyano; heteroaryl; or C_1-6alkoxy; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and

R^j and R^k each independent is: hydrogen; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo.

In certain embodiments of formula I, when A is a heteroatom, then X is —CH—.

In certain embodiments of formula I, when Y is a heteroatom, then q is 1 or 2.

In certain embodiments of formula I, when Y and Z are heteroatom, then q is 2 and r is 2 or 3.

In certain embodiments of formula I, when Z is a heteroatom and A is —(CR_jR_k)_t—; —NR^a—(CR_jR_k)_t; —O—(CR_jR_k)_t; —S—(CR_jR_k)_t; or —SO₂—(CR_jR_k)_t; then t is from 2 to 4.

In certain embodiments of formula I, m is 0.

In certain embodiments of formula I, m is 1.

In certain embodiments of formula I, n is 0.

In certain embodiments of formula I, n is 1.

In certain embodiments of formula I, p is from 0 to 2.

In certain embodiments of formula I, p is 0 or 1.

In certain embodiments of formula I, p is 0.

In certain embodiments of formula I, p is 1.

In certain embodiments of formula I, p is 2.

In certain embodiments of formula I, p is 3.

In certain embodiments of formula I, q is 0.

In certain embodiments of formula I, q is 1.

In certain embodiments of formula I, q is 2.

In certain embodiments of formula I, r is 1.

In certain embodiments of formula I, r is 2.

In certain embodiments of formula I, r is 3.

In certain embodiments of formula I, t is from 0 to 3.

In certain embodiments of formula I, t is 0.

In certain embodiments of formula I, t is 1.

In certain embodiments of formula I, t is 2.

In certain embodiments of formula I, t is 3.

In certain embodiments of formula I, A is: a bond; —CH₂—; —C(O)—; —NR^a—; —O—; —S—; or —SO₂—.

In certain embodiments of formula I, A is: a bond; —(CR_jR_k)_t—; —C(O)—(CR_jR_k)_t—; —(CR_jR_k)_t—C(O)—; —(CR_jR_k)_t—NR^a—; —C(O)NR^a—(CR_jR_k)_t—; —(CR_jR_k)_t—NR^aC(O)—; —(CR_jR_k)_t—O—; —(CR_jR_k)_t—S—; or —(CR_jR_k)_t—SO₂—.

In certain embodiments of formula I, A is: a bond; —C(O)—(CR_jR_k)_t—; —(CR_jR_k)_t—C(O)—; —(CR_jR_k)_t—NR^a—; —C(O)NR^a—(CR_jR_k)_t—; (CR_jR_k)_t—NR^aC(O)—; or —(CR_jR_k)_t—O—.

In certain embodiments of formula I, A is: a bond; —NR^a—; —O—; or —S—.

In certain embodiments of formula I, A is: a bond; —NR^a—; or —O—.

In certain embodiments of formula I, A is a bond.

In certain embodiments of formula I, A is —CH₂—.

In certain embodiments of formula I, A is —C(O)—.

In certain embodiments of formula I, A is

In certain embodiments of formula I, A is —O—.

In certain embodiments of formula I, A is —S—.

In certain embodiments of formula I, A is —SO₂—.

In certain embodiments of formula I, A is —C(O)NR^a—(CH₂)_t.

In certain embodiments of formula I, A is —(CH₂)_t—NR^aC(O)—.

In certain embodiments of formula I, A is —(CR_jR_k)_t—.

In certain embodiments of formula I, A is —CR_jR_k—.

In certain embodiments of formula I, A is —C(O)—(CR_jR_k)_t—.

In certain embodiments of formula I, A is —(CR_jR_k)_t—C(O)—.

In certain embodiments of formula I, A is —NR^a—(CR_jR_k)_t—.

In certain embodiments of formula I, A is —(CR_jR_k)_t—NR^a—.

In certain embodiments of formula I, A is —C(O)NR^a—(CR_jR_k)_t—.

In certain embodiments of formula I, A is (CR_jR_k)_t—NR^aC(O)—.

In certain embodiments of formula I, A is —O—(CR_jR_k)_t—.

In certain embodiments of formula I, A is —(CR_jR_k)_t—O—.

In certain embodiments of formula I, A is —S—(CR_jR_k)_t—.

In certain embodiments of formula I, A is —(CR_jR_k)_t—S—.

In certain embodiments of formula I, A is —SO₂—(CR_jR_k)_t—.

In certain embodiments of formula I, A is —(CR_jR_k)_t—SO₂—.

In certain embodiments of formula I, A is —(CH₂)₂—O—.

In certain embodiments of formula I, A is —(CH₂)—O—.

In certain embodiments of formula I, A is —O—(CH₂)₂—.

In certain embodiments of formula I, A is —O—(CH₂)—.

In certain embodiments of formula I, A is —(CH₂)₂—C(O)—.

In certain embodiments of formula I, A is —(CH₂)—C(O)—.

In certain embodiments of formula I, A is —C(O)—(CH₂)₂—.

In certain embodiments of formula I, A is —C(O)—(CH₂)—.

In certain embodiments of formula I, A is —C(O)—NH—.

In certain embodiments of formula I, A is —CH₂—C(O)—NH—.

In certain embodiments of formula I, A is —NH—.

In certain embodiments of formula I, A is —(CH₂)₂—NH—.

In certain embodiments of formula I, A is —CH₂—NH—.

In certain embodiments of formula I, A is —NH—(CH₂)₂—.

In certain embodiments of formula I, A is —NH—CH₂—.

In certain embodiments of formula I, A is —NH—C(O)—.

In certain embodiments of formula I, t is from 0 to 3.

In certain embodiments of formula I, t is from 1 to 3.

In certain embodiments of formula I, t is from 0 to 2.

In certain embodiments of formula I, t is 0.

In certain embodiments of formula I, t is 1.

In certain embodiments of formula I, t is 2.

In certain embodiments of formula I, t is 3.

In certain embodiments of formula I, t is 4.

In certain embodiments of formula I, W is —CR^bR^c— or —O—.

In certain embodiments of formula I, W is —CR^bR^c—.

In certain embodiments of formula I, W is —O—.

In certain embodiments of formula I, W is —NR^d—.

In certain embodiments of formula I, W is —S—.

In certain embodiments of formula I, W is —SO₂—.

In certain embodiments of formula I, W is —CH₂—.

In certain embodiments of formula I, one or two of X¹, X², X³ and X⁴ is N and the others are CR^e.

In certain embodiments of formula I, three of X¹, X², X³ and X⁴ are CR^e and the other is N.

In certain embodiments of formula I, X¹, X², X³ and X⁴ are CR^e.

In certain embodiments of formula I, X¹ is N and X², X³ and X⁴ are CR^e.

In certain embodiments of formula I, X² is N and X¹, X³ and X⁴ are CR^e.

In certain embodiments of formula I, X¹ and X⁴ are N, and X² and X³ are CR^a.

In certain embodiments of formula I, X² and X³ are N, and X¹ and X⁴ are CR^e.

In certain embodiments of formula I, X¹ and X² are N, and X³ and X⁴ are CR^e.

In certain embodiments of formula I, Y is —O—, —CR^fR^g— or —NR^h—.

In certain embodiments of formula I, Y is —CR^fR^g— or —NR^h—.

In certain embodiments of formula I, Y is —O—.

In certain embodiments of formula I, Y is —S—.

In certain embodiments of formula I, Y is —SO₂—.

In certain embodiments of formula I, Y is —CR^fR^g—.

In certain embodiments of formula I, Y is —NR^h—.

In certain embodiments of formula I, Z is CH.

In certain embodiments of formula I, Z is N.

In certain embodiments of formula I, each R¹ is independently: C_1-6alkyl; halo; C_1-6alkoxy; cyano; halo-C_1-6alkyl; or halo-C_1-6alkoxy.

In certain embodiments of formula I, R¹ is hydrogen.

In certain embodiments of formula I, R¹ is C_1-6alkyl.

In certain embodiments of formula I, R² is hydrogen.

In certain embodiments of formula I, R² is C_1-6alkyl.

In certain embodiments of formula I, R³ is hydrogen.

In certain embodiments of formula I, R³ is C_1-6alkyl.

In certain embodiments of formula I, R⁴ is hydrogen.

In certain embodiments of formula I, R⁴ is C_1-6alkyl.

In certain embodiments of formula I, R⁵ is hydrogen.

In certain embodiments of formula I, R⁵ is C_1-6alkyl.

In certain embodiments of formula I, R⁶ is hydrogen.

In certain embodiments of formula I, R⁶ is C_1-6alkyl.

In certain embodiments of formula I, R⁷ is hydrogen.

In certain embodiments of formula I, R⁷ is C_1-6alkyl.

In certain embodiments of formula I, R⁸ is hydrogen.

In certain embodiments of formula I, R⁸ is C_1-6alkyl.

In certain embodiments of formula I, R³ and R⁴ together with the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, R³ and R⁴ together with the atoms to which they are attached form a three, four or five membered saturated ring.

In certain embodiments of formula I, R⁵ and R⁶ together with the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, R⁵ and R⁶ together with the atoms to which they are attached form a three, four or five membered saturated ring.

In certain embodiments of formula I, R⁷ and R⁸ together with the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, R⁷ and R⁸ together with the atoms to which they are attached form a three, four or five membered saturated ring.

In certain embodiments of formula I, one of R³ and R⁴ together with one of R⁵ and R⁶ and the atoms to which they are attached form a three, four, five, six or seven membered ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, one of R⁵ and R⁶ together with one of R⁷ and R⁸ and the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, each R⁹ is independently: C_1-6alkyl; halo; or halo-C_1-6alkyl.

In certain embodiments of formula I, R⁹ is C_1-6alkyl.

In certain embodiments of formula I, R⁹ is halo.

In certain embodiments of formula I, R⁹ is C_1-6alkoxy.

In certain embodiments of formula I, R⁹ is cyano.

In certain embodiments of formula I, R⁹ is halo-C_1-6alkyl.

In certain embodiments of formula I, each R⁹ is independently: fluoro; chloro; or trifluoromethyl.

In certain embodiments of formula I, R¹⁰ is: hydrogen; halo; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo.

In certain embodiments of formula I, R¹⁰ is: hydrogen or C_1-6alkyl.

In certain embodiments of formula I, R¹⁰ is hydrogen.

In certain embodiments of formula I, R¹⁰ is C_1-6alkyl.

In certain embodiments of formula I, R¹⁰ is methyl.

In certain embodiments of formula I, R¹⁰ is halo.

In certain embodiments of formula I, R¹⁰ is carboxy.

In certain embodiments of formula I, R¹⁰ is C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R¹⁰ is C_1-6alkoxy-carbonyl. In certain embodiments of formula I, R¹⁰ is oxo.

In certain embodiments of formula I, R¹⁰ is hydroxy.

In certain embodiments of formula I, R¹⁰ is aminocarbonyl.

In certain embodiments of formula I, R¹⁰ is N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹⁰ is N,N-di-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹⁰ is cyano

In certain embodiments of formula I, R¹⁰ is hydroxy-C_1-6alkyl.

In certain embodiments of formula I, R¹⁰ is N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹⁰ is N-hydroxy-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹⁰ is N—C_1-6alkoxy-aminocarbonyl.

In certain embodiments of formula I, R¹¹ is: hydrogen; halo; oxo; hydroxy; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo; or oxo.

In certain embodiments of formula I, R¹¹ is: hydrogen; halo; carboxy; C_1-6alkyl-carbonyl;

C_1-6alkoxy-carbonyl; oxo; hydroxy; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; or C_1-6alkyl which may be unsubstituted or substituted one or more times with halo or oxo.

In certain embodiments of formula I, R¹¹ is: hydrogen; halo; or C_1-6alkyl.

In certain embodiments of formula I, R¹¹ is: hydrogen; C_1-6alkyl; or halo.

In certain embodiments of formula I, R¹¹ is: hydrogen; or C_1-6alkyl.

In certain embodiments of formula I, R¹¹ is hydrogen.

In certain embodiments of formula I, R¹¹ is C_1-6alkyl

In certain embodiments of formula I, R¹⁰¹ is methyl.

In certain embodiments of formula I, R¹¹ is halo.

In certain embodiments of formula I, R¹¹ is oxo.

In certain embodiments of formula I, R¹¹ is C_1-6alkyl-sulfonylamino

In certain embodiments of formula I, R¹¹ is C_1-6alkyl-sulfonylamino-C_1-6alkyl.

In certain embodiments of formula I, R¹¹ is cyano.

In certain embodiments of formula I, R¹¹ is hydroxy-C_1-6alkyl.

In certain embodiments of formula I, R¹¹ is N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹¹ is N-hydroxy-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹¹ is N—C_1-6alkoxy-aminocarbonyl.

In certain embodiments of formula I, R¹² is: hydrogen; or C_1-6alkyl.

In certain embodiments of formula I, R¹² is hydrogen.

In certain embodiments of formula I, R¹² is halo.

In certain embodiments of formula I, R¹² is carboxy.

In certain embodiments of formula I, R¹² is C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R¹² is C_1-6alkoxy-carbonyl.

In certain embodiments of formula I, R¹² is oxo.

In certain embodiments of formula I, R¹² is hydroxy.

In certain embodiments of formula I, R¹² is aminocarbonyl.

In certain embodiments of formula I, R¹² is N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹² is N,N-di-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹² is cyano.

In certain embodiments of formula I, R¹² is hydroxy-C_1-6alkyl.

In certain embodiments of formula I, R¹² is N—C_1-6alkoxy-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹² is N-hydroxy-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R¹² is N—C_1-6alkoxy-aminocarbonyl.

In certain embodiments of formula I, R¹² is C_1-6alkyl.

In certain embodiments of formula I, R¹² is methyl.

In certain embodiments of formula I, R¹⁰ and R¹¹ together with the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, R¹⁰ and R¹¹ together with the atoms to which they are attached form a four, five, six or seven membered ring;

In certain embodiments of formula I, R^a is hydrogen.

In certain embodiments of formula I, R^a is C_1-6alkyl.

In certain embodiments of formula I, R^b is hydrogen.

In certain embodiments of formula I, R^b is C_1-6alkyl.

In certain embodiments of formula I, R^c is hydrogen.

In certain embodiments of formula I, R^c is C_1-6alkyl.

In certain embodiments of formula I, R^b and R^c together with the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, one of R^b and R^c together with one of R⁷ and R⁸ and the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, one of R^b and R^c together with one of R⁵ and R⁶ and the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring that may optionally include one or two heteroatoms selected from —O—, —NR^a— or —S—, and which may be optionally substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^d is hydrogen.

In certain embodiments of formula I, R^d is C_1-6alkyl.

In certain embodiments of formula I, each R^e is independently: hydrogen; C_1-6alkyl; halo; or halo-C_1-6alkyl.

In certain embodiments of formula I, each R^e is independently: hydrogen; C_1-6alkyl; or halo.

In certain embodiments of formula I, each R^e is independently: hydrogen; or halo.

In certain embodiments of formula I, each R^e is independently: hydrogen; or fluoro.

In certain embodiments of formula I, R^e is hydrogen.

In certain embodiments of formula I, R^e is C_1-6alkyl.

In certain embodiments of formula I, R^e is halo.

In certain embodiments of formula I, R^e is C_1-6alkoxy.

In certain embodiments of formula I, R^e is cyano. In certain embodiments of formula I, R^e is halo-C_1-6alkyl.

In certain embodiments of formula I, each R^f is independently: hydrogen; or C_1-6alkyl.

In certain embodiments of formula I, R^f is hydrogen.

In certain embodiments of formula I, R^f is C_1-6alkyl.

In certain embodiments of formula I, R^f is halo.

In certain embodiments of formula I, R^g is: C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkenyl; C_3-6cycloalkyl-C_1-6alkyl; halo; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; cyano-C_1-6alkyl-carbonyl; hydroxy-C_1-6alkyl-carbonyl; C_1-6alkoxy-C_1-6alkyl-carbonyl; carboxy; N-cyano-aminocarbonyl; N-cyano-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkyl-acetimidamidyl; N,N′-di-C_1-6alkyl-acetimidamidyl; N′-cyano-N—C_1-6alkyl-acetimidamidyl; N′-hydroxy-acetimidamidyl; N′—C_1-6alkoxy-acetimidamidyl; N′-hydroxy-N—C_1-6alkyl-acetimidamidyl; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl; 2-nitro-1-N—C_1-6alkylamino-vinyl; formyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; C_1-6alkyl-sulfonyl-C_1-6alkyl; aminocarbonyl; N-hydroxy-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N-hydroxy-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkoxy; C_1-6alkyl-sulfonylamino; N—C_1-6alkyl-sulfonylaminocarbonyl; N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-amino-C_1-6alkyl; amino; N—C_1-6alkyl-amino; N,N-di-C_1-6alkyl-amino; halo-C_1-6alkyl; heterocyclyl; heteroaryl; or hydroxyl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the heterocyclyl, heteroaryl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkyl-C_1-6alkyl; halo; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkoxy; C_1-6alkyl-sulfonylamino; amino; N—C_1-6alkyl-amino; N,N-di-C_1-6alkyl-amino; halo-C_1-6alkyl; or hydroxyl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the C_3-6cycloalkyl, and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is hydrogen.

In certain embodiments of formula I, R^g is C_1-6alkyl.

In certain embodiments of formula I, R^g is C_3-6cycloalkyl which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is C_3-6cycloalkyl-C_1-6alkyl which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is halo.

