首页> 外国专利> 4-Phenyl-piperazino-alkyl anthranilate deriv prepn. - from 2-nitro-benzoic acid via acid halide or salts, condensation with phenyl-piperazino-alkyl radical and reduction

4-Phenyl-piperazino-alkyl anthranilate deriv prepn. - from 2-nitro-benzoic acid via acid halide or salts, condensation with phenyl-piperazino-alkyl radical and reduction

机译:4-苯基哌嗪子烷基邻氨基苯甲酸酯衍生物prepn。 -由2-硝基苯甲酸经酰卤或盐类与苯基哌嗪子烷基缩合并还原

摘要

Process for the preparation of cpds. (I) using the following stages: -preparation of an acid halide of 2-nitro-benzoic acid or its alkali metal or tertiary base salts an condensation of this acid halide or salt with the substd. phenyl-piperazino-alkyl radical of (I). These reactions may be effected in one stage or in two or three successive stages. The nitro group is reduced to amino at the end of this reaction sequence or during it. where A = opt. branched 1-5C alkylene, R = halo, trihalomethyl, trihalomethoxy or trihalomethylthio. Parent patent states cpds. are analgosics. Present process gives good yields by simple methods.
机译:cpds的制备过程。 (I)使用以下步骤:-制备2-硝基-苯甲酸的酰卤或其碱金属或叔碱盐,使该酰卤或盐与缩合物缩合。 (I)的苯基-哌嗪子基-烷基。这些反应可以一个阶段或两个或三个连续阶段进行。在该反应序列的结尾或过程中,硝基被还原为氨基。其中A = opt。支链的1-5C亚烷基,R =卤素,三卤甲基,三卤甲氧基或三卤甲硫基。父专利声明了cpds。是止痛药。本方法通过简单的方法可获得良好的产率。

著录项

  • 公开/公告号FR2280634B2

    专利类型

  • 公开/公告日1977-03-18

    原文格式PDF

  • 申请/专利权人 SYNTHELABO;

    申请/专利号FR19740026545

  • 发明设计人

    申请日1974-07-31

  • 分类号C07D295/14;

  • 国家 FR

  • 入库时间 2022-08-22 23:51:28

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