序号 专利名 申请号 申请日 公开(公告)号 公开(公告)日 发明人
41 Pyridone-methide azo dye JP27148796 1996-09-20 JPH09124956A 1997-05-13 RAINAA HANPUREHITO
PROBLEM TO BE SOLVED: To obtain a compound being a pyridone-methide azo dye or corresponding to its tautomer and suitably used in dyeing or printing natural or synthetic materials by selecting a specified compound. SOLUTION: This compound is the one which, in the form of a free acid, is represented by the formula (wherein D is a residue of a carboxcyclic or heterocyclic diazo component; A 1 and A 2 are each H, a substituent typical of pyridone or the like; A 3 and A 4 are each an electron-attracting residue; provided that they may be combined with each other to form a cyclic methylene active compound or the like; A 5 is H, T, OT 1, NH 2, NHT, NT 2, NHCOH, NHCOT, N=CHT, N=CT 2 or NHSO 2OT (wherein T 1 is an alkyl, a cycloalkyl or an aralkyl; T is T 1, an alkenyl, an alkynyl, an aryl or a hetrayl) or the like; X is O, NH, NT, NCOT, NCO 2T or NSO 2T, K + is NH 3 +, NHT 2T +, NH 2 +, NT 3 + or a cycloimmonium ion; B - is an anion; Z is a fiber-reactive group; (l) is 0-2; (m) is 0-8; and (n) is 0-6) or corresponding to its tautomer. COPYRIGHT: (C)1997,JPO
42 Propenoic acid derivative, manufacture and fungicidal composition JP2671088 1988-02-09 JPS63216848A 1988-09-09 JIYON MAACHIN KUROU; KURISUTOFUAA RICHIYAADO AIRESU; POORU JIYON DO FUREINU; BUIBUIENNU MAAGARETSUTO ANTONI; MAIKERU GOODON HATSUCHINGUSU
43 Production of alpha-pyridone derivative JP11822886 1986-05-22 JPS6345256A 1988-02-26 GOTO YUKIHISA; MASAMOTO KAZUHISA
PURPOSE: To obtain the titled compound useful as pharmaceuticals, agricultural chemicals or their intermediates, in high yield and selectivity, by using a reaction product of 3-benzylaminocrotonanilide and diketene as a starting substance and treating the substance with an acid in a proper solvent. CONSTITUTION: The objective compound of formula II is produced by treating the compound of formula I (R 1 is H, alkyl, cycloalkyl, aralkyl, aryl or heterocyclic group; R 2 and R 2' are R 1, alkoxy or alkenyloxy; R 3 is R 1 excluding H or alkenyl, alkynyl, etc.) with an organic acid, inorganic acid, a cation exchange resin, etc., in a proper solvent at a temperature between -20°C and the boiling point of the solvent, preferably at 0W40°C. The starting compound of formula I can be easily produced by producing the compound of formula IV by dehydrative condensation of the compound of formula III and the compound of formula R 2R 2'NH and reacting the obtained compound of formula IV with diketene in the presence of a nitrogen-containing organic compound. COPYRIGHT: (C)1988,JPO&Japio
44 JPS50132191A - JP4132474 1974-04-11 JPS50132191A 1975-10-20
45 New methine compounds and functional thin film using the same JP2002297825 2002-10-10 JP4259845B2 2009-04-30 浩 土屋; 功一 坂巻; 清 武捨
46 Pyridone - Mechidoazo dye JP27148796 1996-09-20 JP4257872B2 2009-04-22 ライナー・ハンプレヒト
47 Composition comprising a monomer compound that exhibits optical properties, the use of said composition, a polymer containing a monomer compound and the monomer compound, and the use thereof JP2007504437 2005-02-28 JP2007530514A 2007-11-01 ティモ・ルーカス
本発明は、生理学的に許容可能な媒体中に、光学的特性を呈する少なくとも1種の新規なモノマー化合物を含む少なくとも1種のポリマーを含む化粧品組成物又は医薬組成物に関する。 本発明はまた、前記化粧品組成物をケラチン質、特に、体若しくは顔の皮膚、唇、爪、睫毛、眉毛、及び/又は毛髪などに適用することを含む、ケラチン質をメイクアップ又はケアする化粧方法にも関する。 光学的特性を呈する新規なモノマー化合物、前記化合物を含むポリマー、及び組成物に光学的特性、特に、蛍光又は蛍光増白特性をもたせるための組成物中におけるそれらの使用も開示している。
48 Derivatives of pyridone and its use JP2005510535 2003-11-14 JP2007510618A 2007-04-26 イー、シャンフィー
本発明により、N−置換−2(1H)ピリドンまたはその薬学的に許容される塩、およびこの化合物を含む薬学的調製物が提供される。 本発明の化合物は、種々の線維症疾患、例えば、肝線維症を効率よく処置するために使用することができる。
【選択図】なし
