首页> 外国专利> 'n - (1 hpyrazol-1-yl) aryl -1 h -indole or 1 h-indazol-3-carboxamide derivatives, their preparation and application in therapeutics'

'n - (1 hpyrazol-1-yl) aryl -1 h -indole or 1 h-indazol-3-carboxamide derivatives, their preparation and application in therapeutics'

机译:“ n-[[(1-吡唑-1-基)芳基] -1 h-吲哚或1 h-吲唑-3-羧酰胺衍生物,其制备和在治疗中的应用”

摘要

N-[(1H-Pyrazol-1-yl)aryl]-1H-indole or 1H-indazole-3-carboxamide derivatives (I) are new. N-[(1H-Pyrazol-1-yl)aryl]-1H-indole or 1H-indazole-3-carboxamide derivatives of formula (I) in the form of a base or addition salt to an acid or base, are new. X : -CH or N; A : aromatic bivalent group comprising phenyl group of formula (a), pyrimidine, pyrazine or pyridazine; R1 : 1-4C alkyl or 1-4C alkoxy; R2 : Alk; R3 : OH or -NR7R8; R4 : H, halo, CN, phenyl, Alk, OAlk or -NR9R10; R5 : H, halo or Alk; R6 : H, halo, CN, -COOAlk or -CONH 2; either R7 : H or 1-4C alkyl; and R8 : 3-6C heterocycloalkyl (optionally substituted by 1-4C alkyl or -COOAlk), heteroaryl (optionally substituted by 1-4C alkyl), 3-7C cycloalkyl, 3-6C heterocycloalkyl (optionally substituted by 1-4C alkyl or -COOAlk), H, OH, OAlk or -SO 2Alk; or R7R8+N : optionally saturated, mono- or poly-cyclic, condensed or bridged 4-10C heterocycle ring comprising 1-3 other nitrogen atoms or another heteroatom comprising O or S, where the heterocycle is optionally substituted by 1-3 substituents of halo, OH, -OR11, oxo, -NR9R10, -NR12COR13, -NR12COOR13, -COR13, -COOR13, -CONR14R15, 3-7C cycloalkyl (optionally substituted with OH or 1-4C alkyl), 3-6C heterocycloalkyl (optionally substituted with 1 or 2 oxo groups), phenyl (optionally substituted by one or more substituents of halo, Alk or OAlk), pyridinyl or 1-4C alkyl (optionally substituted by one or more substituents of halo, OH, -OR11, -NR9R10, -NR12COR13, -COOR13, -CONR14R15, -SO 2Alk, 3-7C cycloalkyl, 3-6C heterocycloalkyl, phenyl (optionally substituted by one or more substituents of halo, Alk or OAlk) or heteroaryl (optionally substituted by 1-4C alkyl)); R9, R10 : H or 1-4C alkyl; R11 : Alk, 1-4C alkylene-OH or 1-4C alkylene-OAlk; R12 : H or 1-4C alkyl; R13 : 1-4C alkyl; either R14, R15 : H, 1-4C alkyl or 3-7C cycloalkyl; or R14, R15+N : heterocyclic group comprising azetidin-1-yl, pyrrolidin-1-yl, piperidin-1-yl, morpholin-4-yl or piperazin-1-yl; and Alk : 1-4C alkyl (optionally substituted by F). Independent claims are included for: (1) a pyrazole compound of formula (II); and (2) the preparation of (I). Z : 1-4C alkyl. [Image] [Image] [Image] ACTIVITY : Antianginal; Cardiant; Anticoagulant; Thrombolytic; Antiarteriosclerotic; Cerebroprotective; Vasotropic; Vulnerary; Cardiovascular-Gen.; Dermatological; Hemostatic; Immunosuppressive; Gynecological; Antiinflammatory; Nephrotropic; Gastrointestinal-Gen. MECHANISM OF ACTION : Purinergic receptor P2Y G-protein coupled 12 (P2Y12) antagonist.
机译:N-[((1H-吡唑-1-基)芳基] -1H-吲哚或1H-吲唑-3-羧酰胺衍生物(I)是新的。以酸或碱的加成盐或加成盐形式的式(I)的N-[(1H-吡唑-1-基)芳基] -1H-吲哚或1H-吲唑-3-甲酰胺衍生物是新的。 X:-CH或N; A:包含式(a)的苯基,嘧啶,吡嗪或哒嗪的芳香族二价基团; R1:1-4C烷基或1-4C烷氧基; R2:Alk; R3:OH或-NR7R8; R4:H,卤素,CN,苯基,Alk,OAlk或-NR9R10; R5:H,卤素或Alk; R6:H,卤素,CN,-COOAlk或-CONH 2; R7:H或1-4C烷基;或和R8:3-6C杂环烷基(任选地被1-4C烷基或-COOAlk取代),杂芳基(任选地被1-4C烷基取代),3-7C环烷基,3-6C杂环烷基(任选地被1-4C烷基取代或- COOAlk),H,OH,OAlk或-SO 2烷基;或R 7 R 8 + N:任选地包含1-3个其他氮原子的饱和,单环或多环,稠合或桥连的4-10C杂环,或包含O或S的另一个杂原子,其中所述杂环任选地被1-3个取代基取代卤素,OH,-OR11,氧代,-NR9R10,-NR12COR13,-NR12COOR13,-COR13,-COOR13,-CONR14R15、3-7C环烷基(可选被OH或1-4C烷基取代),3-6C杂环烷基(可选被取代)带有1或2个氧代基团),苯基(可选被一个或多个卤素,烷基或OAlk取代基取代),吡啶基或1-4C烷基(可选被一个或多个卤素,OH,-OR11,-NR9R10取代基, -NR12COR13,-COOR13,-CONR14R15,-SO 2 Alk,3-7C环烷基,3-6C杂环烷基,苯基(可选被一个或多个卤素,Alk或OAlk取代基取代)或杂芳基(可选被1-4C烷基取代) ); R9,R10:H或1-4C烷基; R11:Alk,1-4C亚烷基-OH或1-4C亚烷基-OAlk; R12:H或1-4C烷基; R13:1-4C烷基; R14,R15:H,1-4C烷基或3-7C环烷基;或R14,R15 + N:包含氮杂环丁烷-1-基,吡咯烷-1-基,哌啶-1-基,吗啉-4-基或哌嗪-1-基的杂环基;或Alk:1-4C烷基(任选地被F取代)。包括以下独立权利要求:(1)式(II)的吡唑化合物; (2)制备(I)。 Z:1-4C烷基。 [图像] [图像] [图像]活动:抗心绞痛;卡迪恩抗凝物;溶栓;抗动脉硬化;脑保护变压性伤药;心血管创皮肤;止血药免疫抑制妇科消炎(药;嗜肾胃肠源。作用机理:嘌呤能受体P2Y G蛋白偶联12(P2Y12)拮抗剂。

著录项

  • 公开/公告号BR112013032803A2

    专利类型

  • 公开/公告日2017-01-31

    原文格式PDF

  • 申请/专利权人 SANOFI;

    申请/专利号BR20131132803

  • 申请日2011-09-13

  • 分类号A61K31/455;A61K31/439;A61K31/497;A61K31/501;A61K31/506;A61P9;C07D403/12;C07D403/14;C07D405/14;C07D409/14;C07D413/14;C07D471/04;C07D471/08;C07D487/04;C07D487/08;

  • 国家 BR

  • 入库时间 2022-08-21 13:40:43

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