In certain embodiments of formula I, R^g is C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^g is C_3-6cycloalkyl-carbonyl wherein the C_3-6cycloalkyl moeity may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is C_3-6cycloalkyl-C_1-6alkyl-carbonyl wherein the C_3-6cycloalkyl-C_1-6alkyl moiety may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is C_1-6alkyl-sulfonyl.

In certain embodiments of formula I, R^g is C_3-6cycloalkyl-sulfonyl.

In certain embodiments of formula I, R^g is C_3-6cycloalkyl-C_1-6alkyl-sulfonyl.

In certain embodiments of formula I, R^g is aminocarbonyl.

In certain embodiments of formula I, R^g is N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^g is N,N-di-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^g is aminosulfonyl.

In certain embodiments of formula I, R^g is N—C_1-6alkyl-aminosulfonyl.

In certain embodiments of formula I, R^g is N,N-di-C_1-6alkyl-aminosulfonyl.

In certain embodiments of formula I, R^g is cyano.

In certain embodiments of formula I, R^g is C_1-6alkoxy.

In certain embodiments of formula I, R^g is C_1-6alkyl-sulfonylamino

In certain embodiments of formula I, R^g is amino

In certain embodiments of formula I, R^g is N—C_1-6alkyl-amino

In certain embodiments of formula I, R^g is N,N-di-C_1-6alkyl-amino

In certain embodiments of formula I, R^g is halo-C_1-6alkyl.

In certain embodiments of formula I, R^g is hydroxy.

In certain embodiments of formula I, R^g is C_3-6cycloalkeny which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is cyano-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^g is hydroxy-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^g is C_1-6alkoxy-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^g is carboxy.

In certain embodiments of formula I, R^g is N-cyano-aminocarbonyl.

In certain embodiments of formula I, R^g is N-cyano-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^g is N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^g is N,N′-di-C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^g is N′-cyano-N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^g is N′-hydroxy-acetimidamidyl.

In certain embodiments of formula I, R^g is N′—C_1-6alkoxy-acetimidamidyl.

In certain embodiments of formula I, R^g is N′-hydroxy-N—C_1-6alkyl-acetimidamide; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^g is 2-nitro-1-N—C_1-6alkylamino-vinyl.

In certain embodiments of formula I, R^g is C_1-6alkyl-sulfonyl-C_1-6alkyl.

In certain embodiments of formula I, R^g is N-hydroxy-aminocarbonyl.

In certain embodiments of formula I, R^g is N—C_1-6alkoxy-aminocarbonyl.

In certain embodiments of formula I, R^g is N-hydroxy-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^g is N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^g is N—C_1-6alkyl-sulfonylaminocarbonyl.

In certain embodiments of formula I, R^g is N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^g is aminocarbonyl-C_1-6alkyl.

In certain embodiments of formula I, R^g is N—C_1-6alkyl-aminocarbonyl-C_1-6alkyl

In certain embodiments of formula I, R^g is N,N-di-C_1-6alkyl-aminocarbonyl-C_1-6alkyl.

In certain embodiments of formula I, R^g is C_1-6alkoxy-carbonyl.

In certain embodiments of formula I, R^g is heterocyclyl which may be unsubstituted or substituted one or more times with Rⁱ.

In embodiments of formula I wherein R^g is heterocyclyl, such heterocyclyl may be oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, azetidinyl, pyrrolidinyl, piperidinyl, azepinyl or piperazinyl, each of which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is heteroaryl which may be unsubstituted or substituted one or more times with Rⁱ.

In embodiments of formula I wherein R^g is heteroaryl, such heteroaryl may be pyridinyl, pyrimidinyl, triazinyl, pyrrolyl, imidazolyl, pyrazoyl, triazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, thiadiazolyl or tetrazolyl, each of which may be unsubstituted or substituted one or more times with Rⁱ.

In embodiments of formula I wherein R^g is heteroaryl, such heteroaryl may be imidazolyl, pyrazoyl, triazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, thiadiazolyl or tetrazolyl, each of which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^g is triazolyl.

In certain embodiments of formula I, R^g is [1,2,4]triazol-4-yl.

In certain embodiments of formula I, R^g is [1,2,4]triazol-3-yl.

In certain embodiments of formula I, R^g is 4-methyl-[1,2,4]triazol-3-yl.

In certain embodiments of formula I, R^g is [1,2,4]triazol-1-yl.

In certain embodiments of formula I, R^g is [1,2,3]triazol-1-yl.

In certain embodiments of formula I, R^g is [1,2,3]triazol-4-yl.

In certain embodiments of formula I, R^g is 4-methyl-[1,2,4]triazol-3-yl.

In certain embodiments of formula I, R^g is pyrazolyl.

In certain embodiments of formula I, R^g is pyrazol-3-yl.

In certain embodiments of formula I, R^g is pyrazol-1-yl.

In certain embodiments of formula I, R^g is pyrazol-4-yl.

In certain embodiments of formula I, R^g is imidazolyl.

In certain embodiments of formula I, R^g is imidazol-1-yl.

In certain embodiments of formula I, R^g is 1-methyl-imidazol-2-yl.

In certain embodiments of formula I, R^g is isoxazolyl.

In certain embodiments of formula I, R^g is 3-hydroxyisoxazol-5-yl.

In certain embodiments of formula I, R^g is oxdiazolyl.

In certain embodiments of formula I, R^g is [1,2,4]oxadiazol-5-yl.

In certain embodiments of formula I, R^g is [1,2,4]oxadiazol-3-yl.

In certain embodiments of formula I, R^g is [1,2,3]oxadiazol-2-yl.

In certain embodiments of formula I, R^g is [1,2,3]oxadiazol-2-one-5-yl.

In certain embodiments of formula I, R^g is tetrazolyl.

In certain embodiments of formula I, R^g is tetrazol-5-yl.

In certain embodiments of formula I, R^g is tetrazol-1-yl.

In certain embodiments of formula I, R^g is tetrazol-2-yl.

In certain embodiments of formula I, R^g is pyrazolyl.

In certain embodiments of formula I, R^g is pyridazinyl.

In certain embodiments of formula I, R^g is triazinyl.

In certain embodiments of formula I, R^f and R^g together with the atoms to which they are attached form a three, four, five, six or seven membered saturated or partially saturated ring.

In certain embodiments of formula I, R^f and R^g together with the atoms to which they are attached form a three membered ring.

In certain embodiments of formula I, R^f and R^g together with the atoms to which they are attached form a four membered ring.

In certain embodiments of formula I, R^f and R^g together with the atoms to which they are attached form a five membered ring.

In certain embodiments of formula I, R^f and R^g together with the atoms to which they are attached form a six membered ring.

In certain embodiments of formula I, R^f and R^g together with the atoms to which they are attached form a seven membered ring.

In certain embodiments of formula I, R^h is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkenyl; C_3-6cycloalkyl-C_1-6alkyl; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; cyano-C_1-6alkyl-carbonyl; hydroxy-C_1-6alkyl-carbonyl; C_1-6alkoxy-C_1-6alkyl-carbonyl; N-cyano-aminocarbonyl; N-cyano-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkyl-acetimidamidyl; N,N′-di-C_1-6alkyl-acetimidamidyl; N′-cyano-N—C_1-6alkyl-acetimidamidyl; N′-hydroxy-acetimidamidyl; N′—C_1-6alkoxy-acetimidamidyl; N′-hydroxy-N—C_1-6alkyl-acetimidamidyl; N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl; 2-nitro-1-N—C_1-6alkylamino-vinyl; formyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; C_1-6alkyl-sulfonyl-C_1-6alkyl; aminocarbonyl; N-hydroxy-aminocarbonyl; N—C_1-6alkoxy-aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N-hydroxy-N—C_1-6alkyl-aminocarbonyl; N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; N,N-di-C_1-6alkyl-aminosulfonyl; cyano; C_1-6alkyl-sulfonylamino; C_1-6alkyl-sulfonylamino-C_1-6alkyl; N—(C_1-6alkyl-sulfonyl)aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl; N—(C_1-6alkyl-sulfonyl)-amino-C_1-6alkyl; halo-C_1-6alkyl; heterocyclyl; or heteroaryl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the heterocyclyl, heteroaryl, C_3-6cycloalkyl, C_3-6cycloalkenyl and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is: hydrogen; C_1-6alkyl; C_3-6cycloalkyl; C_3-6cycloalkyl-C_1-6alkyl; C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; or N,N-di-C_1-6alkyl-aminosulfonyl; wherein the C_1-6alkyl moieties may be unsubstituted or substituted one or more times with halo; and wherein the C_3-6cycloalkyl, and C_3-6cycloalkyl-C_1-6alkyl moieties may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is: C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl;

C_3-6cycloalkyl-C_1-6alkyl-carbonyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; aminocarbonyl; N—C_1-6alkyl-aminocarbonyl; or N,N-di-C_1-6alkyl-aminocarbonyl; aminosulfonyl; N—C_1-6alkyl-aminosulfonyl; or N,N-di-C_1-6alkyl-aminosulfonyl; wherein the C_3-6cycloalkyl, and C_3-6cycloalkyl-C_1-6alkyl moieties each may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is: C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; C_3-6cycloalkyl-C_1-6alkyl-carbonyl; C_1-6alkyl-sulfonyl; C_3-6cycloalkyl-sulfonyl; or C_3-6cycloalkyl-C_1-6alkyl-sulfonyl; wherein the C_3-6cycloalkyl, and C_3-6cycloalkyl-C_1-6alkyl moieties each may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is: C_1-6alkyl-carbonyl; C_3-6cycloalkyl-carbonyl; or C_3-6cycloalkyl-C_1-6alkyl-carbonyl; wherein the C_3-6cycloalkyl, and C_3-6cycloalkyl-C_1-6alkyl moieties each may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is hydrogen.

In certain embodiments of formula I, R^h is C_1-6alkyl.

In certain embodiments of formula I, R^h is C_3-6cycloalkyl which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is C_3-6cycloalkyl-C_1-6alkyl.

In certain embodiments of formula I, R^h is C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^h is C_3-6cycloalkyl-carbonyl.

In certain embodiments of formula I, R^h is C_3-6cycloalkyl-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^h is C_1-6alkyl-sulfonyl.

In certain embodiments of formula I, R^h is C_3-6cycloalkyl-sulfonyl.

In certain embodiments of formula I, R^h is C_3-6cycloalkyl-C_1-6alkyl-sulfonyl.

In certain embodiments of formula I, R^h is aminocarbonyl.

In certain embodiments of formula I, R^h is N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^h is N,N-di-C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^h is aminosulfonyl.

In certain embodiments of formula I, R^h is N—C_1-6alkyl-aminosulfonyl.

In certain embodiments of formula I, R^h is or N,N-di-C_1-6alkyl-aminosulfonyl.

In certain embodiments of formula I, R^h is C_3-6cycloalkenyl.

In certain embodiments of formula I, R^h is cyano-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^h is hydroxy-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^h is C_1-6alkoxy-C_1-6alkyl-carbonyl.

In certain embodiments of formula I, R^h is N-cyano-aminocarbonyl.

In certain embodiments of formula I, R^h is N-cyano-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^h is N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^h is N,N′-di-C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^h is N′-cyano-N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^h is N′-hydroxy-acetimidamidyl.

In certain embodiments of formula I, R^h is N′—C_1-6alkoxy-acetimidamidyl.

In certain embodiments of formula I, R^h is N′-hydroxy-N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^h is N′—C_1-6alkoxy-N—C_1-6alkyl-acetimidamidyl.

In certain embodiments of formula I, R^h is 2-nitro-1-N—C_1-6alkylamino-vinyl.

In certain embodiments of formula I, R^h is C_1-6alkyl-sulfonyl-C_1-6alkyl.

In certain embodiments of formula I, R^h is N-hydroxy-aminocarbonyl.

In certain embodiments of formula I, R^h is N—C_1-6alkoxy-aminocarbonyl.

In certain embodiments of formula I, R^h is N-hydroxy-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^h is N—C_1-6alkoxy-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^h is C_1-6alkyl-sulfonylamino-C_1-6alkyl.

In certain embodiments of formula I, R^h is N—(C_1-6alkyl-sulfonyl)aminocarbonyl.

In certain embodiments of formula I, R^h is N—(C_1-6alkyl-sulfonyl)-N—C_1-6alkyl-aminocarbonyl.

In certain embodiments of formula I, R^h is aminocarbonyl-C_1-6alkyl.

In certain embodiments of formula I, R^h is N—C_1-6alkyl-aminocarbonyl-C_1-6alkyl

In certain embodiments of formula I, R^h is N,N-di-C_1-6alkyl-aminocarbonyl-C_1-6alkyl.

In certain embodiments of formula I, R^h is C_1-6alkoxy-carbonyl.

In certain embodiments of formula I, R^h is heterocyclyl which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is heteroaryl which may be unsubstituted or substituted one or more times with Rⁱ.

In embodiments of formula I wherein R^h is heteroaryl, such heteroaryl may be pyridinyl, pyrimidinyl, pyrolyl, imidazolyl, pyrazoyl, triazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, thiadiazolyl or tetrazolyl, each of which may be unsubstituted or substituted one or more times with Rⁱ.

In embodiments of formula I wherein R^h is heteroaryl, such heteroaryl may be imidazolyl, pyrazoyl, triazolyl, oxazolyl, thiazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, thiadiazolyl or tetrazolyl, each of which may be unsubstituted or substituted one or more times with Rⁱ.

In certain embodiments of formula I, R^h is acetyl.

In certain embodiments of formula I, R^h is methanesulfonyl.

In certain embodiments of formula I, R^h is cyclopropylcarbonyl.

In certain embodiments of formula I, R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a four, five, six or seven membered aromatic, partially saturated or unsaturated ring.

In certain embodiments of formula I, R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a four membered ring.

In certain embodiments of formula I, R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a five membered ring.

In certain embodiments of formula I, R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a six membered ring.

In certain embodiments of formula I, R^h and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a seven membered ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a four, five, six or seven membered aromatic, partially saturated or unsaturated ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a five or six membered aromatic ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a five membered aromatic ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a six membered aromatic ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a five or six membered saturated ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a five membered saturated ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a six membered saturated ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a four membered ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a five membered ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a six membered ring.

In certain embodiments of formula I, one of R^f and R^g and one of R¹⁰ and R¹¹ together with the atoms to which they are attached form a seven membered ring.

In certain embodiments of formula I, Rⁱ is: C_1-6alkyl; halo; oxo; hydroxy; acetyl; or C_1-6alkoxy.

In certain embodiments of formula I, Rⁱ is C_1-6alkyl.

In certain embodiments of formula I, Rⁱ is halo.

In certain embodiments of formula I, Rⁱ is C_1-6alkoxy.

In certain embodiments of formula I, Rⁱ is halo-C_1-6alkyl.

In certain embodiments of formula I, Rⁱ is oxo.

In certain embodiments of formula I, Rⁱ is hydroxy.

In certain embodiments of formula I, Rⁱ is acetyl.

In certain embodiments of formula I, Rⁱ is C_1-6alkyl-carbonyl.

In certain embodiments of formula I, Rⁱ is amino-carbonyl.

In certain embodiments of formula I, Rⁱ is hydroxy-C_1-6alkyl.

In certain embodiments of formula I, Rⁱ is cyano.

In certain embodiments of formula I, Rⁱ is heteroaryl;

In certain embodiments of formula I, R^j and R^k each independent is: hydrogen; or methyl.

In certain embodiments of formula I, R^j is hydrogen.

In certain embodiments of formula I, R^k is hydrogen.

In certain embodiments of the invention, the group

is:

In certain embodiments of formula I, the subject compounds may be of formula Ia or Ib:

wherein m, n, p, q, r, A, W, X¹, X², X³, X⁴, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰ and R¹¹, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula Ia.

In certain embodiments, the subject compounds are of formula Ib.

In certain embodiments of formula I, the subject compounds may be of formula IIa or IIb

wherein s is from 0 to 3,

and m, n, p, q, r, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula IIa.

In certain embodiments, the subject compounds are of formula IIb.

In certain embodiments of formula IIa or IIb, R^e is halo.

In certain embodiments of formula IIa or IIb, R^e is fluoro.

In certain embodiments of formula IIa or IIb, s is 0 or 1.

In certain embodiments of formula IIa or IIb, s is 0.

In certain embodiments of formula IIa or IIb, s is 1.

In certain embodiments of formula IIa or IIb, s is 1 or 2.

In certain embodiments of formula IIa or IIb, s is 2.

In certain embodiments of formula IIa or IIb, s is 1, 2 or 3.

In certain embodiments of formula IIa or IIb, s is 2 or 3.

In certain embodiments of formula IIa or IIb, s is 3.

In certain embodiments of formula I, the subject compounds may be of formula IIIa or IIb:

wherein m, n, p, q, r, s, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula IIIa.

In certain embodiments, the subject compounds are of formula IIIb.

In certain embodiments of formula I, the subject compounds may be of formula IVa or IVb

wherein m, n, p, q, r, s, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula IVa.

In certain embodiments, the subject compounds are of formula IVb.

In certain embodiments of formula I, the subject compounds may be of formula Va or Vb:

wherein m, n, p, q, r, s, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula Va.

In certain embodiments, the subject compounds are of formula Vb.

In certain embodiments of formula I, the subject compounds may be of formula VIa or VIb:

wherein m, n, p, q, r, s, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula VIa.

In certain embodiments, the subject compounds are of formula VIb.

In certain embodiments of formula I, the subject compounds may be of formula VIIa or VIIb:

wherein m, n, p, q, r, s, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula VIIa.

