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Dimeric compounds of the FGF receptor agonists (FGFR), its preparation method and its application in Therapeutics

机译:FGF受体激动剂(FGFR)的二聚体化合物,其制备方法及其在治疗中的应用

摘要

Heterocyclic compounds derived from the dimerization of cellulose growth factor (or GFR) receptor. Its preparation procedure and its application in treatment. Requirement 1: agonis compound1. Among the descendant fund recipients conforming to the general formula (1): m1-l-m2 (1), M1 and M2 represent each single unit m and L equally or differently, and represent a joint liaison group connecting M1 and M2.It is characterized by that this single M-cell conforms to the general formula (2),The asterisk * indicates the link point between monomer and L-shaped can, and the link point of each 1m1 and 2M2 unit is above an R or R * alternative;R is a hydrogen atom (if the link point of L and M is above R2) or a group - CONH *;R1 represents hydrogen atom or c833318323 linear tar group; R2 represents a group - conh8322222 (if the link point of L and M is located in R) o-conh *;R3 represents a group - co8322; r8308;where R⁴ represents a hydrogen atom or a linear C₁₋₄ alkyl group; X is a halogen atom chosen from the fluorine, chlorine and bromine atoms; in the form of base or salt of addition to an acid or a base.
机译:衍生自纤维素生长因子(或GFR)受体二聚体的杂环化合物。其制备方法及其在治疗中的应用。要求1:阿戈尼斯化合物1。在符合通式(1):m1-1-m2(1)的后代资金接收者中,M1和M2分别表示m和L的单个单元,或相同或不同,表示连接M1和M2的联合联络组。其特征在于该单个M细胞符合通式(2),星号*表示单体与L形罐之间的连接点,每个1m1和2M2单元的连接点都高于R或R * ; R是氢原子(如果L和M的连接点在R2以上)或基团-CONH *; R1代表氢原子或c833318323直链焦油基团; R 2代表基团-conh8322222(如果L和M的链接点位于R中)o-conh *; R3代表基团-co8322; r8308;其中R 1代表氢原子或直链C 1-8烷基; X是选自氟,氯和溴原子的卤素原子;以碱或加成酸或碱的盐的形式存在。

著录项

  • 公开/公告号AR089452A1

    专利类型

  • 公开/公告日2014-08-27

    原文格式PDF

  • 申请/专利权人 SANOFI;

    申请/专利号AR2012P104965

  • 申请日2012-12-26

  • 分类号C07D471/04;A61K31/437;A61P3;A61P9;C07D519;

  • 国家 AR

  • 入库时间 2022-08-21 15:58:51

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