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Process for preparation of bevantolol hydrochloride

机译:盐酸贝伐洛尔的制备方法

摘要

Disclosed is a new process for preparing bevantolol hydrochloride suitable for industrial production in which bevantolol hydrochloride can be obtained in a high yield and HVA of an expensive material can be recovered. The process for the preparation of bevantolol hydrochloride comprises the steps of: causing 3-(m-tolyloxy)-1,2- epoxypropane (TOEP) to react with &bgr;-(3,4-dimethoxyphenyl)ethylamine (HVA) of excess mole per mole of said TOEP; dissolving the reaction mixture in a halogenated hydrocarbon to give a solution; mixing the solution with hydrochloric acid; separating an organic layer from the resulting mixture; and obtaining 1-[(3,4-dimethoxyphenethyl)amino]-3-(m- tolyloxy)-2-propanol hydrochloride from the organic layer.
机译:公开了一种制备适于工业生产的盐酸贝伐洛尔的新方法,其中可以高收率获得盐酸贝伐洛尔,并且可以回收昂贵材料的HVA。盐酸贝伐洛尔的制备方法包括以下步骤:使3-(间甲苯基)-1,2-环氧丙烷(TOEP)与过量摩尔的-(3,4-二甲氧基苯基)乙胺(HVA)反应每摩尔所说的TOEP;将反应混合物溶解在卤代烃中得到溶液。将溶液与盐酸混合;从所得混合物中分离出有机层;从有机层中获得1-[((3,4-二甲氧基苯乙基)氨基] -3-(间甲苯氧基)-2-丙醇盐酸盐。

著录项

  • 公开/公告号US5382689A

    专利类型

  • 公开/公告日1995-01-17

    原文格式PDF

  • 申请/专利权人 NIPPON CHEMIPHAR CO. LTD.;

    申请/专利号US19920955328

  • 发明设计人 YUTAKA NOMURA;

    申请日1992-10-01

  • 分类号C07C209/16;

  • 国家 US

  • 入库时间 2022-08-22 04:05:35

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