In certain embodiments, the subject compounds are of formula VIIb.

In certain embodiments of formula I, the subject compounds may be of formula VIIIa or VIIIb:

wherein m, n, p, q, r, s, A, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula VIIIa.

In certain embodiments, the subject compounds are of formula VIIIb.

In certain embodiments of formula I, the subject compounds may be of formula IXa or IXb:

wherein m, n, p, q, r, s, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula IXa.

In certain embodiments, the subject compounds are of formula IXb.

In certain embodiments of formula I, the subject compounds may be of formula Xa or Xb:

wherein m, n, p, q, r, s, W, Y, Z, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula Xa.

In certain embodiments, the subject compounds are of formula Xb.

In certain embodiments of formula I, the subject compounds may be of formula XIa or XIb:

wherein m, n, p, s, W, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XIa.

In certain embodiments, the subject compounds are of formula XIb.

In certain embodiments of formula I, the subject compounds may be of formula XIIa or XIIb:

wherein m, n, p, s, W, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XIIa.

In certain embodiments, the subject compounds are of formula XIIb.

In certain embodiments of formula I, the subject compounds may be of formula XIIIa or XIIIb;

wherein m, n, p, s, W, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^a, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XIIIa.

In certain embodiments, the subject compounds are of formula XIIIb.

In certain embodiments of formula I, the subject compounds may be of formula XIVa or XIVb:

wherein m, n, p, s, W, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XIVa.

In certain embodiments, the subject compounds are of formula XIVb.

In certain embodiments of formula I, the subject compounds may be of formula XVa or XVb:

wherein m, n, p, s, W, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XVa.

In certain embodiments, the subject compounds are of formula XVb.

In certain embodiments of formula I, the subject compounds may be of formula XVIa or XVIb:

wherein m, n, p, s, W, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R¹¹, R^e and R^g are as defined herein.

In certain embodiments, the subject compounds are of formula XVIa.

In certain embodiments, the subject compounds are of formula XVIb.

In certain embodiments of formula I, the subject compounds may be of formula XVIIa or XVIIb:

wherein p, q, r, s, A, Y, Z, R¹, R², R³, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula XVIIa.

In certain embodiments, the subject compounds are of formula XVIIb.

In certain embodiments of formula I, the subject compounds may be of formula XVIIIa or XVIIIb:

wherein p, q, r, s, Y, Z, R¹, R², R³, R⁹, R¹⁰, R¹¹ and R^e, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula XVIIIa.

In certain embodiments, the subject compounds are of formula XVIIIb.

In certain embodiments of formula I, the subject compounds may be of formula XIXa or XIXb:

wherein m, n, p, s, R¹, R², R³, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XIXa.

In certain embodiments, the subject compounds are of formula XIXb.

In certain embodiments of formula I, the subject compounds may be of formula XXa or XXb:

wherein m, n, p, s, R¹, R², R³, R⁹, R¹⁰, R¹¹, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XXa.

In certain embodiments, the subject compounds are of formula XXb.

In certain embodiments of formula I, the subject compounds may be of formula XXIa or XXIb;

wherein m, n, p, s, R¹, R², R³, R⁹, R¹⁰, R¹¹, R^a, R^e and R^h are as defined herein.

In certain embodiments, the subject compounds are of formula XXIa.

In certain embodiments, the subject compounds are of formula XXIb.

In certain embodiments of formula I, the subject compounds may be of formula XXIIa or XXIIb:

wherein m, n, p, s, R¹, R², R³, R⁹, R¹⁰, R¹¹, R^e and R^g are as defined herein.

In certain embodiments, the subject compounds are of formula XXIIa.

In certain embodiments, the subject compounds are of formula XXIIb.

In certain embodiments, the subject compounds may be of one of formulas XXIIIa through XIIId:

wherein R^m1, R^m2, R^m3 and R^m4 each independently is: hydrogen; or halo; and p, q, r, A, Y, Z, R³, R⁹, R¹⁰, and R¹¹, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula XXIIIa.

In certain embodiments, the subject compounds are of formula XXIIIb.

In certain embodiments, the subject compounds are of formula XXIIIc.

In certain embodiments, the subject compounds are of formula XXIIId.

In certain embodiments, R^m1, R^m2, R^m3 and R^m4 each independently is: hydrogen; or fluoro.

In certain embodiments, R^m1 is fluoro and R^m2, R^m3 and R^m4 are hydrogen.

In certain embodiments, R^m2 is fluoro and R^m1, R^m3 and R^m4 are hydrogen.

In certain embodiments, R^m3 is fluoro and R^m1, R^m2 and R^m4 are hydrogen.

In certain embodiments, R^m1 and R^m2 are fluoro and R^m3 and R^m4 are hydrogen.

In certain embodiments, R^m1 and R^m3 are fluoro and R^m2 and R^m4 are hydrogen.

In certain embodiments, R^m1 and R^m4 are fluoro and R^m2 and R^m3 are hydrogen.

In certain embodiments, R^m1, R^m2 and R^m4 are fluoro and R^m3 is hydrogen.

In certain embodiments, R^m1, R^m2, R^m3 and R^m4 are fluoro.

In certain embodiments, the subject compounds may be of one of formula XXIVa through XXIVd:

wherein p, q, r, Y, Z, R³, R⁹, R¹⁰, R¹¹, R^m1, R^m2, R^m3 and R^m4, and the group

are as defined herein.

In certain embodiments, the subject compounds are of formula XXIXa.

In certain embodiments, the subject compounds are of formula XXIXb.

In certain embodiments, the subject compounds are of formula XXIXc.

In certain embodiments, the subject compounds are of formula XXIXd.

In certain embodiments of formula I, the subject compounds may be of one of formulas XXVa through XXVd:

wherein p, R³, R⁹, R¹⁰, R¹¹, R^h, R^m1, R^m2, R^m3, and R^m4 are as defined herein.

In certain embodiments, the subject compounds are of formula XXVa.

In certain embodiments, the subject compounds are of formula XXVb.

In certain embodiments, the subject compounds are of formula XXVc.

In certain embodiments, the subject compounds are of formula XXVd.

In certain embodiments of formula I, the subject compounds may be of one of formulas XXVIa through XXVId:

wherein p, R³, R⁹, R¹⁰, R¹¹, R^h, R^m1, R^m2, R^m3 and R^m4 are as defined herein.

In certain embodiments, the subject compounds are of formula XXVIa.

In certain embodiments, the subject compounds are of formula XXVIb.

In certain embodiments, the subject compounds are of formula XXVIc.

In certain embodiments, the subject compounds are of formula XXVId.

In certain embodiments of formula I, the subject compounds may be of one of formulas XXVIIa through XXVIId;

wherein p, R³, R⁹, R¹⁰, R¹¹, R^h, R^m1, R^m2, R^m3 and R^m4 are as defined herein.

In certain embodiments, the subject compounds are of formula XXVIIa.

In certain embodiments, the subject compounds are of formula XXVIIb.

In certain embodiments, the subject compounds are of formula XXVIIc.

In certain embodiments, the subject compounds are of formula XXVIId.

In certain embodiments of formula I, the subject compounds may be of one of formulas XXVIIIa through XXVIIId:

wherein p, R³, R⁹, R¹⁰, R¹¹, R^h, R^m1, R^m2, R^m3 and R^m4 are as defined herein.

In certain embodiments, the subject compounds are of formula XXVIIIa.

In certain embodiments, the subject compounds are of formula XXVIIIb.

In certain embodiments, the subject compounds are of formula XXVIIIc.

In certain embodiments, the subject compounds are of formula XXVIIId.

Methods

The invention also provides a method for treating a disease or condition mediated by or otherwise associated with the RORc receptor, the method comprising administering to a subject in need thereof an effective amount of a compound of the invention.

The disease may be arthritis such as rheumatoid arthritis or osteoarthritis.

The disease may be asthma or COPD.

Representative compounds in accordance with the methods of the invention are shown in the experimental examples below.

Synthesis

Compounds of the present invention can be made by a variety of methods depicted in the illustrative synthetic reaction schemes shown and described below.

The starting materials and reagents used in preparing these compounds generally are either available from commercial suppliers, such as Aldrich Chemical Co., or are prepared by methods known to those skilled in the art following procedures set forth in references such as Fieser and Fieser's Reagents for Organic Synthesis; Wiley & Sons: New York, 1991, Volumes 1-15; Rodd's Chemistry of Carbon Compounds, Elsevier Science Publishers, 1989, Volumes 1-5 and Supplementals; and Organic Reactions, Wiley & Sons: New York, 1991, Volumes 1-40. The following synthetic reaction schemes are merely illustrative of some methods by which the compounds of the present invention can be synthesized, and various modifications to these synthetic reaction schemes can be made and will be suggested to one skilled in the art having referred to the disclosure contained in this Application.

The starting materials and the intermediates of the synthetic reaction schemes can be isolated and purified if desired using conventional techniques, including but not limited to, filtration, distillation, crystallization, chromatography, and the like. Such materials can be characterized using conventional means, including physical constants and spectral data.

Unless specified to the contrary, the reactions described herein may be conducted under an inert atmosphere at atmospheric pressure at a reaction temperature range of from about −78° C. to about 150° C., for example, from about 0° C. to about 125° C., or conveniently at about room (or ambient) temperature, e.g., about 20° C.

Scheme A below illustrates one synthetic procedure usable to prepare specific compounds of formula I, wherein LG is a leaving group such as halo, sulfonate, or the like, and m, n, p, q, A, X¹, X², X³, X⁴, R¹, R², R³, R⁴, R⁵, R⁶, R⁷, R⁸, R⁹, R¹⁰, R^b and R^c are as defined herein.

In step 1 of Scheme A, alkyl amine a is reacted with benzyl sulfonyl chloride b to form sulfonamide compound c. The reaction of step 1 may be carried out in a polar aprotic solvent such as THF or methylene chloride, and in the presence of a tertiary amine base or weak base such as potassium carbonate. The leaving group of compound a may be bromo in certain embodiments. Similarly, the chloro group of compound b may in certain embodiments be replaced by other halo or leaving group.

A cyclization reaction is carried out in step 2 to afford thiazinane compound d. The cyclization may be achieved in the presence of a strong base such as an alkyl lithium reagent, using polar aprotic solvent under anhydrous conditions.

In step 3, thiazinane compound c is reacted with aryalkyl halide compound e to yield aralkyl thiazinane f. The reaction of step 3 may be carried out in the presence of a strong base such as sodium hydride under anhydrous polar aprotic solvent conditions. The bromo groups of compound e may be replaced by other suitable leaving groups used in the art.

Thiazinane compound f may be treated with reagent g in step 4A to provide sultam compound h, which is a compound of formula I in accordance with the invention. In embodiments wherein A is oxygen such that reagent g is a cyclic alcohol, the reaction of step 4A may utilize a copper catalyst with hydrophobic solvent, in the presence of cesium carbonate or like base.

Alternatively, step 4B may be carried out wherein Thiazinane compound f undergoes amination by reaction with cyclic amine i to afford sultam compound j, which is a compound of formula I in accordance with the invention. The reaction of step may utilize a suitable palladium catalyst under Buchwald reaction conditions.

Scheme B below shows another synthetic procedure usable to prepare specific compounds of formula I, wherein TBS is tri-(tert-butyl)-silyl, and m, n, p, q, A, X¹, X², X³, X⁴, Y, R¹, R², R³, R⁴, R⁵, R⁶, R⁹ and R¹⁰ are as defined herein.

In step 1 of Scheme B, tri-(tert-butyl)-slilyloxy amine k is reacted with benzyl sulfonyl chloride b, as described above with reference to Scheme A, to form sulfonamide compound m. In certain embodiments the tri-(tert-butyl)-slilyloxy group may be replaced with other leaving groups.

In step 2, sulfonamide compound m is reacted with iodochloromethane to provide an alkenylsulfonamide compound n. This reaction may be achieved in the presence of a strong base such as an alkyl lithium reagent, using polar aprotic solvent such as THF under anhydrous conditions. In certain embodiments iodochloromethane may be replaced with other methylene reagents.

In step 3, a cyclization reaction is affected to provide oxathiazepane compound p. The cyclization may be carried out in the presence of an amine base under polar aprotic solvent conditions.

In step 4, oxathiazepane compound p is reacted with aryalkyl halide compound e to yield aralkyl oxathiazepane compound q, in the manner described above with reference to Scheme A.

Steps 5A or 5B may then be carried out by reaction of oxathiazepane compound q with reagents g and i respectively, in the manner described above with reference to Scheme A, to afford sultam compounds r and s respectively, which are compounds of formula I in accordance with the invention.

Many variations on the procedures of Scheme A and Scheme B are possible and will suggest themselves to those skilled in the art. Specific details for producing compounds of the invention are described in the Examples below.

Administration and Pharmaceutical Composition

The invention includes pharmaceutical compositions comprising at least one compound of the present invention, or an individual isomer, racemic or non-racemic mixture of isomers or a pharmaceutically acceptable salt or solvate thereof, together with at least one pharmaceutically acceptable carrier, and optionally other therapeutic and/or prophylactic ingredients.

In general, the compounds of the invention will be administered in a therapeutically effective amount by any of the accepted modes of administration for agents that serve similar utilities. Suitable dosage ranges are typically 1-500 mg daily, for example 1-100 mg daily, and most preferably 1-30 mg daily, depending upon numerous factors such as the severity of the disease to be treated, the age and relative health of the subject, the potency of the compound used, the route and form of administration, the indication towards which the administration is directed, and the preferences and experience of the medical practitioner involved. One of ordinary skill in the art of treating such diseases will be able, without undue experimentation and in reliance upon personal knowledge and the disclosure of this Application, to ascertain a therapeutically effective amount of the compounds of the present invention for a given disease.

Compounds of the invention may be administered as pharmaceutical formulations including those suitable for oral (including buccal and sub-lingual), rectal, nasal, topical, pulmonary, vaginal, or parenteral (including intramuscular, intraarterial, intrathecal, subcutaneous and intravenous) administration or in a form suitable for administration by inhalation or insufflation. A particular manner of administration is generally oral using a convenient daily dosage regimen which can be adjusted according to the degree of affliction.

A compound or compounds of the invention, together with one or more conventional adjuvants, carriers, or diluents, may be placed into the form of pharmaceutical compositions and unit dosages. The pharmaceutical compositions and unit dosage forms may be comprised of conventional ingredients in conventional proportions, with or without additional active compounds or principles, and the unit dosage forms may contain any suitable effective amount of the active ingredient commensurate with the intended daily dosage range to be employed. The pharmaceutical compositions may be employed as solids, such as tablets or filled capsules, semisolids, powders, sustained release formulations, or liquids such as solutions, suspensions, emulsions, elixirs, or filled capsules for oral use; or in the form of suppositories for rectal or vaginal administration; or in the form of sterile injectable solutions for parenteral use. Formulations containing about one (1) milligram of active ingredient or, more broadly, about 0.01 to about one hundred (100) milligrams, per tablet, are accordingly suitable representative unit dosage forms.

The compounds of the invention may be formulated in a wide variety of oral administration dosage forms. The pharmaceutical compositions and dosage forms may comprise a compound or compounds of the present invention or pharmaceutically acceptable salts thereof as the active component. The pharmaceutically acceptable carriers may be either solid or liquid. Solid form preparations include powders, tablets, pills, capsules, cachets, suppositories, and dispersible granules. A solid carrier may be one or more substances which may also act as diluents, flavouring agents, solubilizers, lubricants, suspending agents, binders, preservatives, tablet disintegrating agents, or an encapsulating material. In powders, the carrier generally is a finely divided solid which is a mixture with the finely divided active component. In tablets, the active component generally is mixed with the carrier having the necessary binding capacity in suitable proportions and compacted in the shape and size desired. The powders and tablets may contain from about one (1) to about seventy (70) percent of the active compound. Suitable carriers include but are not limited to magnesium carbonate, magnesium stearate, talc, sugar, lactose, pectin, dextrin, starch, gelatine, tragacanth, methylcellulose, sodium carboxymethylcellulose, a low melting wax, cocoa butter, and the like. The term “preparation” is intended to include the formulation of the active compound with encapsulating material as carrier, providing a capsule in which the active component, with or without carriers, is surrounded by a carrier, which is in association with it. Similarly, cachets and lozenges are included. Tablets, powders, capsules, pills, cachets, and lozenges may be as solid forms suitable for oral administration.

Other forms suitable for oral administration include liquid form preparations including emulsions, syrups, elixirs, aqueous solutions, aqueous suspensions, or solid form preparations which are intended to be converted shortly before use to liquid form preparations. Emulsions may be prepared in solutions, for example, in aqueous propylene glycol solutions or may contain emulsifying agents, for example, such as lecithin, sorbitan monooleate, or acacia. Aqueous solutions can be prepared by dissolving the active component in water and adding suitable colorants, flavors, stabilizers, and thickening agents. Aqueous suspensions can be prepared by dispersing the finely divided active component in water with viscous material, such as natural or synthetic gums, resins, methylcellulose, sodium carboxymethylcellulose, and other well known suspending agents. Solid form preparations include solutions, suspensions, and emulsions, and may contain, in addition to the active component, colorants, flavors, stabilizers, buffers, artificial and natural sweeteners, dispersants, thickeners, solubilizing agents, and the like.

