Azo dyes from five membered ring heterocyclic amines and aniline, tetrahydroquinoline and benzomorpholine couplers containing thiosulfate alkyl groups
专利汇可以提供Azo dyes from five membered ring heterocyclic amines and aniline, tetrahydroquinoline and benzomorpholine couplers containing thiosulfate alkyl groups专利检索，专利查询，专利分析的服务。并且Disclosed are mono azo dyes derived from diazotized 5-membered heterocyclic amines and certain aniline, 1,2,3,4-tetrahydroquinoline, and benzomorpholine couplers containing thiosulfate alkyl groups. These dyes are useful for dyeing synthetic fibers, cellulose acetate and wool, and particularly impart fast violet to blue shades on polyamide fibers, and in general, exhibit improved properties such as fastness to light, sublimation, ozone, oxides of nitrogen, perspiration, crock, and wash, and exhibit excellent build, pH stability, bloom resistance, depth of shade, leveling, migration, and the like. The dyes have the general formula:D--N.dbd.N--Couplerwherein D is a thiadiazol, isothiazol, pyrazol or thiophene type radical, and the Coupler is an aniline, tetrahydroquinoline, or benzomorpholine derivative wherein a --ZSSO.sub.3 M group is attached to the nitrogen thereof, the coupler ring may contain substituents such as alkyl, alkoxy, halogen, acylamido, alkylthio or aryloxy, the remaining hydrogen of the aniline coupler may be replaced by a substituent such as alkyl, substituted alkyl, alkenyl, aryl, or cycloalkyl, M is Na.sup.+, K.sup.+, NH.sub.4.sup.+ or H.sup.+, and Z is a linking group such as ethylene.，下面是Azo dyes from five membered ring heterocyclic amines and aniline, tetrahydroquinoline and benzomorpholine couplers containing thiosulfate alkyl groups专利的具体信息内容。
We claim:1. A compound of the formulae D-N.dbd.N-Coupler, wherein D is selected from the heterocyclic amines of the formulae ##STR68## wherein ring A is unsubstituted or substituted with a group selected from alkyl, alkoxy, halogen, alkylsulfonyl, SO.sub.2 -aryl, SO.sub.2 NH.sub.2, SO.sub.2 NH-alkyl, SO.sub.2 N-(dialkyl), alkanoylamino, aryl, arylthio, alkenylthio, cyclohexylthio, thiocyano, cyclohexylsulfonyl, alkylthio, and cyclohexyl;ring B is unsubstituted or substituted with a group selected from alkyl, aryl, alkylthio, cyclohexylthio and alkylsulfonyl;ring C is unsubstituted or substituted with one or two groups selected from alkyl, halogen, cyano, carbamoyl, CONH-alkyl, alkoxycarbonyl, alkylthio, alkenylthio, arylthio, cyclohexylthio, aryloxy, and alkoxy;ring D is unsubstituted or substituted with one or two groups selected from alkyl, alkoxycarbonyl, alkylthio, aryl, cyano, carbamoyl, alkyl carbamoyl, alkylcarbonyl and alkyl sulfonyl; and the A group on the 1-nitrogen of ring D is hydrogen, alkyl, alkoxycarbonyl, aryl, alkylsulfonyl, arylsulfonyl, or alkanoyl;ring E is unsubstituted or substituted with one to three groups selected from alkyl, cyano, alkoxycarbonyl, alkanoyl, aroyl, alkylsulfonyl, arylsulfonyl, carbamoyl, alkyl carbamoyl, aryl, halogen, sulfamoyl, and formyl;wherein the various alkyl or alkylene portions of the above groups are unsubstituted or substituted with one to three groups selected from hydroxy, halogen, alkoxy, aryl, aryloxy, cyclohexyl, alkylcyclohexyl, acyloxy, alkoxy carbonyl, acylamido, alkylsulfonamido, succinimido, glutarimido, phthalimido, 2-pyrrolidono, cyano, carbamoyl, alkoxyalkoxy, alkylthio, halogen, arylthio, alkylsulfonyl and arylsulfonyl;and wherein the various above aryl groups are unsubstituted or substituted with one to three groups selected from alkyl, alkoxy, halogen, alkoxy carbonyl, alkyl sulfonyl, and alkylthio; andthe Coupler is selected from those of the formulae ##STR69## wherein R.sub.1 is selected from hydrogen; alkyl; halogen; alkoxy; aryloxy; --NHCO--R.sub.5 ; --NHSO.sub.2 --R.sub.5 ; wherein R.sub.5 is selected from alkyl and alkyl substituted with hydroxy, alkoxy, cyano, aryloxy, aryl, halogen, cycloalkyl, alkyl carbonyloxy, or carbamoyl; aryl; alkylamine; and 2-furyl; R.sub.2 is selected from hydrogen; aryl; cycloalkyl; alkyl and alkyl substituted with alkoxy, alkoxyalkoxy, hydrogen, aryloxy, aryl, cycloalkyl, alkylcycloalkyl, furyl, NHCOR.sub.5, NHSO.sub.2 R.sub.5, aryloxy, carbamoyl, alkyl carbamoyl, cyano, alkanoyloxy, halogen, alkoxycarbonyl, succinimido, glutarimido, phthalimido, 2-pyrrolidono, sulfamoyl, alkyl substituted sulfamoyl, alkylsulfonamido, NHSO.sub.2 -aryl, NHCOO-alkyl, NHCONH-alkyl, formamido, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio, or SO.sub.3 M; n is 0, 1 or 2; M is Na.sup.+, K.sup.+, NH.sub.4.sup.+, or H.sup.+ ; R.sub.3 and R.sub.4 are each selected from hydrogen or alkyl; Z is selected from straight or branched chain alkylene; alkylene substituted with aryl, aryloxy, alkoxy, halogen, aryloxy or SO.sub.3 M; --CH.sub.2 (CH.sub.2).sub.m --X--CH.sub.2 (CH.sub.2).sub.p, where m is 1, 2, or 3, p is 0, 1, 2, or 3, and X is O, S, SO.sub.2, --SO.sub.2 NH--, ##STR70## and the various aryl groups on the couplers are unsubstituted or substituted with alkyl, alkoxy, or halogen.2. A compound according to claim 1 wherein R.sub.1 is selected from hydrogen, alkyl, and alkoxy; R.sub.2 is selected from hydrogen and alkyl; and Z is straight or branched chain alkylene.3. A compound according to claim 1 having the formula ##STR71##4. A compound according to claim 1 having the formula ##STR72##5. A compound according to claim 1 having the formula ##STR73##6. A compound according to claim 1 having the formula ##STR74##7. A compound according to claim 1 having the formula ##STR75##8. A compound according to claim 1 having the formula ##STR76##9. A compound according to claim 1 having the formula ##STR77##10. A compound according to claim 1 having the formula ##STR78##11. A compound according to claim 1 having the formula ##STR79##
This invention concerns mono azo dyes derived from diazotized 5-membered heterocyclic amines and certain aniline, 1,2,3,4-tetrahydroquinoline, and benzomorpholine couplers containing thiosulfate alkyl groups. These dyes are useful for dyeing synthetic fibers, cellulose acetate and wool, and particularly impart fast violet to blue shades on polyamide fibers. The dyes, in general, exhibit improved properties such as fastness to light, sublimation, ozone, oxides of nitrogen, perspiration, crock, and wash, and exhibit excellent build, pH stability, bloom resistance, depth of shade, leveling, migration, and the like.
The dyes of this invention have the general formula:
D--N═N--Coupler
wherein D is a thiadiazol, isothiazol, pyrazol or thiophene type radical, and the Coupler is an aniline, tetrahydroquinoline, or benzomorpholine derivative wherein a --ZSSO3 M group is attached to the nitrogen thereof, the coupler ring may contain substituents such as alkyl, alkoxy, halogen, acylamido, alkylthio or aryloxy, the remaining hydrogen of the aniline coupler may be replaced by a substituent such as alkyl, substituted alkyl, alkenyl, aryl, or cycloalkyl, M is Na+, K+, NH4 + or H+, and Z is a linking group such as ethylene.
More specifically, the Coupler is of the formulae ##STR1## wherein R1 is selected from hydrogen; alkyl; halogen; alkoxy; aryloxy; --NHCO--R5 ; --NHSO2 --R5 ; wherein R5 is selected from alkyl which may be substituted with hydroxy, alkoxy, cyano, aryloxy, aryl, halogen, cycloalkyl, alkylcarbonyloxy, or carbamoyl; aryl; alkylamino; and 2-furyl; R2 is selected from hydrogen; aryl; cycloalkyl; and alkyl which may be substituted with alkoxy, alkoxyalkoxy, hydrogen, aryloxy, aryl, cycloalkyl, alkylcycloalkyl, furyl, acylamido, aryloxy, carbamoyl, alkoxycarbamoyl, alkyl substituted carbamoyl, cyano, alkanoyloxy, halogen, alkoxycarbonyl, succinimido, glutarimido, phthalimido, 2-pyrrolidono, sulfamoyl, alkyl substituted sulfamoyl, alkylsulfonamido, NHSO2 -aryl, NHCOO-alkyl, NHCONH-alkyl, formamido, alkylsulfonyl, arylsulfonyl, alkylthio, arylthio or SO3 M; n is 0, 1 or 2; M is Na+, K+, NH4 +, or H+ ; R3 and R4 are each selected from hydrogen or alkyl; Z is selected from straight or branched chain alkylene; alkylene substituted with aryl, aryloxy, alkoxy, halogen, aryloxy or SO3 M; --CH2 (CH2)m --X--CH2 (CH2)p, where m is 1, 2, or 3, p is 0, 1, 2 or 3, and X is O, S, SO2, --SO2 NH--, ##STR2## the various aryl groups above may be substituted with alkyl, alkoxy, or halogen; and each of the above alkyl, alkylene, alkoxy, alkenyl and the like moieties contain from 1-6 carbons.
