首页> 外国专利> Preparation method of quinapril hydrochloride by reaction between a 2.5 - - oxazolidin and an ester of a terbutilico Tetrahydro Isoquinoline,Useful as active Principle for the treatment of hypertension and congestive heart failure

Preparation method of quinapril hydrochloride by reaction between a 2.5 - - oxazolidin and an ester of a terbutilico Tetrahydro Isoquinoline,Useful as active Principle for the treatment of hypertension and congestive heart failure

机译:2.5--恶唑烷[与叔丁基四氢异喹啉的酯反应制得盐酸奎那普的方法,用作治疗高血压和充血性心力衰竭的有效成分

摘要

Methods and materials for preparing quinapril, its pharmaceutically acceptable salts, including quinapril hydrochloride, are disclosed. The method includes reacting (2S,4S)-2-(4-methyl-2,5-dioxo-oxazolidin-3-yl)-4-phenyl-butyric acid ethyl ester with (3S)-1,2,3,4-tetrahydro-isoquinoline-3-carboxylic acid tert-butyl ester to yield quinapril tert-butyl ester, which is subsequently reacted with an acid to yield quinapril or an acid addition salt of quinapril.
机译:公开了用于制备喹那普利及其药学上可接受的盐,包括盐酸喹那普利的方法和材料。该方法包括使(2S,4S)-2-(4-甲基-2,5-二氧-恶唑烷-3-基)-4-苯基丁酸乙酯与(3S)-1,2,3,4反应-四氢-异喹啉-3-羧酸叔丁酯得到奎那普叔丁酯,其随后与酸反应得到奎那普利或奎那普利的酸加成盐。

著录项

  • 公开/公告号CL2004000541A1

    专利类型

  • 公开/公告日2005-02-04

    原文格式PDF

  • 申请/专利权人 WARNER-LAMBERT COMPANY LLC;

    申请/专利号CL20040000541

  • 发明设计人 SANDRA MARIE JENNINGS;

    申请日2004-03-16

  • 分类号A61K31/47;C07D217/26;

  • 国家 CL

  • 入库时间 2022-08-21 22:18:22

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