The compounds of the invention may be formulated for parenteral administration (e.g., by injection, for example bolus injection or continuous infusion) and may be presented in unit dose form in ampoules, pre-filled syringes, small volume infusion or in multi-dose containers with an added preservative. The compositions may take such forms as suspensions, solutions, or emulsions in oily or aqueous vehicles, for example solutions in aqueous polyethylene glycol. Examples of oily or nonaqueous carriers, diluents, solvents or vehicles include propylene glycol, polyethylene glycol, vegetable oils (e.g., olive oil), and injectable organic esters (e.g., ethyl oleate), and may contain formulatory agents such as preserving, wetting, emulsifying or suspending, stabilizing and/or dispersing agents. Alternatively, the active ingredient may be in powder form, obtained by aseptic isolation of sterile solid or by lyophilization from solution for constitution before use with a suitable vehicle, e.g., sterile, pyrogen-free water.

The compounds of the invention may be formulated for topical administration to the epidermis as ointments, creams or lotions, or as a transdermal patch. Ointments and creams may, for example, be formulated with an aqueous or oily base with the addition of suitable thickening and/or gelling agents. Lotions may be formulated with an aqueous or oily base and will in general also containing one or more emulsifying agents, stabilizing agents, dispersing agents, suspending agents, thickening agents, or coloring agents. Formulations suitable for topical administration in the mouth include lozenges comprising active agents in a flavored base, usually sucrose and acacia or tragacanth; pastilles comprising the active ingredient in an inert base such as gelatine and glycerine or sucrose and acacia; and mouthwashes comprising the active ingredient in a suitable liquid carrier.

The compounds of the invention may be formulated for administration as suppositories. A low melting wax, such as a mixture of fatty acid glycerides or cocoa butter is first melted and the active component is dispersed homogeneously, for example, by stirring. The molten homogeneous mixture is then poured into convenient sized molds, allowed to cool, and to solidify.

The compounds of the invention may be formulated for vaginal administration. Pessaries, tampons, creams, gels, pastes, foams or sprays containing in addition to the active ingredient such carriers as are known in the art to be appropriate.

The subject compounds may be formulated for nasal administration. The solutions or suspensions are applied directly to the nasal cavity by conventional means, for example, with a dropper, pipette or spray. The formulations may be provided in a single or multidose form. In the latter case of a dropper or pipette, this may be achieved by the patient administering an appropriate, predetermined volume of the solution or suspension. In the case of a spray, this may be achieved for example by means of a metering atomizing spray pump.

The compounds of the invention may be formulated for aerosol administration, particularly to the respiratory tract and including intranasal administration. The compound will generally have a small particle size for example of the order of five (5) microns or less. Such a particle size may be obtained by means known in the art, for example by micronization. The active ingredient is provided in a pressurized pack with a suitable propellant such as a chlorofluorocarbon (CFC), for example, dichlorodifluoromethane, trichlorofluoromethane, or dichlorotetrafluoroethane, or carbon dioxide or other suitable gas. The aerosol may conveniently also contain a surfactant such as lecithin. The dose of drug may be controlled by a metered valve. Alternatively the active ingredients may be provided in a form of a dry powder, for example a powder mix of the compound in a suitable powder base such as lactose, starch, starch derivatives such as hydroxypropylmethyl cellulose and polyvinylpyrrolidine (PVP). The powder carrier will form a gel in the nasal cavity. The powder composition may be presented in unit dose form for example in capsules or cartridges of e.g., gelatine or blister packs from which the powder may be administered by means of an inhaler.

When desired, formulations can be prepared with enteric coatings adapted for sustained or controlled release administration of the active ingredient. For example, the compounds of the present invention can be formulated in transdermal or subcutaneous drug delivery devices. These delivery systems are advantageous when sustained release of the compound is necessary and when patient compliance with a treatment regimen is crucial. Compounds in transdermal delivery systems are frequently attached to an skin-adhesive solid support. The compound of interest can also be combined with a penetration enhancer, e.g., Azone (1-dodecylazacycloheptan-2-one). Sustained release delivery systems are inserted subcutaneously into the subdermal layer by surgery or injection. The subdermal implants encapsulate the compound in a lipid soluble membrane, e.g., silicone rubber, or a biodegradable polymer, e.g., polylactic acid.

The pharmaceutical preparations may be in unit dosage forms. In such form, the preparation is subdivided into unit doses containing appropriate quantities of the active component. The unit dosage form can be a packaged preparation, the package containing discrete quantities of preparation, such as packeted tablets, capsules, and powders in vials or ampoules. Also, the unit dosage form can be a capsule, tablet, cachet, or lozenge itself, or it can be the appropriate number of any of these in packaged form.

Other suitable pharmaceutical carriers and their formulations are described in Remington: The Science and Practice of Pharmacy 1995, edited by E. W. Martin, Mack Publishing Company, 19th edition, Easton, Pa. Representative pharmaceutical formulations containing a compound of the present invention are described below.

Utility

The compounds of the invention are useful for treatment of immune disorders generally.

The compounds may be used for treatment of arthritis, including rheumatoid arthritis, osteoarthritis, psoriatic arthritis, septic arthritis, spondyloarthropathies, gouty arthritis, systemic lupus erythematosus and juvenile arthritis, osteoarthritis, and other arthritic conditions.

The compounds may be used for treatment of respiratory disorders such as chronic obstructive pulmonary disease (COPD), asthma, bronchospasm, and the like.

The compounds may be used for treatment of gastrointestinal disorder (“GI disorder”) such as Irritable Bowel Syndrome (IBS), Inflammatory Bowel Disease (IBD), biliary colic and other biliary disorders, renal colic, diarrhea-dominant IBS, pain associated with GI distension, and the like.

The compounds may be used for treatment of pain conditions such as inflammatory pain; arthritic pain, surgical pain; visceral pain; dental pain; premenstrual pain; central pain; pain due to burns; migraine or cluster headaches; nerve injury; neuritis; neuralgias; poisoning; ischemic injury; interstitial cystitis; cancer pain; viral, parasitic or bacterial infection; post-traumatic injury; or pain associated with irritable bowel syndrome.

EXAMPLES

The following preparations and examples are given to enable those skilled in the art to more clearly understand and to practice the present invention. They should not be considered as limiting the scope of the invention, but merely as being illustrative and representative thereof.

Unless otherwise stated, all temperatures including melting points (i.e., MP) are in degrees celsius (° C.). It should be appreciated that the reaction which produces the indicated and/or the desired product may not necessarily result directly from the combination of two reagents which were initially added, i.e., there may be one or more intermediates which are produced in the mixture which ultimately leads to the formation of the indicated and/or the desired product. The following abbreviations may be used in the Preparations and Examples.

List of Abbreviations

• AcOH Acetic acid
• AIBN 2,2′-Azobis(2-methylpropionitrile)
• Atm. Atmosphere
• (BOC)₂O di-tent-Butyl dicarbonate
• DCM Dichloromethane/Methylene chloride
• DIAD Diisopropyl azodicarboxylate
• DIPEA Diisopropylethylamine
• DMAP 4-Dimethylaminopyridine
• DME 1,2-Dimethoxyethane
• DMF N,N-Dimethylformamide
• DMSO Dimethyl sulfoxide
• DPPF 1,1′-Bis(diphenylphosphino)ferrocene
• Et₂O Diethyl ether
• EtOH Ethanol/Ethyl alcohol
• EtOAc Ethyl acetate
• HATU 2-(1H-7-Azabenzotriazol-1-yl)-1,1,3,3-tetramethyl uronium hexafluorophosphate Methanaminium
• HBTU O-Benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate
• HOBT 1-Hydroxybenzotriazole
• HPLC High pressure liquid chromatography
• RP HPLC Reverse phase high pressure liquid chromatography
• i-PrOH Isopropanol/isopropyl alcohol
• LCMS Liquid Chromatograph/Mass Spectroscopy
• MeOH Methanol/Methyl alcohol
• MW Microwaves
• NBS N-Bromosuccinimide
• NMP 1-Methyl-2-pyrrolidinone
• PSI Pound per square inch
• r.t. Room temperature
• TBDMS tert-Butyldimethylsilyl
• TFA Trifluoroacetic acid
• THF Tetrahydrofuran
• TLC Thin layer chromatography

Preparations 1 and 2: (3R)-3-Aminobutan-1-ol and (3S)-3-Aminobutan-1-ol

Step 1 3-[[(Benzyloxy)carbonyl]amino]butanoic acid

Into a 2000-mL 4-necked round-bottom flask was placed a solution of 3-aminobutanoic acid (100 g, 969.75 mmol, 1.00 equiv) in water (1000 mL), followed by the addition of potassium hydroxide (136 g, 2.42 mol, 2.50 equiv) in several batches. To this was added benzyl chloroformate (247 g, 1.45 mol, 1.50 equiv) dropwise with stirring at 0-5° C. The resulting solution was stirred at 25° C. for 5 h. The reaction progress was monitored by LCMS. The resulting solution was extracted with 3×250 mL of dichloromethane and the aqueous layers were combined. The pH value of the water phase was adjusted to 3 with hydrogen chloride (2 mol/L). The precipitates were collected by filtration and dried to afford 102 g (44%) of 3-[[(benzyloxy)carbonyl]amino]butanoic acid as a white solid.

Step 2: Benzyl N-[(2S)-4-hydroxybutan-2-yl]carbamate and Benzyl N-[(2R)-4-hydroxybutan-2-yl]carbamate

Into a 2000-mL 3-necked round-bottom flask purged and maintained with an inert atmosphere of nitrogen was placed a solution of 3-[[(benzyloxy)carbonyl]amino]butanoic acid (102 g, 429.92 mmol, 1.00 equiv) in THF (300 mL), followed by the addition of BH₃/THF (1N) (645 mL, 1.50 equiv) dropwise with stirring at 0-5° C. The resulting solution was stirred at 40° C. for 2 h, quenched by the addition of 200 mL of methanol and concentrated under vacuum. The residue was purified on a silica gel column eluting with ethyl acetate: petroleum ether (1:2). The crude product (70 g) was purified by Prep-SFC with the following conditions (prep SFC): Column, Phenomenex Lux 5 u Cellulose-4, 2.12*25.5 um; mobile phase, CO₂ (85%), ethanol (15%); Detector, UV 254 nm. This resulted in 30 g (31.5%) of benzyl N-[(2R)-4-hydroxybutan-2-yl]carbamate as an off-white solid and 30 g (31.5%) of benzyl N-[(2S)-4-hydroxybutan-2-yl]carbamate as an off-white solid.

Step 3: (3R)-3-Aminobutan-1-ol and (3S)-3-Aminobutan-1-ol

Into a 1000-mL round-bottom flask was placed a solution of benzyl N-[(2S)-4-hydroxybutan-2-yl]carbamate (30 g, 134.4 mmol, 1.00 equiv) in methanol (500 mL) and palladium carbon (3 g, 0.10 equiv). The resulting solution was stirred at 25° C. for 12 h under an atmosphere of hydrogen. The solids were filtered out and the filtrate was concentrated under vacuum to afford 11.7 g (92%) of (3S)-3-aminobutan-1-ol as an oil. ¹H NMR (300 MHz, DMSO, ppm): δ 4.48 (3H, s), 3.47 (2H, s), 2.96 (1H, s), 1.47-1.41 (2H, q), 1.02-0.99 (3H, d); LCMS (ESI), m/z, 90 [M+H]±; measured [α]_D^20.2+11.65° (C=1.22 g/100 mL in EtOH), lit. [α]_D²°+16.3° (c=4.5 in EtOH) (J. Org. Chem. 1996, 61, 2293-2304.).

Using the above procedure, 12.0 g 12 g (94%) of (3R)-3-aminobutan-1-ol was isolated as an oil. ¹H NMR (300 MHz, DMSO, ppm): δ 4.48 (3H, s), 3.47 (2H, s), 2.96 (1H, s), 1.47-1.41 (2H, q), 1.02-0.99 (3H, d); LCMS (ESI), m/z, 90 [M+H]±; measured [α]_D^20.2 −11.1° (C=0.32 g/100 mL in EtOH), lit. [α]_D²⁵ −25° (c=1.25 in EtOH) (Tetrahedron: Asymmetry 1999, 10, 2213-2224.).

Preparation 3: (R)—N-(4-Chlorobutan-2-yl)-1-phenylmethanesulfonamide

Step 1: (R)-3-(Phenylmethylsulfonamido)butyl phenylmethanesulfonate

To a solution of (3R)-3-aminobutan-1-ol (1.0 g, 11.2 mmol) and triethylamine (3.3 mL, 23.6 mmol) in tetrahydrofuran (37 mL) at 0° C. was slowly added phenylmethanesulfonyl chloride (4.49 g, 23.6 mmol) and the reaction was stirred at room temperature for 16 hours. MTBE (100 mL) was then added and the Et₃N.HCl salt was removed by filtration. The filtrate was then concentrated to give crude (R)-3-(phenylmethylsulfonamido)butyl phenylmethanesulfonate which was used without purification. LCMS (ESI), m/z, 398 [M+H]+.

Step 2: (R)—N-(4-Chlorobutan-2-yl)-1-phenylmethanesulfonamide

To the crude (R)-3-(phenylmethylsulfonamido)butyl phenylmethanesulfonate (23.6 mmol) was added sodium chloride (984 mg, 16.8 mmol) and dimethylformamide (37 mL) and the reaction was stirred at 80° C. for 16 hours. The reaction was then diluted with EtOAc, washed with water (×2) and brine, dried with MgSO₄, concentrated and purified by silica gel column chromatography (0-50% Acetone in Heptane, 216 nM) to give (R)—N-(4-chlorobutan-2-yl)-1-phenylmethanesulfonamide (1.71 g, 6.53 mmol, 58% yield over 2 steps). LCMS (ESI), m/z, 261 [M+H]+.

Additional compounds made using the above procedure are shown in Table 1.

TABLE 1

LCMS (ESI),

Structure

Name

m/z, [M + H]+

4

(S)-N-(4-chlorobutan-2- yl)-1-phenylmethanesul- fonamide

261

5

N-(4-chloro-2-methyl- butan-2-yl)-1-phenyl- methanesulfonamide

275

6

N-(4-chlorobutyl)-1- phenylmethane- sulfonamide

261

Preparation 7: N-(2-bromoethyl)(phenyl)methanesulfonamide

K₂CO₃ (8.7 g, 62 mmol) was added into a mixture of phenylmethanesulfonyl chloride (6 g, 31 mmol) and 2-bromoethanamine hydrobromide (6.4 g, 31 mmol) in DCM (100 mL) at 0° C. And the resulting mixture was stirred at r.t. for 4 hours and left standing overnight. Upon the completion of reaction, water (100 mL) was added in and DCM phase was separated. The aqueous phase was extracted with DCM. The combined organic phase was dried over Na₂SO₄, filtered and concentrated in vacuo to provide a crude which was separated with column chromatography (silica gel with 200-300 mesh, 0 to 50% of EtOAc in petroleum ether) to provide compound N-(2-bromoethyl)(phenyl)methanesulfonamide (7.0 g, 80%) as a pale yellow solid. ¹H NMR (300 MHz, CDCl₃) δ 7.40 (m, 5H), 4.58 (m, 1H), 4.29 (s, 2H), 3.34-3.29 (m, 4H). LCMS (ESI), 300, 302 [M+Na]⁺, Br pattern found.

Preparation 8 N-(2-bromoethyl)(4-fluorophenyl)methanesulfonamide

N-(2-bromoethyl)(4-fluorophenyl)methanesulfonamide was also made using the above procedure, replacing phenylmethanesulfonyl chloride with 4-fluoro-phenylmethanesulfonyl chloride. ¹H NMR (300 MHz, CDCl₃) δ 7.43-7.38 (m, 2H), 7.13-7.07 (m, 2H), 4.62 (br s, 1H), 4.26 (s, 2H), 3.41-3.32 (m, 4H).

Preparation 9: N-(3-bromopropyl)(phenyl)methanesulfonamide

A solution of phenylmethanesulfonyl chloride (2.19 g, 10 mmol) was added into a suspension of 3-bromopropan-1-amine hydrobromide (2.19 g, 10 mmol) and Et₃N (2.02 g, 20 mmol) in THF (50 mL) at 0° C. The mixture was stirred at 0° C. for 5 min. TLC confirmed the completion of reaction. Solid was filtered out with suction, and the filtrate was concentrated to provide compound N-(3-bromopropyl)(phenyl)methanesulfonamide (2.7 g, quant.) as a pale yellow solid which was used in the next step without further purification. ¹H NMR (300 MHz, CDCl₃) δ 7.40 (m, 5H), 4.48 (m, 1H), 4.27 (s, 2H), 3.41 (t, J=6.6 Hz, 2H), 3.16 (q, 2H), 2.01 (m, 2H). LCMS (ESI), m/z, 314 and 316 [M+Na]⁺, Br pattern found.

Preparation 10: N-(3-bromopropyl)(4-fluorophenyl)methanesulfonamide

N-(3-bromopropyl)(4-fluorophenyl)methanesulfonamide was prepared using the above procedure. ¹H NMR (300 MHz, CDCl₃) δ 7.42-7.37 (m, 2H), 7.13-7.07 (m, 2H), 4.26 (m, 1H), 4.24 (s, 2H), 3.46-3.42 (m, 2H), 3.20-3.16 (m, 2H), 2.05-2.00 (m, 2H).