The heterocycle D is of the formulae ##STR3## wherein
ring A may bear a substituent selected from alkyl, substituted alkyl, alkoxy, halogen, alkylsulfonyl, SO2 -aryl, SO2 NH2, SO2 NH-alkyl, SO2 N-(di-alkyl), substituted SO2 NH-alkyl, acylamido, aryl, arylthio, alkenylthio, cyclohexylthio, thiocyano, cyclohexylsulfonyl, alkylthio, substituted alkylthio and cyclohexyl;
ring B may bear a substituent selected from alkyl, substituted alkyl, aryl, alkylthio, cyclohexylthio, substituted alkylthio and alkylsulfonyl;
ring B may bear a substituent selected from alkyl, substituted alkyl, aryl, alkylthio, cyclohexylthio, substituted alkylthio and alkylsulfonyl;
ring C may bear one or two substituents selected from alkyl, substituted alkyl, halogen, cyano, carbamoyl, CONH-alkyl, substituted CONH-alkyl, alkoxycarbonyl, alkylthio, substituted alkylthio, alkenylthio, arylthio, cyclohexylthio, S-heterocycle, aryloxy, and alkoxy;
ring D may bear one or two substituents selected from alkyl, substituted alkyl, alkoxycarbonyl, alkylthio, aryl, cyano, carbamoyl, alkyl carbamoyl, alkylcarbonyl, substituted alkyl carbamoyl, and alkyl sulfonyl; and the A group on the 1-nitrogen of ring D may be hydrogen, alkyl, alkoxycarbonyl, aryl, alkylsulfonyl, arylsulfonyl, or alkanoyl;
ring E may be substituted with one to three substituents selected from alkyl, substituted alkyl, cyano, alkoxycarbonyl, acyl, aroyl, alkylsulfonyl, arylsulfonyl, carbamoyl, alkyl carbamoyl, substituted alkyl carbamoyl, aryl, halogen, sulfamoyl, substituted alkyl, and formyl;
wherein the various alkyl, alkylene, alkoxy and other such moieties contain from 1-6 carbons and may bear one to three substituents selected from hydroxy, halogen, alkoxy, aryl, aryloxy, cyclohexyl, alkylcyclohexyl, acyloxy, alkoxy carbonyl, acylamido, alkylsulfonamido, succinimido, glutarimido, phthalimido, 2-pyrrolidono, cyano, carbamoyl, alkoxy-alkoxy, alkylthio, halogen, arylthio, alkylsulfonyl and arylsulfonyl;
and wherein the various aryl groups may be substituted with one to three substituents selected from alkyl, alkoxy, halogen, alkoxy carbonyl, alkyl sulfonyl, and alkylthio.
The following couplers are particularly valuable in the practice of this invention. ##STR4## The couplers of this invention are prepared by reacting N-chloro (or bromo) alkyl aromatic amines with an alkali thiosulfate salt.
The following coupler intermediates are typical of those appropriate for reacting with sodium thiosulfate. ##STR5##
The halogen containing couplers are in general prepared by reacting the corresponding known hydroxy compounds with POCl3, SOCl2, POBr3, PBr3, and the like by methods well known in the art. The tetrahydroquinoline and benzomorpholine intermediates are similarly prepared.
This invention will be further illustrated by the following examples although it will be understood that these examples are included merely for purposes of illustration and are not intended to limit the scope of the invention.
Preparation of Typical Couplers
EXAMPLE 1
Sodium S-2-[ethyl(3-methylphenyl)amino] ethyl thiosulfate
Sodium thiosulfate (49.6 g, 0.2 m), sodium iodide (1 g), N-2-chloroethyl-N-ethyl-m-toluidine (19.8 g, 0.1 m), and 200 ml water were mixed and heated at about 95° C. for about 11/2 hrs. The reaction mixture was cooled to about 20° C. and filtered. The white solid was washed with hexane and dried in air. Yield--26.0 g (87.5%).
EXAMPLE 2
Sodium S-2-(1,2,3,4-tetrahydro-2,2,4,7-tetramethyl-1-quinolinyl)ethyl thiosulfate
A mixture of sodium thiosulfate (49.6 g, 0.2 m), sodium iodide (1 g), N-(2-chloroethyl)-2,2,4,7-tetramethyl-1,2,3,4-tetrahydroquinoline (25.2 g, 0.1 m), water (100 ml), and ethanol (100 ml) was refluxed fro 3 hrs. The mixture was cooled and extracted with 2-75 ml portions of toluene. The aqueous layer then contained essentially pure product and aliquots were used to prepare dyes without further purification.
EXAMPLE 3
Sodium S-2(3,4-dihydro-3,6-dimethyl-2H-1,4-benzoxazin-4-yl)ethyl thiosulfate
Sodium thiosulfate (0.2 m), sodium iodide (1 g), N-(2-chloroethyl)-3,6-dimethyl-2H-1,4-benzoxazine, water (150 ml), and ethanol (75 ml) were mixed and heated at reflux for 3 hrs. The alcohol was distilled off and the reaction mixture was cooled. The product, a white solid, was collected by filtration and dried in air. The yield was essentially quantitative. Preparation of the Dyes
EXAMPLES 4-8
Diazotization and Coupling of 2-Amino-5-ethylthio-1,3,4-thiadiazole
Sodium nitrite (3.6 g.) is added portionwise to 25 ml of concentrated H2 SO4. The solution is cooled and 100 ml of 1:5 acid (1 part propionic :1 part acetic) is added below 15° C. The mixture is cooled and 8.05 g. (0.05 m) of 2-amino-5-ethylthio-1,3,4-thiadiazole is added below 10° C. After stirring at 0°-5° C. for 2 hrs., a 0.005 m aliquot of the diazonium salts is added to 0.005 m of the following couplers in water or dilute sulfuric acid, keeping the temperature below 5° C.
EXAMPLE 4
Sodium S-2[ethyl(3-methylphenyl)amino]ethyl thiosulfate
EXAMPLE 5
Sodium S-2[ethyl(phenyl)amino]ethyl thiosulfate
EXAMPLE 6
Sodium S-2-(1,2,3,4-tetrahydro-2,2,4,7-tetramethyl-1-quinolinyl)ethyl thiosulfate
EXAMPLE 7
Sodium S-2-(2,7-dimethyl-1,2,3,4-tetrahydro-1-quinolin yl)ethyl thiosulfate
EXAMPLE 8
Sodium S-2-(3,4-dihydro-3,6-dimethyl-2H-1,4-benzoxazin-4-yl)ethyl thiosulfate
The mineral acid is neutralized with sodium acetate and the coupling mixture allowed to stand for 1 hr. Water is added to make a total volume of 200-300 ml. and the dyes are collected by filtration, washed with water, and dried in air.
The dyes usually contain about an equal weight of dye and sodium sulfate as they are isolated and are used for dying polyamide fibers red shades without further purification.
EXAMPLES 9-13
Diazotization of 5-Amino-3-ethylthio-1,2,4-thiadiazole
5-Amino-3-ethylthio-1,2,4-thiadiazole (8.05 g., 0.05 m) is diazotized exactly as described in Examples 4-8 and a 0.005 m aliquot coupled to 0.005 m portion of the couplers of Examples 4-8 in the manner previously illustrated.
EXAMPLES 14-18
Diazotization of 5-Amino-3-methyl-4-cyano isothiazole
To 25 ml of concentrated H2 SO4 is added 3.6 g. of NaNO2 allowing the temperature to rise. The solution is cooled and 50 ml of 1:5 acid is added below 10° C. Stirring is continued and 6.95 g. (0.05 m) of 5-amino-3-methyl-4-cyanoisothiazole is added below 5° C., followed by an additional 50 ml of 1:5 acid. After stirring at 0°-5° C. for 2 hrs., a 0.005 m aliquot of the diazoniu m salt is coupled to 0.005 m of the couplers of Examples 4-8 as previously described to produce rubine to violet dyes for polyamides.
EXAMPLES 19-23
Diazotization of 5-Amino-4-carbomethoxypyrazole
Nitrosyl sulfuric acid is prepared by adding 3.6 g. NaNO2 to 25 ml of concentrated H2 SO4. The solution is cooled and 100 ml of 1;5 acid is below 20° C. After further cooling, 5-amino-4-carbomethoxypyrazole (7.05 g., 0.05 m) is added at 0°-5° C. and stirring continued for 2 hrs. A 0.005 m aliquot of the diazonium solution is coupled to 0.005 m. of the couplers of Examples 4-8 in the manner previously described to produce red dyes for polyamides.
EXAMPLES 24-28
Diazotization of 2-Amino-3-carbomethoxy-5-isobutyrylthiophene
To 150 g. of 60% aqueous acetic acid is added 11.35 g. (0.05 m) of 2-amino-3-carbomethoxy-5-isobutyrylthiophene at room temperature. Ten grams of concentrated H2 SO4 is added and the mixture cooled to 0° C. A solution of 3.6 g NaNO2 in 25 ml of conc. H2 SO4 is added below 10° C. and stirring continued for 1 hr. at 0°-5° C. A 0.005 m aliquot of this diazonium salt is coupled to 0.005 m portions of the couplers of Examples 4-8 as previously illustrated to produce violet to reddish-blue dyes for polyamides.
The following tables of dyes will further illustrate the invention.
