首页> 外国专利> INTERMEDIATES FOR SYNTHESIZING TREPROSTINIL AND PREPARATION METHOD THEREOF AS WELL AS THE PREPARATION METHOD OF TREPROSTINIL THEREBY

INTERMEDIATES FOR SYNTHESIZING TREPROSTINIL AND PREPARATION METHOD THEREOF AS WELL AS THE PREPARATION METHOD OF TREPROSTINIL THEREBY

机译:合成白藜芦醇的中间体及其制备方法以及由此制备的白藜芦醇的制备方法

摘要

The present invention relates to the preparation of intermediates of treprostinil, a preparation method for same, and the preparation of treprostinil thereby. Specifically, the invention relates to the compound of formula (VI), the preparation thereof and the application of said compound for the synthesis of treprostinil (as represented by formula (I)). The method for the preparation of treprostinil comprises: obtaining the compound of formula (III) by means of reducing the compound of formula (VI) and deprotecting the hydroxy group thereof; reacting said compound of formula (III) with chloroacetonitrile followed by hydrolysis to obtain the treprostinil of formula (I). The present method is simple, yields high rates of synthesis, and is suitable for industrial production.
机译:本发明涉及曲前列环素的中间体的制备,其制备方法以及曲前列环素的制备。具体地,本发明涉及式(VI)的化合物,其制备以及所述化合物在曲前列环素(如式(I)所示)的合成中的应用。曲前列环素的制备方法包括:通过还原式(VI)的化合物并对其羟基进行脱保护得到式(III)的化合物;使所述式(III)的化合物与氯乙腈反应,然后水解,得到式(I)的曲前列环素。本发明方法简单,合成率高,适合工业化生产。

著录项

  • 公开/公告号WO2014094511A1

    专利类型

  • 公开/公告日2014-06-26

    原文格式PDF

  • 申请/专利权人 UNITRIS BIOPHARMA CO. LTD;

    申请/专利号WO2013CN87083

  • 发明设计人 ZHANG FUYAO;GUO PENGFEI;JI WEI;

    申请日2013-11-13

  • 分类号C07D309/12;C07F7/08;C07F7/18;C07C51/08;C07C59/72;

  • 国家 WO

  • 入库时间 2022-08-21 15:49:02

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