Preparation 11: 6-Phenyl-1,2-thiazinane 1,1-dioxide

To a solution of N-(3-bromopropyl)-1-phenylmethanesulfonamide (2.3 g, 7.9 mmol), diisopropylamine (0.28 mL, 2.0 mmol) and 1,10-phenanthroline (3.6 mg, 0.02 mmol) in tetrahydrofuran (26 mL) at −78° C. was added n-BuLi (6.8 mL, 2.5 M in hexanes) dropwise and the reaction was stirred for 16 hours. Saturated NH₄Cl was then added and the reaction was diluted with EtOAc, washed with water and brine, dried with MgSO₄, concentrated and purified by silica gel column chromatography (0-50% EtOAc/heptane) to 6-Phenyl-1,2-thiazinane 1,1-dioxide (1.3 g, 80% yield). ¹H NMR (300 MHz, DMSO-d₆) δ 7.40-7.35 (m, 5H), 6.98 (m, 1H), 4.12 (dd, 1H), 3.26-3.20 (m, 2H), 2.40-2.30 (m, 1H), 2.16-2.12 (m, 1H), 1.77-1.65 (m, 2H). LCMS (ESI), m/z, 234 [M+Na]⁺. (Reference: D. Askin, et al. Org. Lett. 2003, 4175.)

Additional compounds made using the above procedure are shown in Table 2.

TABLE 2

LCMS (ESI),

Structure

Name

m/z, [M + H]⁺

12

6-(4-fluorophenyl)-1,2-thiazinane 1,1- dioxide

230

13

5-phenylisothiazolidine 1,1-dioxide

198

14

5-(4-fluorophenyl)isothiazolidine 1,1- dioxide

216

15

(3R)-3-methyl-6-phenyl-1,2-thiazinane 1,1- dioxide

226

16

(3S)-3-methyl-6-phenyl-1,2-thiazinane 1,1- dioxide

226

17

3,3-dimethyl-6-phenyl-1,2-thiazinane 1,1- dioxide

240

18

7-phenyl-1,2-thiazepane 1,1-dioxide

226

Preparation 19: 3-Phenyl-1,4,5-oxathiazepane 4,4-dioxide

Step 1: N-(2-((Tert-butyldimethylsilyl)oxy)ethyl)-1-phenylmethanesulfonamide

To a solution of 2-((tert-butyldimethylsilyl)oxy)ethanamine (11.7 g, 66.6 mmol) and triethylamine (11.2 mL, 79.9 mmol) in tetrahydrofuran (222 mL) at 0° C. was slowly added phenylmethanesulfonyl chloride (12.7 g, 66.6 mmol) portion wise and the reaction was stirred at room temperature for 16 hours. MTBE was then added and the Et₃N.HCl salt was removed by filtration. The filtrate was then concentrated and purified by silica gel column chromatography (0-30% Acetone in heptane, 216 nM) to N-(2-((tert-butyldimethylsilyl)oxy)ethyl)-1-phenylmethanesulfonamide (17.8 g, 81% yield). LCMS (ESI), m/z, 330. [M+H]+.

Step 2: N-(2-((Tert-butyldimethylsilyl)oxy)ethyl)-1-phenylethenesulfonamid

To a solution of N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-1-phenyl-methanesulfonamide (33 g, 100.2 mmol) in tetrahydrofuran (334 mL) at −78° C. was slowly added n-BuLi (2.5 M in hexanes) (100 mL, 250 mmol) via cannula and the reaction was stirred at −78° C. was 2 hours. Chloroiodomethane (8.3 mL, 110 mmol) was then slowly added and the reaction was stirred at −78° C. for one hour, then allowed to warm to room temperature and aged for 16 hours. The reaction was then quenched with saturated NH₄Cl and extracted with dichloromethane, dried with MgSO₄, concentrated and purified by silica gel column chromatography (0-60% EtOAc in heptane) to give N-[2-[tert-butyl(dimethyl)silyl]oxyethyl]-1-phenyl-ethenesulfonamide (24 g, 70% yield). LCMS (ESI), m/z, 342. [M+H]+.

Step 3: 3-Phenyl-1,4,5-oxathiazepane 4,4-dioxide

To a solution of N-(2-((Tert-butyldimethylsilyl)oxy)ethyl)-1-phenylethenesulfonamide (717 mg, 2.1 mmol) in tetrahydrofuran (7 mL) at 0° C. was added tetrabutylammonium fluoride (1.0 M in THF) (2.2 mL, 2.2 mmol) dropwise and the reaction was stirred at room temperature for 16 hours. Saturated NH₄Cl was then added and the product was extracted with dichloromethane (×2), dried with MgSO₄, concentrated and purified by silica gel column chromatography (0-100% EtOAc in heptane) to give 3-phenyl-1,4,5-oxathiazepane 4,4-dioxide (401 mg, 84% yield). (24 g, 70% yield). LCMS (ESI), m/z, 228. [M+H]+. (Reference: P. Hansen, et al. Org. Lett. 2008, 2951).

Additional compounds made using the above procedure are shown in Table 3.

TABLE 3

LCMS (ESI),

Structure

Name

m/z, [M + H]⁺

20

(6R)-6-methyl-3- phenyl-1,4,5-oxathia- zepane 4,4-dioxide

242

21

(6S)-6-methyl-3- phenyl-1,4,5-oxathia- zepane 4,4-dioxide

242

22

(7S)-7-methyl-3- phenyl-1,4,5-oxathia- zepane 4,4-dioxide

242

23

(7R)-7-methyl-3- phenyl-1,4,5-oxathia- zepane 4,4-dioxide

242

Examples 1 and 2

(R)-1-(4-(4-((1,1-Dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone and (S)-1-(4-(4-((1,1-Dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone

Step 1: 2-(4-Bromo-2-fluorobenzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide

To a solution of 6-phenyl-1,2-thiazinane 1,1-dioxide (300 mg, 1.42 mmol) and 4-bromo-1-(bromomethyl)-2-fluorobenzene (456 mg, 1.7 mmol) in N,N-dimethylacetamide (5 mL) at 0° C. was added sodium hydride (60% in mineral oil) (68 mg, 1.85 mmol) and the reaction was stirred at room temperature for 2 hours. Water was added and the reaction was diluted with EtOAc, washed with brine, dried with MgSO₄, filtered and purified by silica gel column chromatography (0-60% EtOAc/heptane) to give 2-(4-bromo-2-fluorobenzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide (396 mg, 70% yield). LCMS (ESI), m/z, 398 [M+H]+.

Step 2: (R)-1-(4-(4-((1,1-Dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone and (S)-1-(4-(4-((1,1-Dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone

2-[(4-Bromo-2-fluoro-phenyl)methyl]-6-phenyl-thiazinane 1,1-dioxide (208 mg, 0.52 mmol), Pd(OAc)₂ (5.8 mg, 0.026 mmol), 2-dicyclohexylphosphine-2′,6′-di-iso-propoxy-1,1′-biphenyl (24.8 mg, 0.052 mmol) and cesium carbonate (254 mg, 0.78 mmol) were weighed out in a vial and the vial was purged with nitrogen. 1,4-Dioxane (2.5 mL) and 1-piperazin-1-ylethanone (100 mg, 0.78 mmol) were then added and the reaction was stirred at 80° C. for 2 hours. The reaction was then filtered through diatomaceous earth, concentrated and purified by reverse-phase HPLC to give 1-(4-(4-((1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone (210 mg, 89% yield).

The racemic mixture (150 mg) was separated by chiral SFC to give 1-(4-(4-((1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone as isolated stereoisomers in separate fractions: (ISOMER A) as a first fraction (50 mg, 33% yield) and 1-(4-(4-[1,1-d]oxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone (ISOMER B) as a second fraction (77 mg, 51% yield):

1-(4-(4-((1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone (Stereoisomer A): ¹H NMR (400 MHz, DMSO) δ 7.49-7.31 (m, 5H), 7.26 (t, J=8.8 Hz, 1H), 6.86-6.73 (m, 2H), 4.49 (dd, J=12.6, 3.2 Hz, 1H), 4.35 (q, J=14.4 Hz, 2H), 3.63-3.51 (m, 4H), 3.46 (t, J=12.9 Hz, 1H), 3.28-3.19 (m, 2H), 3.19-3.04 (m, 3H), 2.48-2.35 (m, 1H), 2.22-2.07 (m, 1H), 2.04 (s, 3H), 2.01-1.87 (m, 1H), 1.72-1.49 (m, 1H). LCMS (ESI), m/z, 446.1 [M+H]+.

1-(4-(4-((1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone (Stereoisomer B): ¹H NMR (400 MHz, DMSO) δ 7.49-7.31 (m, 5H), 7.26 (t, J=8.8 Hz, 1H), 6.86-6.73 (m, 2H), 4.49 (dd, J=12.6, 3.2 Hz, 1H), 4.35 (q, J=14.4 Hz, 2H), 3.63-3.51 (m, 4H), 3.46 (t, J=12.9 Hz, 1H), 3.28-3.19 (m, 2H), 3.19-3.04 (m, 3H), 2.48-2.35 (m, 1H), 2.22-2.07 (m, 1H), 2.04 (s, 3H), 2.01-1.87 (m, 1H), 1.72-1.49 (m, 1H). LCMS (ESI), m/z, 446.1 [M+H]+.

Examples 3 and 4

(S)-2-(2-Fluoro-4-((1-(methylsulfonyl)piperidin-4-yl)oxy)benzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide and (R)-2-(2-Fluoro-4-((1-(methylsulfonyl)piperidin-4-yl)oxy)benzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide

2-(4-bromo-2-fluorobenzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide (100 mg, 0.25 mmol), 1-methylsulfonylpiperidin-4-ol (67.2 mg, 0.38 mmol), copper(I) iodide (9.5 mg, 0.05 mmol), 3,4,7,8-tetramethyl-1,10-phenanthroline (24 mg, 0.1 mmol) and cesium carbonate (123 mg, 0.38 mmol) were weighed out in a vial and the vial was purged with nitrogen. p-Xylene (1 mL) was then added and the reaction was stirred at 135° C. for 16 hours. The reaction was then filtered through diatomaceous earth, concentrated and purified by reverse-phase HPLC to give 2-(2-fluoro-4-((1-(methylsulfonyl)piperidin-4-yl)oxy)benzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide (50.1 mg, 40% yield).

The racemic mixture (40 mg) was separated by chiral SFC to give 2-(2-fluoro-4-((1-(methylsulfonyl)piperidin-4-yl)oxy)benzyl)-6-phenyl-1,2-thiazinane 1,1-dioxide as isolated stereoisomers in separate fractions: ISOMER A as a first fraction (11.4 mg, 29% yield) and ISOMER B as a second fraction (11.6 mg, 29% yield).

1-(4-(4#1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone (Stereoisomer A): ¹H NMR (400 MHz, DMSO) δ 7.48-7.30 (m, 6H), 6.97-6.89 (m, 1H), 6.89-6.84 (m, 1H), 4.68-4.56 (m, 1H), 4.56-4.47 (m, 1H), 4.47-4.38 (m, 1H), 4.38-4.30 (m, 1H), 3.57-3.41 (m, 1H), 3.42-3.31 (m, 2H), 3.19-3.05 (m, 3H), 2.91 (s, 3H), 2.48-2.39 (m, 1H), 2.21-2.08 (m, 1H), 2.08-1.91 (m, 3H), 1.82-1.68 (m, 2H), 1.68-1.57 (m, 1H). LCMS (ESI), m/z, 497.1 [M+H]+.

1-(4-(4#1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-3-fluorophenyl)piperazin-1-yl)ethanone (Stereoisomer B): ¹H NMR (400 MHz, DMSO) δ 7.48-7.30 (m, 6H), 6.97-6.89 (m, 1H), 6.89-6.84 (m, 1H), 4.68-4.56 (m, 1H), 4.56-4.47 (m, 1H), 4.47-4.38 (m, 1H), 4.38-4.30 (m, 1H), 3.57-3.41 (m, 1H), 3.42-3.31 (m, 2H), 3.19-3.05 (m, 3H), 2.91 (s, 3H), 2.48-2.39 (m, 1H), 2.21-2.08 (m, 1H), 2.08-1.91 (m, 3H), 1.82-1.68 (m, 2H), 1.68-1.57 (m, 1H). LCMS (ESI), m/z, 497.1 [M+H]+.

Example 5

(3S)-2-[[2-Fluoro-4-[4-(1,2,4-triazol-4-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide

Step 1 (3S)-2-[(4-Bromo-2-fluoro-phenyl)methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide

(3S)-2-(4-bromo-2-fluorobenzyl)-3-methyl-6-phenyl-1,2-thiazinane 1,1-dioxide (40 g, 97 mmol, 15:85 mixture of cis/trans isomers, prepared as described in Step 1 of Example 1) was suspended in heptane (750 mL) and the suspension was heated to reflux. Ethyl acetate was slowly added until complete dissolution of the material occurred (250 mL). The solution was then subjected to a hot filtration, cooled to room temperature and store at 4° C. for 16 hours. Crystals were collected by filtration to give (3S)-2-[(4-bromo-2-fluoro-phenyl)methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide Stereoisomer A (30 g, 73 mmol, 72% yield). ¹H NMR (300 MHz, DMSO) δ 7.55-7.31 (m, 8H), 4.61-4.43 (m, 2H), 4.41-4.29 (m, 1H), 4.23-4.00 (m, 1H), 2.48-2.34 (m, 1H), 2.18-2.03 (m, 1H), 1.92-1.72 (m, 1H), 1.72-1.58 (m, 1H), 1.12-1.03 (d, J=6.8 Hz, 3H); LCMS [M+1]+=412.1.

Step 2 (3S)-2-[[2-Fluoro-4-[4-(1,2,4-triazol-4-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide

A vial was charged with (3S)-2-[(4-bromo-2-fluoro-phenyl)methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide (250 mg, 0.61 mmol), 4-(1,2,4-triazol-4-yl)piperidine hydrochloride (172 mg, 0.91 mmol), cuprous iodide (35 mg, 0.18 mmol), N,N-dimethylglycine (38 mg, 0.36 mmol) and tetrabutylphosphonium malonate (1.3 g, 1.9 mmol) and the vial was purged with nitrogen for. Dimethyl sulfoxide (3 mL) was then added and the vial was purged with nitrogen for an additional 2 minutes. The reaction mixture was then sonicated for 5 minutes and stirred at 45° C. for 20 hours. The DMSO solution was then directly purified by preparative HPLC to give (3S)-2-[[2-fluoro-4-[4-(1,2,4-triazol-4-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide Stereoisomer A (109 mg, 0.23 mmol, 37% yield) as a white solid. ¹H NMR (400 MHz, DMSO) δ 8.66-8.62 (s, 2H), 7.49-7.43 (m, 2H), 7.43-7.29 (m, 4H), 6.87-6.82 (m, 1H), 6.80-6.73 (m, 1H), 4.49-4.24 (m, 4H), 4.15-4.04 (m, 1H), 3.90-3.80 (m, 2H), 2.89-2.77 (m, 2H), 2.47-2.35 (m, 1H), 2.15-2.04 (m, 3H), 2.04-1.89 (m, 2H), 1.88-1.74 (m, 1H), 1.70-1.60 (m, 1H), 1.14-1.05 (d, J=6.9 Hz, 3H); LCMS [M+1]⁺=484.2.

Example 6

(3S)-2-[[2-fluoro-4-[4-(tetrazol-1-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide

To a solution of 1-[3-fluoro-4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2 yl]methyl]phenyl]piperidin-4-ol Stereoisomer A (200 mg, 0.46 mmol, prepared as described in Example 5), tetrazole (36 mg, 0.51 mmol) and triphenylphosphine (135 mg, 0.51 mmol) in dichloromethane (2.5 mL) was added diisopropyl azodicarboxylate (103 mg, 0.51 mmol) dropwise and the reaction was stirred at r.t. for 16 hours. The reaction was partitioned between water and dichloromethane and the organic layer was concentrated and purified by preparative HPLC to give (3S)-2-[[2-fluoro-4-[4-(tetrazol-1-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide Stereoisomer A (57.4 mg, 0.12 mmol, 26% yield) as a white solid. ¹H NMR (400 MHz, DMSO) δ 8.99-8.96 (s, 1H), 7.49-7.43 (m, 2H), 7.43-7.29 (m, 4H), 6.89-6.82 (m, 1H), 6.82-6.75 (m, 1H), 5.18-5.07 (m, 1H), 4.50-4.36 (m, 2H), 4.33-4.25 (m, 1H), 4.16-4.03 (m, 1H), 3.87-3.76 (m, 2H), 3.10-2.98 (m, 2H), 2.47-2.37 (m, 1H), 2.31-2.23 (m, 2H), 2.19-2.04 (m, 3H), 1.89-1.73 (m, 1H), 1.70-1.59 (m, 1H), 1.13-1.06 (d, J=6.8 Hz, 3H); LCMS [M+1]⁺=485.2.