TABLE 1__________________________________________________________________________ ##STR6##R (R1)m R2 Z M__________________________________________________________________________5-CH3 2-CH3 H CH2 CH2 K+5-CH2 CH3 2-Cl " " "5-CH2 CH(CH3) 2,5-di-Cl " " "5-C6 H5 2,5-di-CH3 " " "5-C6 H11 2,5-di-OCH3 " " "5-C6 H4p-Cl 3-OCH3 C2 H5 " "5-C6 H4o-CH 3 2-OCH3, 5-NHCOCH3 H " "5-C6 H4m-OCH 3 2-CH3, 3-Cl " " "5-SCH3 2-OCH3 , 5-Cl " " "" 3-NHCOCH3 C2 H5 " "" 3-NHCOC2 H5 C2 H4 OCH3 " "" 3-NHCOCH2 OH CH2 C6 H5 " "" 3-NHCOCH2 OCH3 C6 H11 " "H 3-NHCOC6 H5 CH2 C6 H11 " "" 3-NHCOOC2 H5 CH2 CH2 OC6 H5 " "" 3-NHCONHC2 H5 CH2 CH2 OH " "5-OC2 H5 3-NHCOC6 H11 CH2 CH(CH3)2 " "5-SC2 H5 3-NHCOCH2 CN CH2 CH2 CH2 CH3 " "" 3-NHCOCH2 OC6 H5 CH2 CH2 OCOCH3 " "" 3-NHCOCH2 C6 H5 CH2 CH2 CONH2 " "" 3-CH.sub. 3 CH2 CH2 NHCOCH3 " "" " CH2 CH2 NHSO2 CH3 " "" " CH2 CH2 SO2 NH2 " "" " CH2 CH2 CH2 SO2 CH3 " "5-Cl " CH2 CH2 SCH3 " "5-SO2 CH3 H ##STR7## CH2 CH2 CH2 Na+5-OC4 H9n " ##STR8## " "5-SCH2 CH2 OH 3-OC6 H5 ##STR9## " NH4 + 45-SCH2 CH2 COOCH3 3-CH3 C6 H5 CH2 CH2 Na+ ##STR10## " ##STR11## CH2 CH(CH2 OC6 H5) "5-SCH2 SC6 H5 " CH2 CH2 COOCH3 CH2 CH(C6 H5) "5-SO2 CH3 " CH2 CH2 CN CH2 CH(CH3) "5-SO2 NH2 " C2 H5 CH2 CH(OH)CH2 "5-SO2 NHC2 H5 2-CH3 S H CH2 CH2 CH2 CH2 "5-SCN 3-CH3 C2 H4 OC2 H4 OC2 H5 CH2 CH(OCOCH3)CH2 "5-SO2 N(CH3)2 " CH2 CH(OH)CH2 Cl CH2 CH.sub. 2 "5-SO3 C6 H5 2-OCH3, 5-CH3 C2 H5 " "5-SCH2 CHCH2 " H CH2 CH2 OCH2 CH2 "5-SCH2 CH2 OCH3 " H " " ##STR12## " " CH2 CH2 SO2 CH2 CH2 K+5-SC6 H11 3-CH3 C2 H5 CH2 CH2 SCH2 CH2 "5-SC6 H5 " " CH2 CH2 N(SO2 CH3)CH2 CH2 "5-SO2 C6 H5 " " CH2 CH2 NHSO2 CH2 CH2 CH2 CH2 "5-I " " CH2 CH2 SO2 NHCH2 CH2 "5-Br " " CH2 CH2 N(COCH3)CH. sub.2 CH2 " ##STR13## " " CH2 CH2 CONHC2 H4 "5-SCH2 CH2 NHSO2 CH3 " " CH2 CH2 NHCOCH2 "5-SCH2 CH2 NHCOCH3 " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 "5-SCH2 CH2 OC6 H5 " " CH2 CH2 SO2 N(CH3)CH2 CH2 "5-SCH2 CH2 C6 H5 " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "5-SCH2 CH2 OC2 H5 " " CH2 CH2 N(SO2 C6 H11)CH2 "H25-SO2 C6 H11 " " CH2 CH2 N(COCH3)CH. sub.2 CH.sub. 2 "5-CH3 " " CH2 CH(CH2 OCH3) "" " " CH2 CH(Cl)CH2 "" " " CH2 CH2 NHCONHC2 H4 "5-NHCOCH3 " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "__________________________________________________________________________
TABLE 2__________________________________________________________________________ ##STR14##R (R1)m R3 R4 Z M__________________________________________________________________________H H CH3 CH3 CH2 CH2 K+" 7-CH3 " " " "" 7-OCH3 " " " "5-CH3 7-Cl " " " "5-CH2 CH3 5-CH3, 8-OCH3 " " " "5-CH(CH3)2 5,8-di-OCH3 " " " "5-CH2 CH(CH3)2 5,8-di-CH3 " " " "5-C6 H5 5-Cl, 8-OCH3 " " " "5-C6 H11 8-OCH3 " " " "5-C6 H4o-Cl 8-OC2 H5 H H " "5-C6 H4n-CH 3 7-CH3 " " " "5-C6 H4p-OCH 3 7-NHCOCH3 CH3 CH3 " Na+5-OC2 H5 7-NHCOH " " " "" 7-NHCOCH2 OCH3 " " " "" 7-NHCOCH2 OC6 H5 H CH(CH3)2 " "" 7-NHCOCH2 C6 H5 " " " "" 7-NHCOCH2 Cl " " " "" 7-NHCOC6 H5 " " " "" 7-NHCOC6 H11 CH3 CH3 " "5-Cl 7-NHCONHC2 H5 " " " "" 7-NHSO.sub. 2 CH3 " " " "" 7-NHCOCH2 CN " " " "" 7-NHCOCH2 OH " " " "5-I 7-NHCOOC2 H5 " " CH2 CH2 CH2 "5-Br ##STR15## " " " "5-SO2 CH3 8-OC4 H9n H CH3 CH2 CH2 "5-SO2 NH2 7-CH3 CH3 H " "5-SO2 N(CH3)2 ##STR16## " CH3 " "5-SO2 N(C2 H5)2 7-OC2 H5 " " " "8-SO2 NHC3 H6 OCH3 7-OC4 H9n " " " "5-SO2 CH2 CH2 OC2 H5 7-CH3 " H " "5-SC6 H5 " " " " "5-SC6 H11 " " " CH2 CH2 CH2 CH2 "5-SO2 C6 H5 " " " CH2 CH2 "5-SO3 C6 H5 " " " " "5-SCH2 CH2 OH " " " " "5-SCH2 CHCH3 " " " CH2 CH2 SO2 CH2 CH2 K+5-SCH2 COOC2 H5 " " " CH2 CH2 OCH2 CH2 "5-SCH2 C6 H5 " " " CH2 CH2 SCH2 CH2 "5-SCH2 C6 H11 " " " CH2 CH(C6 H5) "5-SCH2 CH2 OC2 H5 " " " CH.sub. 2 CH(CH3) "5-SCN " " " CH2 CH(OH)CH2 "5-SCH2 CH2 NHCOCH3 " " " CH2 CH(Cl)CH2 " ##STR17## " " " CH2 CH(CH2 OCH2 CH3) "5-SCH2 CH2 OC6 H5 " " " CH2 CH(CH2 OC6 H5) "5-SCH2 CH3 " " " CH2 CH2 N(SO2 CH3)CH2 CH2 "" " " " CH2 CH2 CH2 NHSO2 CH2 CH2 "" " " " CH2 CH2 SO2 NHCH2 CH2 "" " " " CH2 CH2 NHCOCH2 "" " " " CH2 CH2 NHCOOCH2 CH2 "" " " " CH2 CH2 COOCH2 CH2 "" " " " CH2 CH2 CONHC2 H4 "5-SCH3 " " " CH2 CH2 NHCONHC2 H4 "" " " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 "" " " " CH2 CH2 N(COCH3)CH. sub.2 CH2 "" " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "5-NHCOCH3 " " " CH2 CH2 SO2 N(CH3)CH2 CH2 "__________________________________________________________________________
TABLE 3__________________________________________________________________________ ##STR18##R (R1)m R3 Z M__________________________________________________________________________H 6-CH3 H CH2 CH2 K+" H H " "" " CH3 " "5-CH3 6-CH3 " " "5-CH(CH3)2 " " CH2 CH2 CH2 CH2 "5-CH2 CH(CH3)2 6-OCH3 " " "5-C6 H5 " " CH2 CH2 "5-C6 H4p-Cl 6-CH3 " CH2 CH2 OCH2 CH2 "5-C6 H4p-OCH 3 " " CH2 CH2 SO2 CH2 "H25-C6 H4n-CH 3 " " CH2 CH2 SCH2 CH2 "5-OC2 H5 " " CH2 CH(CH3) "5-OCH(CH3)2 " " CH2 CH(C6 H5) "5-C6 H11 6-OC2 H5 " CH2 CH2 "5-SCN 6-NHCOCH3 " " Na+5-SCH3 6-NHCOH " " "5-SCH2 CH(CH3)2 6-NHCOCH2 CH2 OCH3 " " "5-SCH2 CHCH2 6-NHCOCH2 Cl " " "5-SC6 H11 6-NHCOCH2 CN " " "5-SC6 H5 6-NHCOCH2 CONH2 " " "5-SCH2 C6 H5 6-NHCOCH2 OC6 H5 " " "5-SCH2 CH2 OC6 H5 6-NHCOOC2 H5 " " "5-SCH2 CH2 OC2 H5 6-NHCONHC2 H5 " " "5-SCH2 CH2 OH 6-NHCOC6 H5 " " "5-SCH2 CH2 Cl 6-NHCOC6 H11 " " "5-SCH2 COOC2 H5 6-NHSO2 CH3 " " "5-SCH2 CH2 OCOCH3 6-NHCOCH2 CH2 OCOCH3 " " "5-SCH2 C6 H11 ##STR19## " " "5-SO2 CH3 6-NHCOCH2 CH2 CH2 OH " " "5-SO2 C4 H9n 6-CH3 " CH2 CH2 CH2 "5-SO2 CH2 CH2 OCH3 " " CH2 CH2 "5-SO2 C6 H5 " " " "5-SO2 C6 H11 " " " "5-SO2 CH2 C6 H5 " " " "5-SO2 CH2 CH2 OH " " " " ##STR20## " " " "5-SCH2 CH2 NHCOCH3 " " " " ##STR21## " H CH2 CH(CH3) "5-SO2 NH2 " CH3 CH2 CH2 N(SO2 CH3)CH.sub .2 CH2 K+5-SO2 NHC3 H6 OCH3 " " CH2 CH2 SO2 NHCH2 CH2 "5-SO2 NHCH3) " " CH2 CH2 SO2 N(CH3)CH.sub .2 CH2 CH.sub. 2 "5-SO2 NHC2 H5 " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "5-SO2 NHC6 H11 " " CH2 CH2 SO2 N(C6 H11)CH2 CH2 "5-SO3 C6 H5 " " CH2 CH2 CH2 CH2 N(SO2 CH3)CH2 CH2 "5-SO2 NHC6 H5 " " CH2 CH2 N(SO2 C6 H4-CH 3)CH2 CH2 "5-NHCOCH3 " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "5-SC2 H5 " " CH2 CH(Cl)CH2 "" " " CH2 CH(OH)CH2 "" " " CH2 CH(CH2 OCH3) "" " " CH.sub. 2 CH(CH2 OC6 H5) "" " " CH2 CH(OCOCH3)CH2 "" " " CH2 CH2 NHCOCH2 "" " " CH2 CH2 CONHC2 H4 "" " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "" " " CH2 CH2 NHCONHCH2 CH2 "" " " CH2 CH2 N(COCH3)CH2 CH2 "" " " CH2 CH2 N(COC6 H5)CH.sub .2 CH2 "__________________________________________________________________________
TABLE 4__________________________________________________________________________ ##STR22##R (R1)m R2 Z M__________________________________________________________________________3-CH3 2-CH3 H CH2 CH2 K+" 2-Cl " " "" 2,5-di-Cl " " "" 2,5-di-CH3 " " "" 2,5-di-OCH3 " " "" 3-OCH3 C2 H5 " "" 2-OCH3, 5-NHCOCH3 H " "3-SCH3 2-CH3, 3-Cl " " "3-C6 H5 2-OCH3, 5-Cl " " "3-C6 H4p-Cl 3-NHCOCH3 C2 H5 " "3-C6 H4o-CN 3-NHCOC2 H5 C2 H4 OCH3 " "" 3-NHCOCH2 OH CH2 C6 H5 " "" 3-NHCOCH2 OCH3 C6 H11 " "" 3-NHCOC6 H5 CH2 C6 H11 " "" 3-NHCOOC2 H5 CH2 CH2 OC6 H5 " "" 3-NHCONHC2 H5 CH2 CH2 OH " "" 3-NHCOC6 H11 CH2 CH(CH3)2 " "3-C6 H5 3-NHCOCH2 CN CH2 CH2 CH2 CH3 " "" 3-NHCOCH2 OC6 H5 CH2 CH2 OCOCH3 " "" 3-NHCOCH2 C6 H5 CH2 CH2 CONH2 " "" 3-CH3 CH2 CH2 NHCOCH3 " "" " CH2 CH2 NHSO2 CH3 " "3-C6 H4p-CH 2 " CH2 CH2 SO2 NH2 " "3-C6 H5 " CH2 CH2 CH2 SO2 CH3 " "" " CH2 CH2 SCH3 " "" H ##STR23## CH2 CH2 CH2 Na+" " ##STR24## " "" 3-OC6 H5 ##STR25## " NH4 +" 3-CH3 C6 H5 CH2 CH2 Na+" " ##STR26## CH2 CH(CH2 OC6 H5) "3-SO2 CH3 " CH2 CH2 COOCH3 CH2 CH(C6 H5) "3-SCH2 CH2 COOCH3 " CH2 CH2 CN CH2 CH(CH3) "3-SCH2 C6 H5 " C2 H5 CH2 CH(OH)CH2 "3-SCH2 CH2 OCH3 2-CH3 S H CH2 CH2 CH2 CH2 "3-SC6 H11 3-CH3 C2 H4 OC2 H4 OC2 CH2 CH(OCOCH3)CH2 "3-SC2 H5 " CH2 CH(OH)CH2 Cl CH2 CH2 "" 2-OCH3, 5-CH3 C2 H5 " "" " H CH2 CH2 OCH2 CH2 "" " H " "" " " CH2 CH2 SO2 CH2 CH2 K+3-SCH2 COOCH3 3-CH3 C2 H5 CH2 CH2 SCH2 CH2 "" " " CH2 CH2 N(SO2 CH3)CH2 CH2 "" " " CH2 CH2 NHSO2 CH2 CH2 CH2 CH2 "" " " CH2 CH2 SO2 NHCH2 CH2 "3-SCH3 " " CH2 CH2 N(COCH3)CH. sub.2 CH2 "" " " CH2 CH2 CONHC2 H4 "" " " CH2 CH2 NHCOCH2 "" " " CH2 CH2 N(SO.sub. 2 C6 H5)CH2 CH2 "3-SCH2 CH(CH3)2 " " CH2 CH2 SO2 N(CH3)CH2 CH2 "" " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " CH2 CH2 N(SO2 C6 H11)CH2 "H2" " " CH2 CH2 N(COCH3)CH. sub.2 CH2 "" " " CH2 CH(CH2 OCH3) "" " " CH2 CH(Cl)CH2 "" " " CH2 CH2 NHCONHC2 H4 "" " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "__________________________________________________________________________
TABLE 5__________________________________________________________________________ ##STR27##R (R1)m R3 R4 Z M__________________________________________________________________________3-CH3 H CH3 CH3 CH2 CH2 K+" 7-CH3 " " " "" 7-OCH3 " " " "" 7-Cl " " " "" 5-CH3, 8-OCH3 " " " "" 5,8-di-OCH3 " " " "" 5,8-di-CH3 " " " "" 5-Cl, 8-OCH3 " " " "" 8-OCH3 " " " "" 8-OC2 H5 H H " "3-SCH3 7-CH3 " " " "3-C6 H5 7-NHCOCH3 CH3 CH3 " Na+" 7-NHCOH " " " "" 7-NHCOCH2 OCH3 " " " "" 7-NHCOCH2 OC6 H5 H CH(CH3)2 " "" 7-NHCOCH2 C6 H5 " " " "" 7-NHCOCH2 Cl " " " "" 7-NHCOC6 H5 " " " "" 7-NHCOC6 H11 CH3 CH3 " "" 7-NHCONHC2 H5 " " " "" 7-NHSO2 CH3 " " " "" 7-NHCOCH2 CN " " " "C6 H4o-CN 7-NHCOCH2 OH " " " "" 7-NHCOOC2 H5 " " CH2 CH2 CH2 " ##STR28## " " " "" 8-OC4 H9n H CH3 CH2 CH2 "3-C6 H4p-CH 3 7-CH3 CH3 H " "3-C6 H4o-Cl ##STR29## " CH3 " "3-SO2 CH3 7-OC2 H5 " " " "3-SC6 H11 7-OC4 H9n " " " "3-SCH2 CH2 OCH3 7-CH3 " H " "3-SCH2 CH2 COOCH3 " " " " "3-SCH2 C6 H5 " " " CH2 CH2 CH2 CH2 "3-CH2 CH3 " " " CH2 CH2 "3-SCH2 COOCH3 " " " " "3-SCH2 CH2 COOC2 H5 " " " " "3-SCH2 CH2 COOCH(CH3)2 " " " CH2 CH2 SO2 CH2 CH2 K+3-SO2 C4 H9n " " " CH2 CH2 OCH2 CH2 "3-SCH2 CH2 CONHC4 H9n " " " CH2 CH2 SCH2 CH2 "3-SCH3 " " " CH2 CH(C6 H5) "" " " " CH2 CH(CH3) "3-SC2 H5 " " " CH2 CH(OH)CH2 "" " " " CH2 CH(Cl)CH2 "" " " " CH2 CH(CH2 OCH2 CH3) "" " " " CH2 CH(CH2 OC6 "5)" " " " CH2 CH2 N(SO2 CH3) CH2 CH2 "" " " " CH2 CH2 CH2 NHSO2 CH2 CH2 "" " " " CH2 CH2 SO2 NHCH2 CH2 "" " " " CH2 CH2 NHCOCH2 "" " " " CH2 CH2 NHCOOCH2 CH2 "" " " " CH2 CH2 COOCH2 "H2" " " " CH2 CH2 CONHC2 "4" " " " CH2 CH2 NHCONHC2 H4 "" " " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 "" " " " CH2 CH2 N(COCH3)CH.sub. 2 CH2 "" " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " " CH2 CH2 SO2 N(CH3) CH2 CH2 "__________________________________________________________________________
