首页> 外国专利> New phenylethanolamino- and phenylethanolaminomethyltetralines process for the preparation thereof inermediates in said process and pharmaceutical compositions containing them

New phenylethanolamino- and phenylethanolaminomethyltetralines process for the preparation thereof inermediates in said process and pharmaceutical compositions containing them

机译:在所述方法中中间体的新的苯乙醇氨基-和苯乙醇氨基甲基四联苯的制备方法以及包含它们的药物组合物

摘要

Phenylethanolamino- and phenylethanolaminomethyl-tetralins of formula (I) IMAGE in which X represents a hydrogen atom, a halogen atom, a (C1-C4)alkyl group or a trifluoromethyl group, A represents a bond between the group -COOR and the tetralin ring, a (C1-C4)alkylene group or a (C2-C4)alkenylene group, R is a hydrogen atom or a (C1-C4)alkyl group, and n is 0 or 1 and their salts, are prepared, for example, by reaction of an epoxide of formula (IIa) IMAGE with a tetralin of formula (III) IMAGE in which A and n are as defined above and R' is a (C1-C4)alkyl group, if appropriate followed by a basic hydrolysis to give the compounds (I) where R is hydrogen. The novel compounds have very advantageous properties as antidepressant agents and intestinal spasmolytics. The novel intermediates of formula (III) are also claimed.
机译:式(I)的苯基乙醇氨基-和苯基乙醇氨基甲基-四氢萘酚(IMAGE),其中X表示氢原子,卤素原子,(C1-C4)烷基或三氟甲基,A表示-COOR基团与-COOR之间的键。制备四氢萘环,(C1-C4)亚烷基或(C2-C4)亚烯基,R为氢原子或(C1-C4)烷基,n为0或1及其盐。例如,通过使式(IIa)的环氧化物与式(III)的四氢化萘进行反应,其中A和n如上所定义且R'为(C1-C4)烷基然后进行碱性水解,得到化合物(Ⅰ),其中R是氢。该新型化合物作为抗抑郁药和肠解痉剂具有非常有利的性能。还要求保护式(III)的新型中间体。

著录项

  • 公开/公告号IE67166B1

    专利类型

  • 公开/公告日1996-03-06

    原文格式PDF

  • 申请/专利权人 ELF SANOFI;

    申请/专利号IE19920000495

  • 申请日1992-02-17

  • 分类号C07C227/00;C07C229/34;C07C223/02;

  • 国家 IE

  • 入库时间 2022-08-22 03:53:53

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