49 Novel mono - acylated o- phenylenediamine derivative JP2005518418 2004-02-05 JP2006516553A 2006-07-06 クビエス,マンフレト; バイドナー,ミハエル; フェルティヒ,ゲオルク; ヘルティンク,フランク; ライフ,ウルリケ; リンベルク,アンヤ
本発明の目的は、式 (A) の新規なモノ-アシル化o-フェニレンジアミン誘導体およびそれらの薬学上許容される塩、ならびにこれらの化合物を製造する方法、このような化合物を含有する医薬組成物および癌のような疾患を治療するための薬剤の製造におけるそれらの使用である:
式中、Arはチオフェン-2,5-ジイル、ピリジン-2,5-ジイル、ピリジン-5,2-ジイル、ピリジン-2,6-ジイル、ピリジン-2,4-ジイルまたは1,4-フェニレンであり、R 1およびR 2は互いに独立して素、C 1-12アルキル、C 2-12アルケニル、C 2-12アルキニル、C 3-12シクロアルキルであり、前記アルキル、アルケニル、アルキニルおよびシクロアルキル基はヒドロキシ、ハロゲン、C 3-12シクロアルキル、アルコキシ、アルキルスルファニル、アシロキシ、アルコキシカルボニル、アシル、C 1-6アルキル-NH-C(O)-、C 1-6アルキル-C(O) NH-、または-NR 3 R 4により1回〜多数回置換されていてもよいか、あるいはR 1は水素であり、そしてR 2はヒドロキシル、アルコキシ、C 2-12アルケニルオキシまたはフェノキシであり、前記フェノキシ基はメチル、メトキシ、ハロゲン、ニトロ、シアノ、トリフルオロメチル、エテニルまたは-C(O)-O-CH 3により置換されていてもよく、ただしR 2がヒドロキシである場合、Arはチオフェン-2,5-ジイルではなく、そしてR 3およびR 4は互いに独立して水素またはC 1-6アルキルであるか、あるいはR 3およびR 4はそれらが結合する窒素原子と一緒になって環を形成し、前記環はオキソで一置換されており、そして前記環はそれ以上の異種原子を含有することができる。
【化1】
50 New methine compound and functional thin film using the same JP2002297825 2002-10-10 JP2004131427A 2004-04-30 TSUCHIYA HIROSHI; SAKAMAKI KOICHI; TAKESUTE KIYOSHI
PROBLEM TO BE SOLVED: To provide a new compound useful as a material for organic electroluminescent devices capable of giving the organic electroluminescent devices excellent in stability, durability, emission luminance and luminous efficiency, to provide the material comprising the compound, and to provide the organic electroluminescent devices using the material. SOLUTION: The new methine compound is represented by the general formula(I)( wherein, R 1 and R 2 are each H or a substituent; L 1 and L 2 are each an atomic group constituting a π-electron conjugated system; L 2 and L 3 are each a methine group or substituted methine group; and m and n are each 1 or 2 ). The material for organic electroluminescent devices comprises the new methine compound. The organic electroluminescent device is such as to have one or more organic thin film layers including a luminescent layer between a pair of electrodes, wherein at least one of the organic thin film layers contains one or more of this new methine compound. COPYRIGHT: (C)2004,JPO
51 Diagnostic test solution for a preservative mixture JP15954595 1995-06-26 JP2885666B2 1999-04-26 ANGERIKA KURUREEUAITENHIRAA; AKUSERU SHUMITSUTO
52 And based on the trifluoromethyl pyridone, methine - and azamethine dye JP51567796 1995-10-31 JPH10508641A 1998-08-25 ヨハン シュミット アンドレアス; エツバッハ カール−ハインツ; ゼーンス リューディガー
(57)【要約】 式 [式中、Xは窒素又はCHを表わし、R 1は、5員又は6員の炭素環式又は複素環式基を表わし、R 2は、シアノ、カルバモイル、C 1 〜C 6 −アルコキシカルボニル又はC 1 〜C 4 −アルカノイルを表わし、R 3は、場合により置換されたC 1 〜C 13 −アルキル、場合により置換されたフェニル又は場合により置換されたアミノを表わす]のピリドン染料、その熱転写法並びに新規染料を用いて合成材料を浸染又は捺染する方法。
53 Propeonic acid derivative, its production and bactericidal composition containing the same JP5640395 1995-02-09 JPH092906A 1997-01-07 JIYON MAACHIN KUROU; KURISUTOFUAA RICHIYAADO AIRESU; POORU JIYON DO FUREINU; BUIBUIENNU MAAGARETSUTO ANTONI; MAIKERU GOODON HATSUCHINGUSU
PURPOSE: To obtain a new propeonic acid derivative useful as a bactericidal agent to exterminate an infection caused by plant bacteria. CONSTITUTION: This propeonic acid derivative is a compound of formula I [Y is O, S, etc.; R<2> , R<3> are each H, an alkyl, etc.; X is a halogen, an alkyl, an alkenyl, etc.; (n) is 0, 1-4; R<1> is an aryl]) or its derivative, or a compound of formula II [in the case of an (E) isomer, Ab is 2-bromo, 3-iodo, 2-ethyl, 3-amino, 4-phenyl, etc.], e.g. (E)-methyl 2-[2-(3-chlorophenoxymethyl)phenyl]-3- methoxypropenoate. The compound of formula I is obtained by treating a compound of formula III (R<5> is a metal atom) with a compound of the formula: CH3 L (L is a liberative group), removing methanol component from a compound of formula IV, treating a ketoester of formula V with a methoxymethylating reagent, etc.
