首页> 外国专利> '6- (6-nh-substituted-triazolopyridazine sulfanyl) benzothiazoles and benzimidazole derivatives: preparation, use as medicines and use as inhibitors of met'

'6- (6-nh-substituted-triazolopyridazine sulfanyl) benzothiazoles and benzimidazole derivatives: preparation, use as medicines and use as inhibitors of met'

机译:“ 6-(6-nh-取代的三唑并吡啶嗪硫烷基)苯并噻唑和苯并咪唑衍生物:制备,用作药物和用作met的抑制剂”

摘要

The invention relates to novel products of the formula (I) where: (II) is a single or double bond; Rb is a hydrogen or fluorine atom; Ra is a NH-Rc radical in which Rc is an optionally substituted heterocycloalkyl, aryl, heteroaryl or -alkylcycloalkyl radical; X is S, SO, or SO2; A is NH or S; W is H, alkyl, or COR with R being cycloalkyl; alkyl; alkoxy; O-phenyl; O (CH2)n-phenyl with n=1 to 4; or NR1R2 with R1 being H or alk and R2 is H, cycloalkyl or alkyl; or R1, R2 form a cycle together with N optionally containing O, S, N and/or NH; all of said radicals being optionally substituted; wherein said products can be in any isomer or salt form, and can be used as drugs, in particular as MET inhibitors.
机译:本发明涉及式(I)的新产物,其中:(II)是单键或双键; Rb是氢或氟原子; Ra是NH-Rc基团,其中Rc是任选取代的杂环烷基,芳基,杂芳基或-烷基环烷基; X是S,SO或SO2; A为NH或S; W为H,烷基或COR,R为环烷基;烷基;烷氧基邻苯基O(CH 2)n-苯基,n = 1至4;或NR 1 R 2,其中R 1为H或烷基且R 2为H,环烷基或烷基;或或R 1,R 2与任选地包含O,S,N和/或NH的N一起形成一个环;所有所述基团被任选取代;其中所述产物可以是任何异构体或盐形式,并且可以用作药物,特别是用作MET抑制剂。

著录项

  • 公开/公告号BRPI1008188A2

    专利类型

  • 公开/公告日2016-03-08

    原文格式PDF

  • 申请/专利权人 SANOFI;

    申请/专利号BR2010PI08188

  • 申请日2010-02-04

  • 分类号C07D487/04;A61K31/5025;A61P35;C07D277/82;

  • 国家 BR

  • 入库时间 2022-08-21 14:26:42

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