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Method for the synthesis of pharmacologically active compounds and intermediates for such synthesis

机译:合成药理活性化合物的方法和用于该合成的中间体

摘要

A process for the preparation of an aryloxypropanolamine of the formula ##EQU1## wherein Ar is a carbocyclic or heterocyclic aromatic group and R is an alkyl or substituted alkyl group having 1 to 6 carbon atoms, characterized in subjecting a compound of the formula ##STR1## to oxidative cleavage to a dialdehyde of the formula ##STR2## which is then made subject to reduction, amination, acetal hydrolysis, and, where required, removal of a nitrogen protective group, to the formation of a compound of formula I, or an acid addition salt thereof, a compound of formula II and the preparation thereof from mannitol.
机译:制备式## EQU1 ##的芳氧基丙醇胺的方法,其中Ar是碳环或杂环芳族基团,R是具有1-6个碳原子的烷基或取代的烷基,其特征在于,使式#化合物#STR1 ##氧化裂解为式## STR2 ##的二醛,然后使其还原,胺化,乙缩醛水解,并在需要时除去氮保护基,从而形成式I或其酸加成盐,式II化合物及其由甘露醇制备。

著录项

  • 公开/公告号US4777293A

    专利类型

  • 公开/公告日1988-10-11

    原文格式PDF

  • 申请/专利权人 AKTIEBOLAGET HASSLE;

    申请/专利号US19850753682

  • 发明设计人 BO R. LAMM;

    申请日1985-07-10

  • 分类号C07C93/06;C07D209/04;C07D417/04;

  • 国家 US

  • 入库时间 2022-08-22 06:48:30

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