Example 7

(3S)-2-[[2-Fluoro-4-[4-(1,2,4-oxadiazol-3-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide

Step 1 1-[3-fluoro-4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]phenyl]-N′-hydroxy-piperidine-4-carboxamidine

To s solution of 1-[3-fluoro-4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]phenyl]-piperidine-4-carbonitrile Stereoisomer A (1.37 g, 3.12 mmol, prepared as described in Example 5) in ethanol (15 mL) was added hydroxylamine (50 mass % in water, 0.29 mL, 9.4 mmol) and the reaction was stirred at 60° C. for 2 hours. The solution was concentrated and purified by preparative HPLC to give 1-[3-fluoro-4-[[(3S,6R)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]phenyl]-N′-hydroxy-piperidine-4-carboxamidine Stereoisomer A (1.1 g, 75% yield) as a white solid. ¹H NMR (400 MHz, DMSO) δ 8.82-8.76 (s, 1H), 7.48-7.43 (m, 2H), 7.42-7.33 (m, 3H), 7.32-7.26 (m, 1H), 6.82-6.76 (m, 1H), 6.72-6.65 (m, 1H), 5.36-5.26 (s, 2H), 4.49-4.42 (m, 1H), 4.42-4.36 (m, 1H), 4.31-4.23 (m, 1H), 4.15-4.01 (m, 1H), 3.80-3.67 (m, 2H), 2.72-2.59 (m, 2H), 2.46-2.36 (m, 1H), 2.21-2.04 (m, 2H), 1.84-1.74 (m, 3H), 1.73-1.57 (m, 3H), 1.12-1.04 (d, J=6.8 Hz, 3H); LCMS [M+1]⁺=475.2.

Step 2 (3S)-2-[[2-Fluoro-4-[4-(1,2,4-oxadiazol-3-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide

A solution of 1-[3-fluoro-4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]phenyl]-N′-hydroxy-piperidine-4-carboxamidine Stereoisomer A (150 mg, 0.32 mmol) in triethyl orthoformate (2 mL) was heated to 100° C. for 1 hour. 2 drops of trifluoroacetic acid were then added and the reaction was stirred at 100° C. for 1 hour. The solution was then concentrated and purified by preparative HPLC to give (3S)-2-[[2-fluoro-4-[4-(1,2,4-oxadiazol-3-yl)-1-piperidyl]phenyl]methyl]-3-methyl-6-phenyl-thiazinane 1,1-dioxide Stereoisomer A (31.8 mg, 21% yield). ¹H NMR (400 MHz, DMSO) δ 9.53-9.49 (s, 1H), 7.49-7.43 (m, 2H), 7.43-7.35 (m, 3H), 7.35-7.29 (m, 1H), 6.85-6.79 (m, 1H), 6.77-6.69 (m, 1H), 4.50-4.36 (m, 2H), 4.32-4.23 (m, 1H), 4.15-4.02 (m, 1H), 3.81-3.69 (m, 2H), 3.13-3.01 (m, 1H), 2.97-2.83 (m, 2H), 2.46-2.37 (m, 1H), 2.14-1.97 (m, 3H), 1.89-1.70 (m, 3H), 1.70-1.59 (m, 1H), 1.13-1.05 (d, J=6.8 Hz, 3H); LCMS [M+1]⁺=485.2.

Example 8 4-(((3S)-3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-N-(tetrahydro-2H-pyran-4-yl)benzamide

Step 1 Methyl (S)-methyl 4-((3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)benzoate

To a solution of (S)-3-methyl-6-phenyl-1,2-thiazinane 1,1-dioxide (20 g, 88.9 mmol) and methyl 4-(bromomethyl)benzoate (22.4 g, 97.6 mmol) in N,N-dimethylformamide (295 mL) at 0° C. was added sodium hydride (60% in mineral oil, 4.6 g, 115 mmol) in small portions and the reaction was stirred at room temperature for 3 hours. Water (500 mL) was then added and the precipitate was collected by filtration to give crude methyl (S)-methyl 4-((3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)benzoate.

Step 2 (S)-4-((3-Methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)benzoic acid

To a solution of crude methyl (S)-methyl 4-((3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)benzoate in tetrahydrofuran (300 mL) and water (100 mL) was added lithium hydroxide (21.3 g, 890 mmol) and the reaction was stirred at room temperature for 16 hours. Sodium hydroxide (1N in water, 100 mL) and water (200 mL) were then added to the reaction and the solution was washed with ethyl acetate. The aqueous layer was then acidified to pH=1 with concentrated hydrochloric acid and the precipitate was collected by filtration and dried under vacuum to give 33 grams of crude (S)-4-((3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)benzoic acid (85:15 mixture of trans:cis isomers).

Step 3 4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]benzoic acid

The crude mixture of diastereomers was dissolved in boiling acetonitrile (500 mL), subjected to a hot filtration and then cooled to room temperature and stored at 4° C. for 16 hours. Crystals were collected by filtration to give 4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]benzoic acid Stereoisomer A (6 g, 16.6 mmol, 19% yield). ¹H NMR (400 MHz, DMSO) δ 12.99-12.69 (s, 1H), 7.98-7.87 (m, 2H), 7.55-7.43 (m, 4H), 7.43-7.33 (m, 3H), 4.67-4.55 (m, 1H), 4.50-4.36 (m, 2H), 4.20-4.05 (m, 1H), 2.47-2.37 (m, 2H), 2.19-2.06 (m, 1H), 1.91-1.76 (m, 1H), 1.72-1.61 (m, 1H), 1.11-1.01 (d, J=6.8 Hz, 3H); LCMS [M+1]⁺=360.1.

Step 4 4-(((3S)-3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-N-(tetrahydro-2H-pyran-4-yl)benzamide

To a solution of 4-[[(3S)-3-methyl-1,1-dioxo-6-phenyl-thiazinan-2-yl]methyl]benzoic acid Stereoisomer A (75 mg, 0.21 mmol), tetrahydropyran-4-amine (64 mg, 0.63 mmol) and triethylamine (0.12 mL, 0.83 mmol) in N,N-dimethylformamide (1.5 mL) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (121 mg, 0.31 mmol) and the reaction was stirred at room temperature for 2 hours. The reaction was then partitioned between dichloromethane and saturated sodium bicarbonate in water. The organic layer was separated, concentrated and purified by preparative HPLC to give 4-(((3S)-3-methyl-1,1-dioxido-6-phenyl-1,2-thiazinan-2-yl)methyl)-N-(tetrahydro-2H-pyran-4-yl)benzamide Stereoisomer A (66.4 mg, 0.15 mmol, 72% yield). ¹H NMR (400 MHz, DMSO) δ 8.27-8.19 (d, J=7.7 Hz, 1H), 7.85-7.77 (m, 2H), 7.50-7.43 (m, 4H), 7.43-7.34 (m, 3H), 4.64-4.53 (m, 1H), 4.47-4.33 (m, 2H), 4.18-4.06 (m, 1H), 4.06-3.93 (m, 1H), 3.91-3.81 (m, 2H), 3.46-3.33 (m, 2H), 2.48-2.37 (m, 1H), 2.17-2.08 (m, 1H), 1.92-1.69 (m, 3H), 1.70-1.50 (m, 3H), 1.11-1.02 (d, J=6.9 Hz, 3H); LCMS [M+1]⁺=443.2.

The above compounds of Examples 1-8, together with additional compounds made using the above procedures, are shown in Table 4 below, together with RORc IC₅₀ (micromolar) and proton NMR data for selected compounds. Structures shown in table 4 with a ‘waved line” bond () associated with a chiral center represent compounds for which stereoisomers of the compound have been isolated or synthesized, but for which specific stereochemistry of the chiral center has not been definitely identified.

TABLE 4

Structure

Name

Proton NMR

IC₅₀

 1

  Stereoisomer A

1-(4-(4-((1,1- Dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)-30 fluorophenyl)piper- azin-1-yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.31 (m, 5H), 7.26 (t, J = 8.8 Hz, 1H), 6.86- 6.73 (m, 2H), 4.49 (dd, J = 12.6, 3.2 Hz, 1H), 4.35 (q, J = 14.4 Hz, 2H), 3.63-3.51 (m, 4H), 3.46 (t, J = 12.9 Hz, 1H), 3.28-3.19 (m, 2H), 3.19-3.04 (m, 3H), 2.48- 2.35 (m, 1H), 2.22-2.07 (m, 1H), 2.04 (s, 3H), 2.01-1.87 (m, 1H), 1.72-1.49 (m, 1H)

0.247

 2

  Stereoisomer B

1-(4-(4-((1,1- Dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)-3- fluorophenyl)piper- azin-1-yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.31 (m, 5H), 7.26 (t, J = 8.8 Hz, 1H), 6.86- 6.73 (m, 2H), 4.49 (dd, J = 12.6, 3.2 Hz, 1H), 4.35 (q, J = 14.4 Hz, 2H), 3.63-3.51 (m, 4H), 3.46 (t, J = 12.9 Hz, 1H), 3.28-3.19 (m, 2H), 3.19-3.04 (m, 3H), 2.48- 2.35 (m, 1H), 2.22-2.07 (m, 1H), 2.04 (s, 3H), 2.01-1.87 (m, 1H), 1.72-1.49 (m, 1H).

0.157

 3

  Stereoisomer A

2-(2-Fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1-

¹H NMR (400 MHz, DMSO) δ 7.48-7.30 (m, 6H), 6.97- 6.89 (m, 1H), 6.89-6.84 (m, 1H), 4.68-4.56 (m, 1H), 4.56-4.47 (m, 1H), 4.47- 4.38 (m, 1H), 4.38-4.30 (m, 1H), 3.57-3.41 (m, 1H), 3.42-3.31 (m, 2H), 3.19- 3.05 (m, 3H), 2.91 (s, 3H), 2.48-2.39 (m, 1H), 2.21- 2.08 (m, 1H), 2.08-1.91 (m, 3H), 1.82-1.68 (m, 2H), 1.68-1.57 (m, 1H)

0.086

 4

  Stereoisomer B

2-(2-Fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.48-7.30 (m, 6H), 6.97- 6.89 (m, 1H), 6.89-6.84 (m, 1H), 4.68-4.56 (m, 1H), 4.56-4.47 (m, 1H), 4.47- 4.38 (m, 1H), 4.38-4.30 (m, 1H), 3.57-3.41 (m, 1H), 3.42-3.31 (m, 2H), 3.19- 3.05 (m, 3H), 2.91 (s, 3H), 2.48-2.39 (m, 1H), 2.21- 2.08 (m, 1H), 2.08-1.91 (m, 3H), 1.82-1.68 (m, 2H), 1.68-1.57 (m, 1H)

0.037

 5

  Stereoisomer A

1-{4-[4-(1,1- Dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.53-7.32 (m, 5H), 7.29- 7.22 (m, 1H), 6.85-6.80 (m, 1H), 6.80-6.75 (m, 1H), 4.54-4.44 (m, 1H), 4.38 (d, J = 14.4 Hz, 1H), 4.32 (d, J = 14.3 Hz, 1H), 3.63-3.52 (m, 4H), 3.52-3.40 (m, 1H), 3.28-3.20 (m, 2H), 3.20- 3.04 (m, 3H), 2.47-2.36 (m, 1H), 2.18-2.07 (m, 1H), 2.04 (s, 3H), 2.02-1.91 (m, 1H), 1.71-1.56 (m, 1H).

0.247

 6

  Stereoisomer B

1-{4-[4-(1,1- Dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.32 (m, 5H), 7.30- 7.21 (m, 1H), 6.84-6.80 (m, 1H), 6.80-6.75 (m, 1H), 4.55-4.44 (m, 1H), 4.38 (d, J = 14.2 Hz, 1H), 4.32 (d, J = 14.4 Hz, 1H), 3.60-3.52 (m, 4H), 3.52-3.40 (m, 1H), 3.26-3.19 (m, 2H), 3.19- 3.04 (m, 3H), 2.48-2.36 (m, 1H), 2.18-2.06 (m, 1H), 2.04 (s, 3H), 2.01-1.92 (m, 1H), 1.69-1.57 (m, 1H).

0.157

 7

1-(4-{3-Fluoro-4- [6-(4-fluoro- phenyl)-1,1-dioxo- [1,2]thiazinan-2- ylmethyl]-phenyl}- piperazin-1-yl)- ethanone

¹H NMR (400 MHz, DMSO) δ 7.55-7.43 (m, 2H), 7.32- 7.15 (m, 3H), 6.87-6.74 (m, 2H), 4.54 (dd, J = 12.6, 3.2 Hz, 1H), 4.34 (q, J = 14.4 Hz, 2H), 3.62-3.52 (m, 4H), 3.45 (t, J = 12.9 Hz, 1H), 3.27-3.19 (m, 2H), 3.19- 3.04 (m, 3H), 2.48-2.29 (m, 1H), 2.19-2.08 (m, 1H), 2.04 (s, 3H), 2.02-1.85 (m, 1H), 1.70-1.52 (m, 1H).

0.443

 8

1-{4-[4-(1,1- Dioxo-5-phenyl- isothiazolidin-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.52-7.35 (m, 5H), 7.26 (t, J = 8.6 Hz, 1H), 6.79 (d, J = 11.0 Hz, 2H), 4.65-4.52 (m, 1H), 4.20 (d, J = 14.5 Hz, 1H), 4.06 (d, J = 14.4 Hz, 1H), 3.64-3.50 (m, 4H), 3.29-3.08 (m, 6H), 2.63- 2.52 (m, 1H), 2.49-2.42 (m, 1H), 2.04 (s, 3H).

4.9 

 9

1-(4-{3-Fluoro-4- [5-(4-fluoro- phenyl)-1,1-dioxo- isothiazolidin-2- ylmethyl]-phenyl}- piperazin-1-yl)- ethanone

¹H NMR (400 MHz, DMSO) δ 7.50 (dd, J = 8.7, 5.5 Hz, 2H), 7.26 (t, J = 8.8 Hz, 3H), 6.79 (d, J = 11.2 Hz, 2H), 4.62 (dd, J = 10.9, 7.9 Hz, 1H), 4.20 (d, J = 14.4 Hz, 1H), 4.06 (d, J = 14.4 Hz, 1H), 3.62-3.51 (m, 4H), 3.29-3.09 (m, 6H), 2.64- 2.52 (m, 1H), 2.48-2.39 (m, 1H), 2.04 (s, 3H).

7.6 

 10

1-{4-[4-(1,1- Dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.31 (m, 5H), 7.26 (t, J = 8.8 Hz, 1H), 6.86- 6.73 (m, 2H), 4.49 (dd, J = 12.6, 3.2 Hz, 1H), 4.35 (q, J = 14.4 Hz, 2H), 3.63-3.51 (m, 4H), 3.46 (t, J = 12.9 Hz, 1H), 3.28-3.19 (m, 2H), 3.19-3.04 (m, 3H), 2.48- 2.35 (m, 1H), 2.22-2.07 (m, 1H), 2.04 (s, 3H), 2.01-1.87 (m, 1H), 1.72-1.49 (m, 1H).

0.149

 11

  Stereoisomer A

1-(4-{3-Fluoro-4- [6-(4-fluoro- phenyl)-1,1-dioxo- [1,2]thiazinan-2- ylmethyl]-phenyl}- piperazin-1-yl)- ethanone

¹H NMR (400 MHz, DMSO) δ 7.54-7.44 (m, 2H), 7.30- 7.19 (m, 3H), 6.84-6.74 (m, 2H), 4.59-4.48 (m, 1H), 4.38 (d, J = 14.4 Hz, 1H), 4.31 (d, J = 14.4 Hz, 1H), 3.64-3.52 (m, 4H), 3.52- 3.37 (m, 1H), 3.26-3.19 (m, 2H), 3.19-3.07 (m, 3H), 2.48-2.30 (m, 1H), 2.18- 2.07 (m, 1H), 2.04 (s, 3H), 2.02-1.86 (m, 1H), 1.71- 1.57 (m, 1H).

0.125

 12

  Stereoisomer B

1-(4-{3-Fluoro-4- [6-(4-fluoro- phenyl)-1,1-dioxo- [1,2]thiazinan-2- ylmethyl]-phenyl}- piperazin-1-yl)- ethanone

¹H NMR (400 MHz, DMSO) δ 7.54-7.43 (m, 2H), 7.32- 7.17 (m, 3H), 6.85-6.73 (m, 2H), 4.59-4.48 (m, 1H), 4.38 (d, J = 14.4 Hz, 1H), 4.31 (d, J = 14.4 Hz, 1H), 3.61-3.52 (m, 4H), 3.52- 3.38 (m, 1H), 3.25-3.19 (m, 2H), 3.19-3.02 (m, 3H), 2.48-2.30 (m, 1H), 2.17- 2.07 (m, 1H), 2.04 (s, 3H), 2.02-1.87 (m, 1H), 1.69- 1.57 (m, 1H).

0.241

 13

  Stereoisomer A

1-{4-[4-(3,3- Dimethyl-1,1- dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.53-7.34 (m, 6H), 6.86- 6.77 (m, 1H), 6.77-6.66 (m, 1H), 4.57-4.48 (m, 1H), 4.43 (d, J = 17.5 Hz, 1H), 4.19 (d, J = 17.5 Hz, 1H), 3.61-3.51 (m, 4H), 3.23- 3.16 (m, 2H), 3.16-3.07 (m, 2H), 2.77-2.56 (m, 1H), 2.20-2.06 (m, 1H), 2.04 (s, 3H), 2.01-1.92 (m, 1H), 1.88-1.73 (m, 1H), 1.42 (s, 3H), 1.14 (s, 3H).

0.142

 14

  Stereoisomer B

1-{4-[4-(3,3- Dimethyl-1,1- dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.54-7.35 (m, 6H), 6.86- 6.78 (m, 1H), 6.78-6.66 (m, 1H), 4.58-4.47 (m, 1H), 4.43 (d, J = 17.4 Hz, 1H), 4.19 (d, J = 17.5 Hz, 1H), 3.61-3.51 (m, 4H), 3.24- 3.16 (m, 2H), 3.16-3.07 (m, 2H), 2.77-2.58 (m, 1H), 2.17-2.07 (m, 1H), 2.04 (s, 3H), 2.01-1.92 (m, 1H), 1.86-1.75 (m, 1H), 1.42 (s, 3H), 1.14 (s, 3H).