TABLE 6__________________________________________________________________________ ##STR30##R (R1)m R3 Z M__________________________________________________________________________3-CH3 6-CH3 H CH2 CH2 K+" H H " "" " CH3 " "" 6-CH3 " " "H " " CH2 CH2 CH2 CH2 "" 6-OCH3 " " "3-SCH3 " " CH2 CH2 "3-CH2 CH3 6-CH3 " CH2 CH2 OCH2 CH2 "3-SCH2 CH2 OCH3 " " CH2 CH2 SO2 CH2 CH2 "3-SCH2 CH2 OC2 H5 " " CH2 CH2 SCH2 CH2 "3-SCH2 CH2 COOCH3 " " CH2 CH(CH3) "3-SCH2 COOCH2 CH3 " " CH2 CH(C6 H5) "3-SCH2 C6 H5 6-OC2 H5 " CH2 CH2 "3-SC6 H11 6-NHCOCH3 " " Na+3-SCH3 6-NHCOH " " "" 6-NHCOCH2 CH2 OCH3 " " "" 6-NHCOCH2 Cl " " "" 6-NHCOCH2 CN " " "" 6-NHCOCH2 CONH.sub. 2 " " "" 6-NHCOCH2 OC6 H5 " " "3-SO2 CH3 6-NHCOOC2 H5 " " "3-SO2 C4 H9 n 6-NHCONHC2 H5 " " "3-C6 H5 6-NHCOC6 H5 " " "3-C6 H4o-CN 6-NHCOC6 H11 " " "3-C6 H4o-Cl 6-NHSO2 CH3 " " "3-C6 H4p-CH 3 6-NHCOCH2 CH2 OCOCH3 " " "3-C6 H4m-CH 3 ##STR31## " " "3-C6 H4o-CH 3 6-NHCOCH2 CH2 CH2 OH " " "3-C6 H4o-CONH 2 6-CH3 " CH2 CH2 CH2 "3-C6 H4o-CN " " CH2 CH2 "3-SCH2 CH2 OC6 H5 " " " "3-SO2 C4 H9n " " " "3-SO2 CH2 CH2 COOCH3 " " " "3-SO2 CH2 COOCH3 " " " "3-SO2 C6 H11 " " " "3-SO2 CH2 CH3 " " " "3-SO2 CH2 CH2 OCH3 " H CH2 CH(CH3) "3-SCH2 CH2 CONHC2 H4 OH " CH3 CH2 CH2 N(SO2 CH3)CH.su b.2 CH2 K+3-SCH2 CH3 " " CH2 CH2 SO2 NHCH2 CH2 "" " " CH2 CH2 SO2 N(CH3)CH.su b.2 CH2 CH2 "" " " CH2 CH2 SO2 N(C.sub. 6 H5)CH2 CH2 "" " " CH2 CH2 SO2 N(C6 H11)CH2 CH2 "" " " CH2 CH2 CH2 CH2 N(SO2 CH3)CH2 CH2 "" " " CH2 CH2 N(SO2 C6 H4p-CH 3)CH2 CH2 "" " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "3-C6 H5 " " CH2 CH(Cl)CH2 "" " " CH2 CH(OH)CH2 "" " " CH2 CH(CH2 OCH3) "" " " CH2 CH(CH2 OC6 H5) "" " " CH2 CH(OCOCH3)CH2 "" " " CH2 CH2 NHCOCH2 "" " " CH2 CH2 CONHC2 H4 "" " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "" " " CH2 CH2 NHCONHCH2 CH2 "" " " CH2 CH2 N(COCH3)CH2 CH2 "" " " CH2 CH2 N(COC6 H5)CH.su b.2 CH2 "__________________________________________________________________________
TABLE 7__________________________________________________________________________ ##STR32##R (R1)m R2 Z M__________________________________________________________________________3-CH3, 4-Br 2-CH3 H CH2 CH2 K+" 2-Cl " " "" 2,5-di-Cl " " "" 2,5-di-CH3 " " "" 2,5-di-OCH3 " " "" 3-OCH3 C2 H5 " "" 2-OCH3, 5-NHCOCH3 H " "" 2-CH3, 3-Cl " " "" 2-OCH3, 5-Cl " " "" 3-NHCOCH3 C2 H5 " "" 3-NHCOC2 H5 C2 H4 OCH3 " "" 3-NHCOCH2 OH CH2 C6 H5 " "H 3-NHCOCH2 OCH3 C6 H11 " "" 3-NHCOC6 H5 CH2 C6 H11 " "" 3-NHCOOC2 H5 CH2 CH2 OC6 H5 " "3-CH34-Cl 3-NHCONHC2 H5 CH2 CH2 OH " "" 3-NHCOC6 H11 CH2 CH(CH3)2 " "" 3-NHCOCH2 CN CH2 CH2 CH2 CH3 " "" 3-NHCOCH2 OC6 H5 CH2 CH2 OCOCH3 " "3-CH34-CN 3-NHCOCH2 C6 H5 CH2 CH2 CONH2 " "3-CH34-COOC 2 H5 3-CH3 CH2 CH2 NHCOCH3 " "" " CH2 CH2 NHSO2 CH3 " "" " CH2 CH2 SO2 NH2 " "" " CH2 CH2 CH2 SO2 CH3 " "3-CH34-SCH 2 CHCH2 " CH2 CH2 SCH3 " "" H ##STR33## CH2 CH2 CH2 Na+" " ##STR34## " "3-CH34-SO 2 C2 H5 3-OC6 H5 ##STR35## " NH4 +3-CH34-SC 6 H11 3-CH3 C6 H5 CH2 CH.sub. Na+3-CH34-OC 2 H5 " ##STR36## CH2 CH(CH2 OC6 H5) "3-Cl4-CN " CH2 CH2 COOCH3 CH2 CH(C6 H5) "3-CH34-SCN " CH2 CH2 CN CH2 CH(CH3) "3-Br4-COOCH3 " C2 H5 CH2 CH(OH)CH2 "3-CH34-COOC 2 H5 2-CH3 S H CH2 CH2 CH2 CH2 "3-CH34-CONH 2 3-CH3 C2 H4 OC2 H4 OC2 H5 CH2 CH(OCOCH3)CH2 "3-CH34-CONHC 2 H4 OH " CH2 CH(OH)CH2 Cl CH2 CH2 "3-CH34-CONHC 4 H9 -n 2-OCH3, 5-CH3 C2 H5 " "3-CH34-OC 6 H5 " H CH2 CH2 OCH2 CH2 "3-CH34-OC 6 H4p-CH 3 " H " "3-CH34-SC 6 H5 " " CH2 CH2 SCH2 CH2 K+3-CH34-SCH 2 CH2 OH 3-CH3 C2 H5 CH2 CH2 SCH2 CH2 "3-CH34-SCH 2 CH3 " " CH2 CH2 N(SO2 CH3)CH2 CH2 " ##STR37## " " CH2 CH2 NHSO2 CH2 CH2 CH2 CH2 "3-CH34-Br " " CH2 CH2 SO2 NHCH2 CH2 "" " " CH2 CH2 N(COCH3)CH 2 CH2 "" " " CH2 CH2 CONHC2 H4 "" " " CH2 CH2 NHCOCH2 "" " " CH2 CH2 N(SO2 C6 H5)CH2 "H23-CH34-CONH 2 " " CH2 CH2 SO2 N(CH3)CH2 CH2 "3-CH34-CONHC 3 H6 OCH3 " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "3-CH34-Cl " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "" " " CH2 CH2 N(COCH3)CH 2 CH2 "" " " CH2 CH(CH2 OCH3) "" " " CH2 CH(Cl)CH2 "" " " CH2 CH2 NHCONHC2 H4 "" " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "__________________________________________________________________________
TABLE 8__________________________________________________________________________ ##STR38##R (R1)m R3 R4 Z M__________________________________________________________________________3-CH34-Br H CH3 CH3 CH2 CH2 K+" 7-CH3 " " " "" 7-OCH3 " " " "" 7-Cl " " " "" 5-CH3, 8-OCH3 " " " "" 5,8-di-OCH3 " " " "" 5,8-di-CH3 " " " "" 5-Cl, 8-OCH3 " " " "" 8-OCH3 " " " "" 8-OC2 H5 H H " "" 7-CH3 " " " "3-CH34-CN 7-NHCOCH3 CH3 CH3 " Na+" 7-NHCOH " " " "" 7-NHCOCH2 OCH3 " " " "3-CH34-COOC 2 H5 7-NHCOCH2 OC6 H5 H CH(CH3)2 " "" 7-NHCOCH2 C6 H5 " " " "" 7-NHCOCH2 Cl " " " "3-CH3 7-NHCOC6 H5 " " " "" 7-NHCOC6 H11 CH3 CH3 " "3-CH34-Cl 7-NHCONHC2 H5 " " " "" 7-NHCOCH2 CN " " " "" 7-NHCOCH2 OH " " " "3-Cl-4-CN 7-NHCOOC2 H5 " " CH2 CH2 CH2 "3-Br-4-COOCH3 ##STR39## " " " "34-SCH2 CH2 OCOCH3 " " " CH2 CH2 CH2 CH2 "3-CH34-SCH 3 " " " CH2 CH2 "3-CH34-SO 2 CH3 " " " " "3-CH34-SC 6 H5 " " " " "3-CH34-SC 6 H4p-C(CH3)3 " " " CH2 CH2 SO2 CH2 CH2 K+3-CH24-SC 6 H4p-Cl " " " CH2 CH2 OCH2 CH2 " ##STR40## " " " CH2 CH2 SCH2 CH2 " ##STR41## " " " CH2 CH(C6 H5) " ##STR42## " " " CH2 CH(CH3) "3-CH34-SC 6 H11 " " " CH2 CH(OH)CH2 "3-CH34-SCN " " " CH2 CH(Cl)CH2 "3-CH34-OC 6 H5 " " " CH2 CH(CH2 OCH2 CH3) "3-CH34-OC 2 H5 " " " CH2 CH(CH2 OC6 H5)3-CH34-SCH 2 CHCH2 " " " CH2 CH2 N(SO2 CH3) CH2 CH2 "3-CH34-Br " " " CH2 CH2 CH2 NHSO2 CH2 CH2 "" " " " CH2 CH2 SO2 NHCH2 CH2" " " " CH2 CH2 NHCOCH2 "" " " " CH2 CH2 NHCOOCH2 CH2 "" " " " CH2 CH2 COOCH2 "H2" " " " CH2 CH2 CONHC2 "4" " " " CH2 CH2 NHCONHC2 H4 "" " " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 "" " " " CH2 CH2 N(COCH3)CH.sub. 2 CH2 "" " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " " CH.sub. 2 CH2 SO2 N(CH3 )CH2 CH2 "__________________________________________________________________________