54 Preparation of α- pyridone derivative JP11822886 1986-05-22 JPH0717607B2 1995-03-01 幸久 後藤; 和久 正本
55 Silver halide imaging material JP421993 1993-01-13 JPH05271195A 1993-10-19 Kevin P Hall; Andrew W Mott; アンドリュー・ウィリアム・モット; ケビン・ピーター・ホール
PURPOSE: To obtain the subject new compound which is useful as an acutance, antihalation and filter dye for silver halide imaging material, and comprised of a specified diphenoxyalkane derivative, etc., having a substituent including a heterocycle. CONSTITUTION: A dialdehyde compound expressed by formula I (Y is a bivalent aliphatic bond), for example, 4,4-diformyl-1,2-diphenoxyethane, etc., or a compound of formula II (R is H or an alkyl) is allowed to react with a compound expressed by formula III (A is a non-metallic atom necessary to complete heterocyclic ring in which at least one of ring constitutive atoms is nitrogen) and a compound expressed by formula IV (A is similar with B), for example, 3- methyl-1,4-sulfophenyl-5-pyrazolone, etc.) in the solution at 50-90°C in the presence of a tertiary amine to obtain the objective compound useful as silver halide imaging material having a nucleus expressed by formula V or formula VI. COPYRIGHT: (C)1993,JPO
56 JPH056181B2 - JP26579188 1988-10-20 JPH056181B2 1993-01-26 MYAZAKI HAJIME; TAKAI HIDEYUKI; GO SHINTETSU; INAI KAZUFUMI
57 JPS50154272A - JP6321174 1974-06-04 JPS50154272A 1975-12-12
58 2-할로피리딘-엔-옥사이드의 제조방법 KR1020030027253 2003-04-29 KR100492402B1 2005-05-30 정재훈; 라종규; 황병돈; 이연식; 이상희; 문숙영
본 발명은 2-할로피리딘-N-옥사이드의 제조방법에 관한 것으로, 강산성 양이온교환수지 촉매 존재하에, 2-할로피리딘 1당량을 초산 1.0~1.5 당량, 과산화수소 1.0~2.5 당량과 반응시킴을 특징으로 한다.
59 2-할로피리딘-엔-옥사이드의 제조방법 KR1020030027253 2003-04-29 KR1020040092844A 2004-11-04 정재훈; 라종규; 황병돈; 이연식; 이상희; 문숙영
PURPOSE: A method for preparing 2-halopyridine-N-oxide is provided, thereby improving the preparation yield and reducing the preparation cost. CONSTITUTION: The method for preparing 2-halopyridine-N-oxide comprises reacting 1 equivalent of 2-halopyridine with 1.0 to 1.5 equivalent of acetic acid and 1.0 to 2.5 equivalent of hydrogen peroxide in the presence of strong acid cation exchange resin catalyst, wherein the amount of the strong acid cation exchange resin is 0.2 to 0.5g per 1g of 2-halopyridine; and the reaction temperature is 70 to 100 deg. C; and the reaction time is 3 hours.
60 살균제 KR1019880001176 1988-02-09 KR100111766B1 1997-02-05 존마틴클라우; 크리스토퍼리차드에일스고드프레이; 파울존드프레인; 비비엔마가레트앤토니; 미켈고돈헛칭스
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