1.9 

 15

  Stereoisomer A

1-{4-[4-(1,1- Dioxo-7-phenyl- [1,2]thiazepan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.43-7.29 (m, 5H), 7.29- 7.21 (m, 1H), 6.86-6.75 (m, 2H), 4.58 (d, J = 15.2 Hz, 1H), 4.45-4.34 (m, 1H), 4.27 (d, J = 15.2 Hz, 1H), 3.59-3.52 (m, 4H), 3.53- 3.40 (m, 1H), 3.26-3.18 (m, 2H), 3.18-3.09 (m, 2H), 3.02-2.84 (m, 1H), 2.22- 2.07 (m, 1H), 2.07-1.94 (m, 6H), 1.86-1.67 (m, 1H), 1.67-1.47 (m, 1H).

0.011

 16

  Stereoisomer B

1-{4-[4-(1,1- Dioxo-7-phenyl- [1,2]thiazepan-2- ylmethyl)-3-fluoro- phenyl]-piperazin- 1-yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 7.44-7.29 (m, 5H), 7.29- 7.21 (m, 1H), 6.88-6.72 (m, 2H), 4.58 (d, J = 15.2 Hz, 1H), 4.45-4.33 (m, 1H), 4.27 (d, J = 15.1 Hz, 1H), 3.59-3.52 (m, 4H), 3.52- 3.42 (m, 1H), 3.25-3.18 (m, 2H), 3.18-3.10 (m, 2H), 3.01-2.83 (m, 1H), 2.23- 2.07 (m, 1H), 2.07-1.95 (m, 6H), 1.86-1.69 (m, 1H), 1.68-1.46 (m, 1H).

0.032

 17

  Stereoisomer A

1-{4-[3-Fluoro-4- ((3S)-3-methyl-1,1- dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.43 (m, 2H), 7.43- 7.28 (m, 4H), 6.81 (d, J = 8.8 Hz, 1H), 6.74 (d, J = 13.9 Hz, 1H), 4.52-4.44 (m, 1H), 4.41 (d, J = 17.0 Hz, 1H), 4.28 (d, J = 17.1 Hz, 1H), 4.18-4.00 (m, 1H), 3.63- 3.51 (m, 4H), 3.26-3.15 (m, 2H), 3.15-3.02 (m, 2H), 2.47-2.30 (m, 1H), 2.15- 2.05 (m, 1H), 2.03 (s, 3H), 1.92-1.71 (m, 1H), 1.71- 1.54 (m, 1H), 1.08 (d, J = 6.8 Hz, 3H).

0.016

 18

  Stereoisomer B

1-{4-[3-Fluoro-4- ((3S)-3-methyl-1,1- dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.53-7.34 (m, 5H), 7.32- 7.24 (m, 1H), 6.87-6.74 (m, 2H), 4.48-4.30 (m, 3H), 3.60-3.48 (m, 5H), 3.25- 3.18 (m, 2H), 3.18-3.11 (m, 2H), 2.81-2.61 (m, 1H), 2.17-1.95 (m, 5H), 1.67- 1.53 (m, 1H), 1.34 (d, J = 7.1 Hz, 3H).

0.047

 19

  Stereoisomer A

1-{4-[3-Fluoro-4- ((3R)-3-methyl-1,1- dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.43 (m, 2H), 7.43- 7.25 (m, 4H), 6.81 (d, J = 9.0 Hz, 1H), 6.74 (d, J = 13.8 Hz, 1H), 4.52-4.44 (m, 1H), 4.41 (d, J = 17.1 Hz, 1H), 4.28 (d, J = 16.6 Hz, 1H), 4.17-4.01 (m, 1H), 3.62- 3.50 (m, 4H), 3.23-3.15 (m, 2H), 3.15-3.07 (m, 2H), 2.48-2.29 (m, 1H), 2.15- 2.05 (m, 1H), 2.03 (s, 3H), 1.90-1.73 (m, 1H), 1.70- 1.57 (m, 1H), 1.08 (d, J = 6.7 Hz, 3H).

2.8 

 20

  Stereoisomer B

1-{4-[3-Fluoro-4- ((3R)-3-methyl-1,1- dioxo-6-phenyl- [1,2]thiazinan-2- ylmethyl)-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.50-7.34 (m, 5H), 7.32- 7.24 (m, 1H), 6.86-6.73 (m, 2H), 4.45-4.32 (m, 3H), 3.63-3.51 (m, 5H), 3.26- 3.19 (m, 2H), 3.19-3.09 (m, 2H), 2.83-2.60 (m, 1H), 2.18-1.94 (m, 5H), 1.70- 1.53 (m, 1H), 1.34 (d, J = 7.1 Hz, 3H).

0.026

 21

1-{4-[4-(4,4- Dioxo-3-phenyl- [1,4,5]oxathiazepan- 5-ylmethyl)-3- fluoro-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.43-7.35 (m, 5H), 7.30- 7.22 (m, 1H), 6.85-6.76 (m, 2H), 4.79-4.70 (m, 1H), 4.69-4.58 (d, J = 14.8 Hz, 1H), 4.27-4.07 (m, 3H), 4.05-3.97 (m, 1H), 3.90- 3.79 (m, 1H), 3.77-3.64 (m, 1H), 3.60-3.51 (m, 4H), 3.26-3.19 (m, 2H), 3.19- 3.11 (m, 2H), 3.05-2.94 (m, 1H), 2.04 (s, 3H).

0.209

 22

  Stereoisomer A

1-{4-[4-(4,4- Dioxo-3-phenyl- [1,4,5]oxathiazepan- 5-ylmethyl)-3- fluoro-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.43-7.35 (m, 5H), 7.30- 7.22 (m, 1H), 6.85-6.76 (m, 2H), 4.79-4.70 (m, 1H), 4.69-4.58 (d, J = 14.8 Hz, 1H), 4.27-4.07 (m, 3H), 4.05-3.97 (m, 1H), 3.90- 3.79 (m, 1H), 3.77-3.64 (m, 1H), 3.60-3.51 (m, 4H), 3.26-3.19 (m, 2H), 3.19- 3.11 (m, 2H), 3.05-2.94 (m, 1H), 2.04-2.01 (s, 3H).

0.751

 23

  Stereoisomer B

1-{4-[4-(4,4- Dioxo-3-phenyl- [1,4,5]oxathiazepan- 5-ylmethyl)-3- fluoro-phenyl]- piperazin-1-yl}- ethanone

¹H NMR (400 MHz, DMSO) δ 7.46-7.34 (m, 5H), 7.33- 7.18 (m, 1H), 6.88-6.74 (m, 2H), 4.79-4.72 (m, 1H), 4.68-4.57 (d, J = 14.8 Hz, 1H), 4.29-4.06 (m, 3H), 4.06-3.96 (m, 1H), 3.90- 3.77 (m, 1H), 3.77-3.62 (m, 1H), 3.61-3.51 (m, 4H), 3.27-3.18 (m, 2H), 3.18- 3.10 (m, 2H), 3.05-2.92 (m, 1H), 2.04-2.00 (s, 3H).

0.045

 24

  Stereoisomer A

1-(4-(3-fluoro-4- (((6S)-6-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.48-7.28 (m, 6H), 6.89- 6.73 (m, 2H), 4.61-4.50 (m, 2H), 4.34-4.26 (d, J = 14.7 Hz, 1H), 4.21-4.13 (m, 1H), 4.13-4.05 (m, 1H), 4.00- 3.89 (m, 1H), 3.82-3.70 (m, 1H), 3.61-3.51 (m, 4H), 3.44-3.33 (m, 1H), 3.28- 3.21 (m, 2H), 3.21-3.13 (m, 2H), 2.04 (s, 3H), 0.96-0.90 (d, J = 6.5 Hz, 3H).

0.182

 25

  Stereoisomer B

1-(4-(3-fluoro-4- (((6S)-6-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.45-7.35 (m, 5H), 7.34- 7.28 (m, 1H), 6.82-6.76 (m, 1H), 6.76-6.67 (m, 1H), 4.89-4.81 (m, 1H), 4.51- 4.42 (d, J = 17.0 Hz, 1H), 4.41-4.26 (m, 2H), 4.19- 4.10 (d, J = 16.8 Hz, 1H), 4.01-3.92 (dd, J = 13.6, 3.2 Hz, 1H), 3.91-3.82 (m, 1H), 3.82-3.72 (m, 1H), 3.60- 3.51 (m, 4H), 3.22-3.16 (m, 2H), 3.16-3.08 (m, 2H), 2.03 (s, 3H), 0.93-0.84 (d, J = 6.7 Hz, 3H).

0.032

 26

  Stereoisomer A

1-(4-(3-fluoro-4- (((6R)-6-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.46-7.35 (m, 5H), 7.35- 7.27 (m, 1H), 6.83-6.76 (m, 1H), 6.76-6.69 (dd, J = 14.0, 2.4 Hz, 1H), 4.87- 4.81 (m, 1H), 4.50-4.42 (d, J = 17.0 Hz, 1H), 4.42-4.35 (m, 1H), 4.35-4.27 (m, 1H), 4.18-4.09 (d, J = 16.8 Hz, 1H), 4.00-3.92 (dd, J = 13.6, 3.2 Hz, 1H), 3.91- 3.82 (m, 1H), 3.82-3.72 (m, 1H), 3.61-3.50 (m, 4H), 3.22-3.16 (m, 2H), 3.16- 3.03 (m, 2H), 2.03 (s, 3H), 0.91-0.84 (d, J = 6.8 Hz, 3H).

2.  

 27

  Stereoisomer B

1-(4-(3-fluoro-4- (((6R)-6-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.46-7.28 (m, 6H), 6.88- 6.74 (m, 2H), 4.64-4.49 (m, 2H), 4.34-4.24 (d, J = 14.7 Hz, 1H), 4.22-4.13 (dd, J = 13.0, 6.5 Hz, 1H), 4.13- 4.05 (m, 1H), 4.01-3.89 (m, 1H), 3.81-3.69 (m, 1H), 3.61-3.51 (m, 4H), 3.47- 3.32 (m, 1H), 3.28-3.21 (m, 2H), 3.21-3.13 (m, 2H), 2.03 (s, 3H), 0.98-0.87 (d, J = 6.3 Hz, 3H).

0.188

 28

  Stereoisomer A

1-(4-(3-fluoro-4- (((7S)-7-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.48-7.34 (m, 5H), 7.29- 7.22 (m, 1H), 6.86-6.74 (m, 2H), 4.80-4.71 (m, 1H), 4.69-4.58 (d, J = 15.1 Hz, 1H), 4.37-4.26 (d, J = 15.0 Hz, 1H), 4.22-3.97 (m, 3H), 3.61-3.51 (m, 4H), 3.39- 3.30 (m, 1H), 3.25-3.20 (m, 2H), 3.20-3.09 (m, 2H), 2.81-2.69 (m, 1H), 2.02 (s, 2H), 1.22-1.11 (d, J = 6.1 Hz, 3H).

0.104

 29

  Stereoisomer B

1-(4-(3-fluoro-4- (((7S)-7-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.45-7.36 (m, 6H), 7.28- 7.22 (m, 1H), 6.84-6.73 (m, 2H), 4.78-4.67 (m, 1H), 4.68-4.57 (d, J = 14.8 Hz, 1H), 4.47-4.30 (m, 2H), 4.30-4.20 (d, J = 14.8 Hz, 1H), 3.90-3.78 (dd, J = 13.9, 3.6 Hz, 1H), 3.62- 3.53 (m, 4H), 3.52-3.43 (m, 1H), 3.24-3.18 (m, 2H), 3.18-3.09 (m, 2H), 3.01- 2.88 (m, 1H), 2.03 (s, 3H), 1.18-1.08 (d, J = 6.6 Hz, 3H).

0.024

 30

  Stereoisomer A

1-(4-(3-fluoro-4- (((7R)-7-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.46-7.35 (m, 5H), 7.29- 7.21 (m, 1H), 6.86-6.75 (m, 2H), 4.81-4.70 (m, 1H), 4.70-4.57 (d, J = 15.1 Hz, 1H), 4.36-4.25 (d, J = 14.8 Hz, 1H), 4.23-3.99 (m, 3H), 3.60-3.52 (m, 4H), 3.39- 3.30 (m, 1H), 3.27-3.19 (m, 2H), 3.19-3.12 (m, 2H), 2.81-2.69 (m, 1H), 2.03 (s, 3H), 1.20-1.12 (d, J = 6.2 Hz, 3H).

0.107

 31

  Stereoisomer B

1-(4-(3-fluoro-4- (((7R)-7-methyl- 4,4-dioxido-3- phenyl-1,4,5- oxathiazepan-5- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.47-7.33 (m, 5H), 7.29- 7.21 (m, 1H), 6.84-6.74 (m, 2H), 4.77-4.68 (m, 1H), 4.68-4.56 (d, J = 14.8 Hz, 1H), 4.46-4.31 (m, 2H), 4.31-4.20 (d, J = 14.7 Hz, 1H), 3.88-3.78 (m, 1H), 3.63-3.53 (m, 4H), 3.53- 3.41 (m, 1H), 3.26-3.19 (m, 2H), 3.19-3.08 (m, 2H), 3.00-2.87 (m, 1H), 2.03 (s, 3H), 1.17-1.09 (d, J = 6.2 Hz, 3H).

0.717

 32

  Stereoisomer A

2-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)- (3S)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.50-7.43 (m, 2H), 7.43- 7.31 (m, 3H), 7.28-7.18 (m, 2H), 6.99-6.87 (m, 2H), 4.51-4.40 (d, J = 16.5 Hz, 1H), 4.40-4.30 (m, 1H), 4.27-4.15 (d, J = 16.5 Hz, 1H), 4.15-3.89 (m, 1H), 3.62-3.49 (m, 4H), 3.19- 3.09 (m, 2H), 3.09-3.00 (m, 2H), 2.46-2.32 (m, 1H), 2.13-2.05 (m, 1H), 2.01 (s, 3H), 1.93-1.71 (m, 1H), 1.71-1.57 (m, 1H), 1.14- 1.01 (d, J = 6.9 Hz, 3H).

0.017

 33

  Stereoisomer B

2-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)- (3S)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

0.013

 34

  Stereoisomer A

2-[6-(1- Methanesulfonyl- piperidin-4-yloxy)- pyridin-3- ylmethyl]-(3S)-3- methyl-6-phenyl- [1,2]thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 8.17-8.10 (d, J = 2.3 Hz, 1H), 7.76-7.66 (m, 1H), 7.51-7.44 (m, 2H), 7.44- 7.32 (m, 3H), 6.85-6.74 (d, J = 8.5 Hz, 1H), 5.24-4.98 (m, 1H), 4.56-4.36 (m, 2H), 4.36-4.18 (m, 1H), 4.17- 3.94 (m, 1H), 3.46-3.31 (m, 2H), 3.20-3.05 (m, 2H), 2.96-2.85 (s, 3H), 2.46- 2.26 (m, 1H), 2.18-1.96 (m, 3H), 1.95-1.57 (m, 4H), 1.23-1.02 (d, J = 6.8 Hz, 3H).

0.686

 35

  Stereoisomer B

(3S,6S)-2-[6-(1- Methanesulfonyl- piperidin-4-yloxy)- pyridin-3- ylmethyl]-(3S)-3- methyl-6-phenyl- [1,2]thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 8.17-8.12 (d, J = 2.4 Hz, 1H), 7.76-7.69 (m, 1H), 7.51-7.44 (m, 2H), 7.43- 7.34 (m, 3H), 6.90-6.82 (d, J = 8.6 Hz, 1H), 5.21-5.07 (m, 1H), 4.45-4.27 (m, ,3H), 3.65-3.51 (m, 1H), 3.46- 3.33 (m, 2H), 3.21-3.07 (m, 2H), 2.94-2.86 (s, 2H), 2.81- 2.62 (d, J = 13.2 Hz, 1H), 2.20-1.99 (m, 4H), 1.92- 1.70 (m, 2H), 1.70-1.55 (m, 1H), 1.42-1.28 (d, J = 6.9 Hz, 3H).

1.1 

 36

  Stereoisomer A

2-(2-fluoro-4-((1- (methylsulfonyl) azetidin-3- yl)oxy)benzyl)- (3S)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.50-7.32 (m, 6H), 6.81- 6.70 (m, 2H), 5.10-4.97 (m, 1H), 4.55-4.40 (m, 2H), 4.37-4.23 (m, 3H), 4.18- 4.02 (m, 1H), 3.98-3.85 (m, 2H), 3.10-3.00 (s, 3H), 2.48- 2.30 (m, 1H), 2.16-2.04 (m, 1H), 1.89-1.72 (m, 1H), 1.73-1.60 (m, 1H), 1.13- 1.05 (d, J = 6.8 Hz, 3H).

0.071

 37

  Stereoisomer B

2-(2-fluoro-4-((1- (methylsulfonyl) azetidin-3- yl)oxy)benzyl)- (3S)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.50-7.43 (m, 2H), 7.43- 7.33 (m, 4H), 6.86-6.72 (m, 2H), 5.14-4.99 (m, 1H), 4.48-4.36 (m, 3H), 4.36- 4.26 (m, 2H), 3.97-3.85 (m, 2H), 3.66-3.49 (m, 1H), 3.12-3.02 (s, 3H), 2.81- 2.63 (m, 1H), 2.23-1.98 (m, 2H), 1.70-1.58 (m, 1H), 1.44-1.28 (d, J = 7.0 Hz, 3H).