TABLE 9__________________________________________________________________________ ##STR43##R (R1)m R3 Z M__________________________________________________________________________3-CH34-Cl 6-CH3 H CH2 CH2 K+" H H " "" " CH3 " "" 6-CH3 " " "3-Cl4-CN " " CH2 CH2 CH2 CH2" 6-OCH3 " " "3-CH3 " " CH2 CH2 "3-CH34-COOC 2 H5 6-CH3 " CH2 CH2 OCH.sub. 2 "H23-CH34-CONH 2 " " CH2 CH2 SO2 CH2 CH2 "3-CH34-CONHC 2 H4 OH " " CH2 CH2 SCH2 CH23-CH34-CONHC 4 H9n " " CH2 CH(CH3) "3-CH34-CONHC 3 H6 OCH3 " " CH2 CH(C6 H5) "3-CH34-CO 2 CH2 H2 OCH3 6-OC2 H5 " CH2 CH2 "3-CH34-CONHCH 3 6-NHCOCH3 " " Na+3-CH34-Br 6-NHCOH " " "" 6-NHCOCH2 CH2 OCH3 " " "" 6-NHCOCH3 Cl " " "" 6-NHCOCH2 CN " " "H 6-NHCOCH2 CONH2 " " "" 6-NHCOCH2 OC6 H5 " " "3-CH.sub. 34-SC2 H5 6-NHCOOC2 H5 " " "3-CH34-SCH 2 CH2 OH 6-NHCONHC2 H5 " " "3-CH34-SCH 2 CHCH2 6-NHCOC6 H5 " " "3-CH34-SCH 2 OCOCH3 6-NHCOC6 H11 " " "3-CH34-SC 6 H5 6-NHSO2 CH3 " " "3-CH34-SC 6 H4p-C(CH3)2 6-NHCOCH2 CH2 OCOCH3 " " "3-CH34-SC 6 H11 ##STR44## " " "3-CH34-SO 2 CH2 CH2 OH 6-NHCOCH2 CH2 CH2 OH " " "3-CH34-SO 2 CH2 CH3 6-CH3 " CH2 CH2 CH2 "3-CH34-OC 6 H5 " " CH2 CH2 "3-CH34-OC 6 H4p-OCH 3 " " " " ##STR45## " " " " ##STR46## " " " " ##STR47## " " " "3-CH34-SCH 2 CH(OH)CH2 OH " " " "3-CH34-SCH 2 COOCH3 " " " "3-CH34-OC 2 H5 " H CH2 CH(CH3) "3-CH34-Br " CH3 CH2 CH2 N(SO2 CH3)CH2 CH2 K+" " " CH2 CH2 SO2 NHCH2 CH2 "" " " CH2 CH2 SO2 N(CH3 )CH2 CH2 CH2 "" " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " CH2 CH2 SO2 N(C6 H11)CH2 CH2 "" " " CH2 CH2 CH2 CH2 N(SO2 CH3)CH2 "H2" " " CH2 CH2 N(SO2 C6 H4p-CH 3)CH2 CH2 "" " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "" " " CH2 CH(Cl)CH2 "" " " CH2 CH(OH)CH2 "" " " CH2 CH(CH2 OCH3) "" " " CH2 CH(CH2 OC6 H5) "" " " CH2 CH(OCOCH3)CH2 "" " " CH2 CH2 NHCOCH2 "" " " CH2 CH2 CONHC2 "4" " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "" " " CH2 CH2 NHCONHCH2 "" " " CH2 CH2 N(COCH3)CH.sub .2 CH2 "" " " CH2 CH2 N(COC6 H5)CH2 CH2 "__________________________________________________________________________
TABLE 10__________________________________________________________________________ ##STR48##A R (R1)m R2 Z M__________________________________________________________________________H 4-CN 2-CH3 H CH2 CH2 K+" " 2-Cl " " "" " 2,5-di-Cl " " "" " 2,5-di-CH3 " " "" " 2,5-di-OCH3 " " "" " 3-OCH3 C2 H5 " "" " 2-OCH3, H " " 5-NHCOCH3" " 2-CH3, 3-Cl " " "" " 2-OCH.sub. 3, 5-Cl " " "" " 3-NHCOCH3 C2 H5 " "" " 3-NHCOC2 H5 C2 H4 OCH3 " "" H 3-NHCOCH2 OH CH2 C6 H5 " "" " 3-NHCOCH2 OCH3 C6 H11 " "" " 3-NHCOC6 H5 CH2 C6 H11 " "" " 3-NHCOOC2 H5 CH2 CH2 OC6 H5 " "" " 3-NHCONHC2 H5 CH2 CH2 OH " "C6 H5 3-SC2 H54-CN 3-NHCOC6 H11 CH2 CH(CH3)2 " "" 3-SC2 H54-COOCH 3 3-NHCOCH2 CN CH2 CH2 CH2 CH3 " "" 3-SC2 H54-CONH 2 3-NHCOCH2 OC6 H5 CH2 CH2 OCOCH3 " "" 3-SCH34-CN 3-NHCOCH2 C6 H5 CH2 CH2 CONH2 " "" " 3-CH3 CH2 CH2 NHCOCH3 " "" " " CH2 CH2 NHSO2 CH3 " "" " " CH2 CH2 SO2 NH2 " "SO2 C6 H5 " " CH2 CH2 cH2 SO2 CH3 " "COCH3 4-CN " CH2 CH2 SCH3 " "H " H ##STR49## CH2 CH2 CH2 Na+" " " ##STR50## " "" " 3-OC6 H.sub. 5 ##STR51## " NH4 +COOC2 H5 " 3-CH3 C6 H5 CH2 CH2 Na+H " " ##STR52## CH2 CH(CH2 OC6 H5) "CH3 4-CN " CH2 CH2 COOCH3 CH2 CH(C6 H5) "" 4-COOCH3 " CH2 CH2 CN CH2 CH(CH3)" 4-CONH2 " C2 H5 CH2 CH(OH)CH2 "CH2 CH3 4-CN 2-CH3 S H CH2 CH2 CH2 CH2 "C6 H5 " 3-CH3 C2 H4 OC2 H4 OC2 H5 CH2 CH(OCOCH3)CH.sub .2 "" 4-COOCH3 " CH2 CH(OH)CH2 Cl CH2 CH2 "C6 H4p-Cl " 2-OCH3, 5-CH3 C2 H5 " "C6 H4o-CH.sub. 3 " " H CH2 CH2 OCH2 CH2 "C6 H5 " " H " "" " " " CH2 CH2 SO2 CH2 CH2 K+H 4-CONHC2 H4 OH 3-CH3 C2 H5 CH2 CH2 SCH2 CH2 "" 4-CONHC4 H9n " " CH2 CH2 N(SO2 CH3)CH2 CH2 "" 4-CONHC4 H9n " " CH2 CH2 N(SO2 CH3)CH2 CH2 "" 4-COOC2 H4 OCH.sub. 3 " " CH2 CH2 NHSO2 CH2 CH2 CH2 CH2"" 4-CONHC3 H6 OCH3 " " CH2 CH2 SO2 NHCH2 CH2 "" 4-CN " " CH2 CH2 N)COCH2 )CH2 CH2 "-" " " " CH. sub.2 CH2 CONHC2 H4 "" " " " CH2 CH2 NHCOCH2 "" " " " CH2 CCH2 N(SO2 C6 H5)CH2 CH2 "SO2 CH3 4-CN " " CH2 CH2 SO2 N(CH3)CH2 CH2 "SO2 C6 H5 " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "SO2 CH2 CH3 " " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "H " " " CH2 CH2 N(COCH3 )CH2 CH2 "" " " " CH2 CH(CH2 OCH3 ) "" " " " CH2 CH(Cl)CH2 "" " " " CH2 CH2 NHCONHC.sub. 2 H4 "" " " " CH2 CH2 NHCOOCH.sub. 2 CH2 "" " " " CH2 CH2 COOCH2 CH2 "__________________________________________________________________________
TABLE 11__________________________________________________________________________ ##STR53##A R (R1)m R3 R4 Z M__________________________________________________________________________H 4-CN H CH3 CH3 CH2 CH2 K+" " 7-CH3 " " " "" " 7-OCH3 " " " "" " 7-Cl " " " "" " 5-CH3, 8-OCH3 " " " "" " 5,8-di-OCH3 " " " "" " 5,8-di-CH3 " " " "" " 5-Cl, 8-OCH3 " " " "" " 8-OCH3 " " " "" " 8-OC2 H5 H H " "" H 7-CH3 " " " "CH3 " 7-NHCOCH3 CH3 CH3 " Na+" " 7-NHCOH " " " "H 4-COOCH3 7-NHCOCH2 OCH3 " " " "H 4-COOC2 H5 7-NHCOCH2 OC6 H5 H CH(CH3)2 " "H 4-COOC2 H4 OCH3 7-NHCOCH2 C6 H5 " " " "H 4-CONH2 7-NHCOCH2 Cl " " " "H 4-CONHC2 H5 7-NHCOC6 H5 " " " "" " 7-NHCOC6 H.sub. 11 CH3 CH3 " "" " 7-NHCONHC2 H5 " " " "C6 H5 4-CN 7-NHSO2 CH3 " " " "" " 7-NHCOCH2 CN " " " "C6 H4p-Cl " 7-NHCOCH2 OH " " " "C6 H4p-CH 3 " 7-NHCOOC2 H5 " " CH2 CH2 CH2 "SO2 CH3 " ##STR54## " " " "" 4-COOCH3 8-OC4 H.sub. 9n H CH3 CH2 CH2 "SO2 C6 H5 " 7-CH3 CH3 H " "" 4-CN ##STR55## " CH3 " "" 4-CONHC2 H4 OH 7-OC.sub. 2 H5 " " " "" 4-COOCH(CH3)2 