首页> 外国专利> Processes for preparing a perindopril salt, perindopril t-butylamine, a pharmaceutically acceptable salt perindopril monohydrate, products obtained and their use

Processes for preparing a perindopril salt, perindopril t-butylamine, a pharmaceutically acceptable salt perindopril monohydrate, products obtained and their use

机译:培哚普利盐,培哚普利叔丁胺,药学上可接受的盐培哚普利一水合物的制备方法,所得产品及其用途

摘要

"PROCESSES FOR PREPARING PERINDOPRIL SALT, PERINDOPRIL T-BUTYLAMINE, A PHARMACEUTICALLY ACCEPTABLE SALT PERINDOPRIL, PRODUCTS OBTAINED AND THEIR USE". A process for preparing a pharmaceutically acceptable perindopril salt of formula (I) from a protected precursor compound of formula (II) wherein R represents a carboxyl protecting group. The process according to the invention comprises subjecting a compound of formula (II) to deprotection of the COOR carboxylic group attached to the heterocyclic ring to produce the corresponding free acid, which deprotection being performed in the presence of a base which forms a pharmaceutically salt. acceptable with said free acid formed by said deprotection. Also described is the preparation of a pharmaceutically acceptable perindopril salt monohydrate in addition to its use.
机译:“制备培哚普利盐,培哚普利T-丁二胺,药学上可接受的盐培哚普利,所获得的产品及其使用的过程”。由受保护的式(II)的前体化合物制备式(I)的药学上可接受的培哚普利盐的方法,其中R代表羧基保护基。根据本发明的方法包括使式(II)的化合物对与杂环连接的COOR羧基进行脱保护以产生相应的游离酸,该脱保护在形成药学上的盐的碱的存在下进行。通过所述脱保护形成的所述游离酸可接受。除其用途外,还描述了药学上可接受的培哚普利盐一水合物的制备。

著录项

  • 公开/公告号BR0315703A

    专利类型

  • 公开/公告日2005-10-25

    原文格式PDF

  • 申请/专利权人 CIPLA LIMITED;

    申请/专利号BR20030315703

  • 申请日2003-11-18

  • 分类号C07K5/062;A61K38/05;A61P9/00;

  • 国家 BR

  • 入库时间 2022-08-21 22:18:32

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