0.194

 38

  Stereoisomer A

2-(4-((1,1- dioxidotetrahydro- 2H-thiopyran-4- yl)oxy)-2- fluorobenzyl)- (3S)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

0.135

 39

  Stereoisomer B

2-(4-((1,1- dioxidotetrahydro- 2H-thiopyran-4- yl)oxy)-2- fluorobenzyl)- (3S)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.53-7.43 (m, 2H), 7.43- 7.31 (m, 4H), 6.99-6.85 (m, 2H), 4.76-4.67 (m, 1H), 4.53-4.37 (m, 2H), 4.36- 4.25 (m, 1H), 4.19-4.01 (m, 1H), 3.26-3.09 (m, 4H), 2.48-2.36 (m, 1H), 2.29- 2.02 (m, 5H), 1.90-1.70 (m, 1H), 1.70-1.57 (m, 1H), 1.13-1.05 (d, J = 7.0 Hz, 3H).

0.119

 40

  Stereoisomer A

1-(4-(4-(((3S)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.43 (m, 2H), 7.43- 7.32 (m, 3H), 7.29-7.18 (m, 2H), 6.97-6.88 (m, 2H), 4.49-4.40 (d, J = 16.5 Hz, 1H), 4.40-4.29 (m, 1H), 4.24-4.14 (d, J = 16.5 Hz, 1H), 4.13-3.98 (m, 1H), 3.64-3.48 (m, 4H), 3.17- 3.10 (m, 2H), 3.10-3.01 (m, 2H), 2.47-2.30 (m, 1H), 2.15-2.05 (m, 1H), 2.03 (s, 3H), 1.89-1.70 (m, 1H), 1.70-1.52 (m, 1H), 1.17- 1.03 (d, J = 6.9 Hz, 3H).

0.081

 41

  Stereoisomer B

1-(4-(4-(((3S)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.50-7.43 (m, 2H), 7.41- 7.36 (m, 3H), 7.28-7.20 (m, 2H), 7.00-6.95 (m, 2H), 4.39-4.24 (m, 3H), 3.61- 3.55 (m, 4H), 3.21-3.14 (m, 2H), 3.12-3.08 (m, 2H), 2.78-2.63 (m, 1H), 2.12- 1.95 (m, 6H), 1.64-1.53 (m, 1H), 1.37-1.27 (d, J = 7.1 Hz, 3H).

0.126

 42

  Stereoisomer A

1-(4-(5-(((3S)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)pyridin- 2-yl)piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 8.16-8.09 (d, J = 2.3 Hz, 1H), 7.61-7.53 (m, 1H), 7.52-7.43 (m, 2H), 7.43- 7.33 (m, 3H), 6.95-6.83 (d, J = 8.8 Hz, 1H), 4.46-4.14 (m, 3H), 3.65-3.51 (m, 7H), 3.51-3.42 (m, 2H), 2.87- 2.60 (m, 1H), 2.17-1.93 (s, 5H), 1.69-1.53 (m, 1H), 1.42-1.23 (d, ,J = 7.1 Hz, 3H).

0.837

 43

  Stereoisomer B

1-(4-(5-(((3S)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)pyridin- 2-yl)piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 8.16-8.09 (d, J = 2.0 Hz, 1H), 7.59-7.51 (dd, J = 8.6, 2.5 Hz, 1H), 7.51-7.43 (m, 2H), 7.43-7.31 (m, 3H), 6.95-6.78 (d, J = 8.9 Hz, 1H), 4.51-4.30 (m, 2H), 4.30-4.13 (m, 1H), 4.15- 3.92 (m, 1H), 3.63-3.48 (m, 6H), 3.48-3.38 (m, 2H), 2.47-2.26 (m, 1H), 2.16- 2.05 (m, 1H), 2.02 (s, 3H), 1.92-1.70 (m, 1H), 1.70- 1.56 (m, 1H), 1.19-1.07 (d, J = 6.8 Hz, 3H).

1.5 

 44

  Stereoisomer A

(3S)-3-Methyl-2- (4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.52-7.43 (m, 2H), 7.43- 7.32 (m, 3H), 7.32-7.25 (m, 2H), 7.01-6.87 (m, 2H), 4.62-4.49 (m, 1H), 4.49- 4.42 (m, 1H), 4.42-4.34 (dd, J = 12.8, 3.5 Hz, 1H), 4.27-4.18 (d, J = 16.6 Hz, 1H), 4.16-3.92 (m, 1H), 3.43-3.30 (m, 2H), 3.20- 3.02 (m, 2H), 2.93-2.81 (s, 3H), 2.46-2.28 (m, 1H), 2.17-2.04 (m, 1H), 2.04- 1.92 (m, 2H), 1.90-1.56 (m, 4H), 1.14-1.04 (d, J = 6.8 Hz, 3H).

0.014

 45

  Stereoisomer B

(3S)-3-Methyl-2- (4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.50-7.44 (m, 2H), 7.44- 7.33 (m, 3H), 7.33-7.26 (m, 2H), 7.06-6.94 (m, 2H), 4.63-4.49 (m, 1H), 4.45- 4.26 (m, 3H), 3.61-3.45 (m, 1H), 3.44-3.31 (m, 2H), 3.20-3.05 (m, 2H), 2.95- 2.85 (s, 3H), 2.83-2.63 (m, 1H), 2.17-1.93 (m, 4H), 1.85-1.66 (m, 2H), 1.66- 1.52 (m, 1H), 1.38-1.29 (d, J = 7.0 Hz, 3H).

0.022

 46

  Stereoisomer A

1-(4-(4-(((3R)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.50-7.43 (m, 2H), 7.43- 7.31 (m, 3H), 7.28-7.18 (m, 2H), 6.99-6.87 (m, 2H), 4.51-4.40 (d, J = 16.5 Hz, 1H), 4.40-4.30 (m, 1H), 4.27-4.15 (d, J = 16.5 Hz, 1H), 4.15-3.89 (m, 1H), 3.62-3.49 (m, 4H), 3.19- 3.09 (m, 2H), 3.09-3.00 (m, 2H), 2.46-2.32 (m, 1H), 2.13-2.05 (m, 1H), 2.02 (s, 3H), 1.93-1.71 (m, 1H), 1.71-1.57 (m, 1H), 1.14- 1.01 (d, J = 6.9 Hz, 3H).

 47

  Stereoisomer B

1-(4-(4-(((3R)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)ethanone

¹H NMR (400 MHz, DMSO) δ 7.52-7.43 (m, 2H), 7.43- 7.32 (m, 3H), 7.29-7.19 (m, 2H), 7.02-6.91 (m, 2H), 4.44-4.21 (m, 3H), 3.63- 3.54 (m, 4H), 3.54-3.46 (m, 1H), 3.23-3.13 (m, 2H), 3.12-3.05 (m, 2H), 2.82- 2.63 (m, 1H), 2.13-1.95 (m, 5H), 1.66-1.54 (m, 1H), 1.37-1.28 (d, J = 7.1 Hz, 3H).

0.299

 48

  Stereoisomer A

1-{4-[5-((3R)-3- Methyl-1,1-dioxo- 6-phenyl- [1,2]thiazinan-2- ylmethyl)-pyridin- 2-yl]-piperazin-1- yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 8.16-8.08 (d, J = 2.3 Hz, 1H), 7.64-7.53 (m, 1H), 7.52-7.43 (m, 2H), 7.43- 7.33 (m, 3H), 6.93-6.84 (d, J = 8.7 Hz, 1H), 4.46-4.16 (m, 3H), 3.63-3.50 (m, 7H), 3.50-3.43 (m, 2H), 2.81- 2.60 (m, 1H), 2.15-1.98 (m, 5H), 1.70-1.48 (m, 1H), 1.41-1.27 (d, J = 7.0 Hz, 3H).

1.5 

 49

  Stereoisomer B

1-{4-[5-((3R)-3- Methyl-1,1-dioxo- 6-phenyl- [1,2]thiazinan-2- ylmethyl)-pyridin- 2-yl]-piperazin-1- yl}-ethanone

¹H NMR (400 MHz, DMSO) δ 8.16-8.10 (d, J = 2.3 Hz, 1H), 7.61-7.53 (m, 1H), 7.51-7.43 (m, 2H), 7.43- 7.31 (m, 3H), 6.89-6.80 (d, J = 8.8 Hz, 1H), 4.50-4.34 (m, 2H), 4.30-4.14 (m, 1H), 4.12-3.95 (m, 1H), 3.58- 3.48 (s, 6H), 3.48-3.39 (m, 2H), 2.46-2.27 (m, 1H), 2.15-2.06 (m, 1H), 2.03 (s, 3H), 1.91-1.71 (m, 1H), 1.70-1.51 (m, 1H), 1.17- 1.08 (d, J = 6.6 Hz, 3H).

5.5 

 50

  Stereoisomer A

2-[6-(1- Methanesulfonyl- piperidin-4-yloxy)- pyridin-3- ylmethyl]-(3R)-3- methyl-6-phenyl- [1,2]thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 8.18-8.13 (d, J = 2.4 Hz, 1H), 7.77-7.67 (m, 1H), 7.50-7.44 (m, 2H), 7.44- 7.26 (m, 3H), 6.89-6.80 (d, J = 8.7 Hz, 1H), 5.23-5.10 (m, 1H), 4.48-4.27 (m, 3H), 3.65-3.50 (m, 1H), 3.49- 3.32 (m, 2H), 3.22-3.06 (m, 2H), 2.96-2.84 (s, 2H), 2.83- 2.61 (m, 1H), 2.17-1.96 (m, 4H), 1.90-1.68 (m, 2H), 1.68-1.57 (m, 1H), 1.42- 1.31 (d, J = 7.1 Hz, 3H).

0.168

 51

  Stereoisomer B

2-[6-(1- Methanesulfonyl- piperidin-4-yloxy)- pyridin-3- ylmethyl]-(3R)-3- methyl-6-phenyl- [1,2]thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 8.18-8.10 (d, J = 2.0 Hz, 1H), 7.78-7.67 (m, 1H), 7.49-7.43 (m, 2H), 7.43- 7.32 (m, 3H), 6.89-6.74 (d, J = 8.3 Hz, 1H), 5.21-5.03 (m, 1H), 4.53-4.36 (m, 2H), 4.36-4.20 (m, 1H), 4.19- 3.94 (m, 1H), 3.44-3.33 (m, 2H), 3.20-3.06 (m, 2H), 2.89 (s, 2H), 2.47-2.29 (m, 1H), 2.20-1.97 (m, 3H), 1.94-1.58 (m, 4H), 1.17- 1.06 (d, J = 6.8 Hz, 3H).

1.4 

 52

(3R)-3-Methyl-2- (4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.52-7.43 (m, 2H), 7.43- 7.34 (m, 3H), 7.34-7.24 (m, 2H), 7.06-6.94 (m, 2H), 4.65-4.47 (m, 1H), 4.46- 4.24 (m, 3H), 3.66-3.44 (m, 1H), 3.44-3.31 (m, 2H), 3.22-3.05 (m, 2H), 2.94- 2.84 (s, 3H), 2.80-2.62 (m, 1H), 2.15-1.90 (m, 4H), 1.83-1.65 (m, 2H), 1.65- 1.51 (m, 1H), 1.42-1.27 (d, J = 7.1 Hz, 3H).

0.020

 53

2-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)- (3R)-3-methyl-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.51-7.43 (m, 2H), 7.43- 7.30 (m, 4H), 6.96-6.89 (m, 1H), 6.89-6.83 (m, 1H), 4.71-4.52 (m, 1H), 4.50- 4.32 (m, 3H), 3.68-3.46 (m, 1H), 3.44-3.31 (m, 2H), 3.22-3.04 (m, 2H), 2.95- 2.86 (s, 2H), 2.83-2.60 (m, 1H), 2.24-1.92 (m, 4H), 1.92-1.67 (m, 2H), 1.67- 1.57 (m, 1H), 1.44-1.28 (d, J = 6.9 Hz, 3H).

0.006

 54

  Stereoisomer A

2-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1- dioxide

0.037

 55

  Stereoisomer B

2-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-6- phenyl-1,2- thiazinane 1,1- dioxide

¹H NMR (400 MHz, DMSO) δ 7.48-7.30 (m, 6H), 6.97- 6.89 (m, 1H), 6.89-6.84 (m, 1H), 4.68-4.56 (m, 1H), 4.56-4.47 (m, 1H), 4.47- 4.38 (m, 1H), 4.38-4.30 (m, 1H), 3.57-3.41 (m, 1H), 3.42-3.31 (m, 2H), 3.19- 3.05 (m, 3H), 2.94-2.88 (s, 3H), 2.48-2.39 (m, 1H), 2.21-2.08 (m, 1H), 2.08- 1.91 (m, 3H), 1.82-1.68 (m, 2H), 1.68-1.57 (m, 1H).

0.086

 56

  Stereoisomer A

5-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-3- phenyl-1,4,5- oxathiazepane 4,4- dioxide

¹H NMR (400 MHz, DMSO) δ 7.48-7.30 (m, 6H), 6.97- 6.89 (m, 1H), 6.89-6.84 (m, 1H), 4.68-4.56 (m, 1H), 4.56-4.47 (m, 1H), 4.47- 4.38 (m, 1H), 4.38-4.30 (m, 1H), 3.57-3.41 (m, 1H), 3.42-3.31 (m, 2H), 3.19- 3.05 (m, 3H), 2.94-2.88 (s, 3H), 2.48-2.39 (m, 1H), 2.21-2.08 (m, 1H), 2.08- 1.91 (m, 3H), 1.82-1.68 (m, 2H), 1.68-1.57 (m, 1H).

0.094

 57

  Stereoisomer B

5-(2-fluoro-4-((1- (methylsulfonyl) piperidin-4- yl)oxy)benzyl)-3- phenyl-1,4,5- oxathiazepane 4,4- dioxide

0.014

 58

  Stereoisomer A

Cyclopropyl(4-(3- fluoro-4-(((3S)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)methanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.43 (m, 2H), 7.43- 7.33 (m, 3H), 7.33-7.25 (m, 1H), 6.87-6.75 (m, 2H), 4.43-4.34 (m, 3H), 3.90- 3.70 (s, 2H), 3.69-3.49 (m, 3H), 3.26-3.08 (s, 4H), 2.77- 2.59 (d, J = 13.2 Hz, 1H), 2.17-1.93 (m, 3H), 1.67- 1.57 (d, J = 37.7 Hz, 1H), 1.40-1.31 (d, J = 7.1 Hz, 3H), 0.81-0.68 (m, 4H).

0.014

 59

  Stereoisomer B

Cyclopropyl(4-(3- fluoro-4-(((3S)-3- methyl-1,1- dioxido-6-phenyl- 1,2-thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)methanone

¹H NMR (400 MHz, DMSO) δ 7.50-7.43 (m, 2H), 7.43- 7.29 (m, 4H), 6.85-6.78 (m, 1H), 6.78-6.69 (m, 1H), 4.50-4.36 (m, 2H), 4.35- 4.22 (m, 1H), 4.20-3.99 (m, 1H), 3.89-3.74 (m, 2H), 3.69-3.52 (m, 2H), 3.25- 3.08 (d, J = 26.2 Hz, 4H), 2.46-2.38 (m, 1H), 2.18- 1.94 (m, 2H), 1.89-1.72 (m, 1H), 1.72-1.59 (m, 1H), 1.16-1.04 (d, J = 6.8 Hz, 3H), 0.85-0.65 (m, 4H).

0.015

 60

  Stereoisomer A

Cyclopropyl(4-(4- (((3S)-3-methyl- 1,1-dioxido-6- phenyl-1,2- thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)methanone

¹H NMR (400 MHz, DMSO) δ 7.49-7.43 (m, 2H), 7.43- 7.34 (m, 3H), 7.29-7.22 (m, 2H), 6.97-6.90 (m, 2H), 4.52-4.40 (d, J = 16.4 Hz, 1H), 4.40-4.31 (dd, J = 12.9, 3.5 Hz, 1H), 4.25- 4.15 (d, J = 16.5 Hz, 1H), 4.11-4.00 (m, 1H), 3.89- 3.72 (m, 2H), 3.70-3.52 (m, 3H), 3.21-3.04 (m, 5H), 2.46-2.39 (m, 2H), 2.17- 1.95 (m, 2H), 1.88-1.73 (m, 1H), 1.70-1.56 (m, 1H), 1.15-1.05 (d, J = 6.9 Hz, 3H), 0.81-0.66 (m, 4H).

0.015

 61

  Stereoisomer B

Cyclopropyl(4-(4- (((3S)-3-methyl- 1,1-dioxido-6- phenyl-1,2- thiazinan-2- yl)methyl)phenyl) piperazin-1- yl)methanone

¹H NMR (400 MHz, DMSO) δ 7.50-7.44 (m, 2H), 7.43- 7.36 (m, 3H), 7.28-7.22 (m, 2H), 7.02-6.95 (m, 2H), 4.40-4.22 (m, 3H), 3.87- 3.77 (m, 2H), 3.68-3.57 (m, 2H), 3.55-3.49 (m, 1H), 3.23-3.08 (m, 4H), 2.75- 2.68 (m, 1H), 2.11-1.97 (m, 3H), 1.64-1.56 (m, 1H), 1.36-1.29 (d, J = 7.1 Hz, 3H), 0.79-0.68 (m, 4H).

0.061