7-OC4 H9n " " " "CH3 3-SC2 H54-CN 7-CH3 " H " "C6 H5 " " " " " "" 3-SC2 H54-COOCH 3 " " " CH2 CH2 CH2 CH2 "" 3-SCH34-COOC 2 H5 " " " CH2 CH2 "" 3-SO2 CH34-COOCH 3 " " " " "" 3-SC6 H54-COOCH 3 " " " " "COCH3 4-CN " " " CH2 CH2 SO2 CH2 CH2 K+" 4-COOCH3 " " " CH2 CH2 OCH2 CH2 "CH2 CH2 OH " " " " CH2 CH2 SCH2 CH2 "H 3-CH2 CN4-CN " " " CH2 CH(C6 H5) "H 3-CH2 CONH24-CN " " " CH2 CH(CH3) "H 4-CN " " " CH2 CH(OH)CH2 "" " " " " CH2 CH(Cl)CH2 "" " " " " CH2 CH(CH2 OCH2 CH3) "" " " " " CH2 CH(CH2 OC6 H5) "" " " " " CH2 CH2 N(SO2 CH3)CH2 CH2 "" " " " " CH2 CH2 CH2 NHSO2 CH2 CH2 "" " " " " CH2 CH2 SO2 NHCH2 CH.sub. "" " " " " CH2 CH2 NHCOCH3 "" " " " " CH2 CH2 NHCOOCH2 CH2 "" " " " " CH2 CH2 COOCH2 CH2 "" " " " " CH2 CH2 CONHC2 H4 "" " " " " CH2 CH2 NHCONHC2 H4 "" " " " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 "" " " " " CH2 CH2 N(COCH3)C H2 CH2 "" " " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " " " CH2 CH2 SO2 N(CH3)CH2 CH2 "__________________________________________________________________________
TABLE 12__________________________________________________________________________ ##STR56##A R (R1)m R3 Z M__________________________________________________________________________H 4-CN 6-CH3 H CH2 CH2 K+" " H H " "CH3 " " CH3 " "" 4-COOCH3 6-CH3 " " "" 4-COOC2 H4 OC2 H5 " " CH2 CH2 CH2 CH2 "" 4-CONH2 6-OCH3 " " "" 4-CONHC.sub. 2 H4 OH " " CH2 CH2 "" 4-CONHC3 H6 OCH3 6-CH3 " CH2 CH2 OCH2 CH2 "" 4-CONHC2 H4 NHCOCH3 " " CH2 CH2 SO2 CH2 CH2 "CH2 CH3 4-CN " " CH2 CH2 SCH2 CH2 "C6 H5 " " " CH2 CH(CH3) "" 4-COOCH2 CH3 " " CH2 CH(C6 H5) "" 4-CONH2 6-OC2 H5 " CH2 CH2 "C6 H4o-Cl " 6-NHCOCH3 " " Na+H " 6-NHCOH " " "" 4-COOCH3 6-NHCOCH2 CH2 OCH3 " " "" " 6-NHCOCH2 Cl " " "" 4-CONHC.sub. 4 H9n 6-NHCOCH2 CN " " "" " 6-NHCOCH2 CONH2 " " "" " 6-NHCOCH2 OC6 H5 " " "SO2 CH3 4-CN 6-NHCOOC2 H5 " " "" 4-COOCH3 6-NHCONHC2 H5 " " "H 3-CH2 CN4-CN 6-NHCOC6 H5 " " "C6 H5 3-SCH34-CN 6-NHCOC6 H11 " " "" 3-SCH2 CH34-CN 6-NHSO2 CH3 " " "" 3-SCH2 CH34-COOCH 3 6-NHCOCH2 CH2 OCOCH3 " " "" 3-SCH34-CONHC 4 H9n ##STR57## " " "SO2 C6 H5 4-CN 6-NHCOCH2 CH2 CH2 OH " " "" 4-COOCH3 6-CH3 " CH2 CH2 CH2 "SO2 C6 H4p-CH 3 4-CN " " CH2 CH2 "SO2 C4 H9n " " " " "COCH3 " " " " "COOC2 H5 " " " " "CH2 CH2 OH H " " " "C6 H4o-CH 3 " " " " "" 4-COOCH3 " " " "" 4-COOCH(CH3)2 " H CH2 CH(CH3) "SO2 C6 H11 " " CH3 CH2 CH2 N(SO2 CH3)CH2 CH2 K+H 4-CN " " CH2 CH2 SO2 NHCH2 CH2 "" " " " CH2 CH2 SO2 N(CH3 )CH2 CH2 CH2 "" " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " " CH2 CH2 SO2 N(C6 H11)CH2 CH2 "" " " " CH2 CH2 CH2 CH2 N(SO2 CH3)CH.su b.2 CH2 "" " " " CH2 CH2 N(SO2 C6 H4p-CH 3)CH2 CH2 "" " " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "C6 H5 " " " CH2 CH(Cl)CH2 "" " " " CH2 CH(OH)CH2 "" " " " CH2 CH(CH2 OCH3) "" " " " CH2 CH(CH2 OC6 H5) "" " " " CH2 CH(OCOCH3)CH2 "" " " " CH2 CH2 NHCOCH2 "" " " " CH2 CH2 CONHC2 H4 "" " " " CH2 CH2 NHCOOCH2 CH2 "" " " " CH2 CH2 COOCH2 CH2 "" " " " CH2 CH2 NHCONHCH2 CH2 "" " " " CH2 CH2 N(COCH3)CH. sub.2 CH2 "" " " " CH2 CH2 N(COC6 H5)CH2 CH2 "__________________________________________________________________________
TABLE 13 ##STR58##R (R1)m R2 Z M 3,5-di-CN4-CH3 2-CH3 H CH2 CH2 K+ " 2-Cl " " " " 2,5-di-Cl " " " " 2,5-di-CH3 " " " 3-CN5-C6 H5 2,5-di-OCH3 " " " 3-COOCH35-C 6 H5 3-OCH3 C2 H5 " " 3-CONH25-C 6 H5 2-OCH3, 5-NHCOCH3 H " " 3-CONHC2 H55-C 6 H5 2-CH3, 3-Cl " " " 3-COOCH3 2-OCH3, 5-Cl " " " 3-CN 3-NHCOCH3 C2 H5 " " 3-CN4-CH35-COOC 2 H5 3-NHCOC2 H5 C2 H4 OCH3 " " " 3-NHCOCH2 OH CH2 C6 H5 " " H 3-NHCOCH2 OCH3 C6 H11 " " " 3-NHCOC6 H5 CH2 C6 H11 " " 3-CN4-CH35-COCH 3 3-NHCOOC2 H5 CH2 CH2 OC6 H5 " " 3-COOCH34-CH 35-CN 3-NHCONHC2 H5 CH2 CH2 OH " " 3-COOCH34-CH 35-COC 6 H5 3-NHCOC6 H11 CH2 CN(CH3)2 " " 3-COOCH35-COC 6 H5 3-NHCOCH2 CN CH2 CH2 CH2 CH3 " " 3-COOCH35-COCH(CH3)2 3-NHCOCH2 OC6 H5 CH2 CH2 OCOCH3 " " " 3-NHCOCH2 C6 H5 CH2 CH2 CONH2 " " " 3-CH3 CH2 CH2 NHCOCH3 " " " " CH2 CH2 NHSO2 CH3 " " " " CH2 CH2 SO2 NH2 " " " " CH2 CH2 CH2 SO2 CH3 " " 3-SO2 C6 H55-COCH 3 " CH2 CH2 SCH3 " " 3-SO2 CH35-CN H ##STR59## CH2 CH2 CH2 Na+ 3-SO2 C6 H55-Br " ##STR60## " " 3,5-di-SO2 CH3 3-OC6 H5 ##STR61## " NH4 + 3,5-di-SO2 NH2 3-CH3 C6 H5 CH2 CH2 Na+ 3,5-di-SO2 N(C2 H5)2 " ##STR62## CH2 CH(CH2 OC6 H5) " 3-CN5-COCH3 " CH2 CH2 COOCH3 CH2 CH(C6 H5) " 3-CN5-COCH(CH3)2 " CH2 CH2 CN CH2 CH(CH3) " 3-CNSCOOC2 H5 " C2 H5 CH2 CH(OH)CH2 " 3-CONH25-COOC 2 H5 2-CH3 S H CH2 CH2 CH2 CH2 " 3-CONH25-COCH(CH3)2 3-CH3 C2 H4 OC.sub. 2 H4 OC2 H5 CH2 CH(OCOCH3)CH2 " 3-CONHC2 H4 OH5-COCH(CH3)2 " CH2 CH(OH)CH2 Cl CH2 CH2 " " 2-OCH3, 5-CH3 C2 H5 " " " " H CH2 CH2 OCH2 CH2 " " " H " " " " " CH2 CH2 SO2 CH2 CH2 K+ 3-CONHC3 H6 OCH3SCOCH(CH3)2 3-CH3 C2 H5 CH2 CH2 SCH2 CH2 " 3-CONHC4 H9n-5-COCH(CH3)2 " " CH2 CH2 N(SO2 CH3)CH2 CH2 " 3-CONHC2 H4 OH5-COCH(CH3)2 " " CH2 CH2 NHSO2 CH2 CH2 CH2 CH2 " 3-COOCH35-SO 2 CH3 " " CH2 CH2 SO2 NHCH2 CH2 " 3-CONHC2 H55-SO 2 CH3 " " CH2 CH2 N(COCH3)CH2 CH2 " 3-CONH25-SO 2 CH3 " " CH2 CH2 CONHC2 H4 " 3-CONH25-SO 2 C4 H9n " " CH2 CH2 NHCOCH2 " 3-COOCH34-CH 35-SCN " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 " 3-CHO4-CH3 " " CH2 CH2 SO2 N(CH3)CH2 CH2 " 3-CONH25-C 6 H4p-CH 3 " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 " 3-CN5-COOC2 H5 " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 " 3-COOCH35-COCH(CH3)2 " " CH2 CH2 N(COCH3)CH2 CH2 " " " " CH2 CH(CH2 OCH3) " " " " CH2 CH(Cl)CH2 " " " " CH2 CH2 NHCONHC2 H4 " " " " CH2 CH2 NHCOOCH2 CH2 " " " " CH2 CH2 COOCH2 CH2 "
TABLE 14__________________________________________________________________________ ##STR63## R (R1)m R3 R4 Z M__________________________________________________________________________3-CONHC2 H55-COCH(CH3)2 H CH3 CH3 CH2 CH2 K+" 7-CH3 " " " "3-CONH25-COCH(CH3)2 7-OCH3 " " " "" 7-Cl " " " "" 5-CH3, 8-OCH3 " " " "" 5,8-di-OCH3 " " " "" 5,8-di-CH3 " " " "" 5-Cl, 8-OCH3 " " " "" 8-OCH3 " " " "H 8-OC2 H5 H H " "" 7-CH3 " " " "3-COOCH35-COCH(CH3)2 7-NHCOCH3 CH3 CH3 " Na+" 7-NHCOH " " " "" 7-NHCOCH2 OCH3 " " " "" 7-NHCOCH2 OC6 H5 H CH(CH3)2 " "" 7-NHCOCH2 C6 H5 " " " "3,5-di-CN4-CH3 7-NHCOCH2 Cl " " " "" 7-NHCOC6 H5 " " " "" 7-NHCOC6 H11 CH3 CH3 " "" 7-NHCONHC2 H5 " " " "" 7-NHSO2 CH3 " " " "3-CONH25-C 6 H5 7-NHCOCH2 CN " " " "" 7-NHCOCH2 OH " " " "3-COOCH35-C 6 H5 7-NHCOOC2 H5 " " CH2 CH2 CH2 "3-COOCH35-COCH 3 ##STR64## " " " "3-CN5-COOC2 H5 8-OC4 H9n H CH3 CH2 CH2 "3-CN4-CH35-COOC 2 H5 7-CH3 CH3 H " "3-CN4-CH35-COCH 3 ##STR65## " CH3 " "3-COOCH34-CH 35-CN 7-OC2 H5 " " " "3-CN4-CH35-CO 2 CH2 CH2 OC2 H5 7-OC4 H9n " " " "3-SO2 C6 H55-COCH 3 7-CH3 " H " "3-SO2 C6 H4p-Cl5-COCH 3 " " " " "3-SO2 CH35-CN " " " CH2 CH2 CH2 CH2 "3-COOCH35-Br " " " CH2 CH2 "3-COOCH35-SCN " " " " "3-CONHC2 H4 OH5-COCH(CH3)2 " " " " "3-CONHC3 H6 OCH35-COCH(CH3)2 " " " CH2 CH2 SO2 CH2 CH2 K+3-CN5-SO2 CH3 " " " CH2 CH2 OCH2 CH2 "3,5-di-SO2 NH2 " " " CH2 CH2 SCH2 CH2 "3,5-di-SO2 NHC2 H5 " " " CH2 CH(C6 H.sub. ")3-COOCH35-COC 6 H5 " " " CH2 CH(CH3) "3-CONHC4 H9n-5-COC 6 H5 " " " CH2 CH(OH)CH2 "3-COOCH35-SO 2 CH3 " " " CH2 CH(Cl)CH2 "3-CONHC2 H4 OH5-SO2 CH3 " " " CH2 CH(CH2 OCH2 CH3) "3-CHO " " " CH2 CH(CH2 OC6 H5) "3-SO2 C6 H5 " " " CH2 CH2 N(SO2 CH3)CH2 CH2 "3-CONHC2 H55-COCH(CH3)2 " " " CH2 CH2 CH2 NHSO2 CH2 CH2 "" " " " CH2 CH2 SO2 NHCH2 CH2 "" " " " CH2 CH2 NHCOCH2 "" " " " CH2 CH2 NHCOOCH2 CH2 "" " " " CH2 CH2 COOCH2 CH2 "" " " " CH2 CH2 CONHC2 H4 "" " " " CH2 CH2 NHCONHC2 H4 "" " " " CH2 CH2 N(SO2 C6 H5)CH2 CH2 "" " " " CH2 CH2 N(COCH3)C H2 CH2 "3-COOCH34-CH 35-CONH 2 " " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " " CH2 CH2 SO2 N(CH3)CH2 CH2 "__________________________________________________________________________
TABLE 15__________________________________________________________________________ ##STR66##R (R1)m R3 Z M__________________________________________________________________________3-COOCH35-COCH(CH3)2 6-CH3 H CH2 CH2 K+3-CONH25-COCH(CH3)2 H H " "3-CN5-COCH(CH3)2 " CH3 " "" 6-CH3 " " "3-CONH25-C 6 H5 " " CH2 CH2 CH2 CH2 "" 6-OCH3 " " "" " " CH2 CH2 "3-CN5-C.sub. 6 H5 6-CH3 " CH2 CH2 OCH2 CH2 "3-CONHC2 H4 OH5-C6 H5 " " CH2 CH2 SO2 CH2 CH2 "3-CONHC2 H55-COC 6 H5 " " CH2 CH2 SCH2 CH2 "3-CONHCH35-COC 6 H5 " " CH2 CH(CH3) "3-CN4-CH35-COOC 2 H5 " " CH2 CH(C6 H5) "3-CN4-CH35-COOC 2 H4 OCH3 6-OC2 H5 " CH2 CH2 "3-CHO4,5-di-CH3 6-NHCOCH3 " " Na+3-CN4-CH35-SCH 3 6-NHCOH " " "3-COOCH34-CH 35-CONH 2 6-NHCOCH2 CH2 OCH3 " " "3-CONH24-CH 35-CN 6-NHCOCH2 Cl " " "3,5-di-CN4-CH3 6-NHCOCH2 CN " " "" 6-NHCOCH2 CONH2 " " "H 6-NHCOCH2 OC6 H5 " " "" 6-NHCOOC2 H5 " " "3-CONH24-CH 35-COOCH 3 6-NHCONHC2 H5 " " "3-SO2 CH35-COCH 3 6-NHCOC6 H5 " " "3-SO2 C6 H55-COCH 3 6-NHCOC6 H11 " " "3-SO2 C6 H4p-Cl5-COCH 3 6-NHSO2 CH3 " " "3-SO2 CH35-Br 6-NHCOCH2 CH2 OCOCH3 " " "3,5-di-SO2 CH3 ##STR67## " " "3,5-di-SO2 NH2 6-NHCOCH2 CH2 CH2 OH " " "3,5-di-SO2 NHC2 H5 6-CH3 " CH2 CH2 CH2 "3-CONHC2 H4 OH5-COCH(CH3)2 " " CH2 CH2 "3-CONHC3 H6 OCH35-COCH(CH3)2 " " " "3-CONHC2 H4 NHCOCH3 " " " "3-CONHC4 H9n-5-C 6 H5 " " " "3-CN5-COOC2 H5 " " " "3-CN4-CH35-COOCH(CH3)2 " " " "3-CN4-CH35-CONHC 2 H5 " " " "3-CN4-CH35-CONHC 6 H5 " H CH2 CH(CH3) "3-CONH25-SO 2 CH3 " CH3 CH2 CH2 N(SO2 CH3)CH2 CH2 K+3-CONH25-COCH(CH3)2 " " CH2 CH2 SO2 NHCH2 CH2 "" " " CH2 CH2 SO2 N(CH3 )CH2 CH2 CH2 "" " " CH2 CH2 SO2 N(C6 H5)CH2 CH2 "" " " CH2 CH2 SO2 N(C6 H11)CH2 CH2 "" " " CH2 CH2 CH2 CH2 N(SO2 CH3)CH2 "H2" " " CH2 CH2 N(SO2 C6 H4p-CH 3)CH2 CH2 "3-CONHC2 H55-COCH(CH3)2 " " CH2 CH2 N(SO2 C6 H11)CH2 CH2 "" " " CH2 CH(Cl)CH2 "" " " CH2 CH(OH)CH2 "" " " CH2 CH(CH2 OCH3) "" " " CH2 CH(CH2 OC6 H5) "" " " CH2 CH(OCOCH3 "CH2" " " CH2 CH2 NHCOCH2 "" " " CH2 CH2 CONHC2 "4" " " CH2 CH2 NHCOOCH2 CH2 "" " " CH2 CH2 COOCH2 CH2 "" " " CH2 CH2 NHCONHCH2 CH2 "" " " CH2 CH2 N(COCH3)CH.sub .2 CH2 "" " " CH2 CH2 N(COC6 H5)CH2 CH2 "__________________________________________________________________________
The invention has been described in detail with particular reference to preferred embodiments thereof, but it will be understood that variations and modifications can be effected within the spirit and scope of the invention.
| 标题 | 发布/更新时间 | 阅读量 |
|---|---|---|
| 一种镉污染土壤改良剂及其制备方法和镉污染土壤改良方法 | 2020-05-08 | 151 |
| 增塑剂组合物、树脂组合物及其制备方法 | 2020-05-11 | 267 |
| 一种提高土壤硝态氮微生物同化效率的方法 | 2020-05-11 | 344 |
| 一种环氧类增塑剂及其制备方法 | 2020-05-12 | 170 |
| 增塑剂组合物和包含该增塑剂组合物的树脂组合物 | 2020-05-13 | 82 |
| 增塑剂组合物、树脂组合物及其制备方法 | 2020-05-13 | 139 |
| 一种氨基酸修饰光引发剂及制备方法 | 2020-05-08 | 86 |
| 一种电催化膜反应器耦合纳滤处理富砷水的方法 | 2020-05-12 | 616 |
| 一种基于TPM的软件密钥保护方法 | 2020-05-12 | 82 |
| 一种PVC家具膜水性喷印油墨及其制备方法 | 2020-05-12 | 193 |
高效检索全球专利专利汇是专利免费检索,专利查询,专利分析-国家发明专利查询检索分析平台，是提供专利分析，专利查询，专利检索等数据服务功能的知识产权数据服务商。
我们的产品包含105个国家的1.26亿组数据，免费查、免费专利分析。
专利汇分析报告产品可以对行业情报数据进行梳理分析，涉及维度包括行业专利基本状况分析、地域分析、技术分析、发明人分析、申请人分析、专利权人分析、失效分析、核心专利分析、法律分析、研发重点分析、企业专利处境分析、技术处境分析、专利寿命分析、企业定位分析、引证分析等超过60个分析角度，系统通过AI智能系统对图表进行解读，只需1分钟，一键生成行业专利分析报告。
