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New intermediate for the preparation of amlodipine besylate and its process

机译:苯磺酸氨氯地平的制备新中间体及其工艺

摘要

PURPOSE: Provided are a novel intermediate for the preparation of amlodipine besylate and its process, which intermediate contains triazole group and used as a starting material in synthesizing amlodipine besylate environment friendly. CONSTITUTION: Triazone derivatives of the formula(5) is manufactured by the steps of: reacting ethanol amine and 1,3-dimethylhexahydro-2-oxo-1,3,5-triazine derivative to prepare a compound of the formula(6); introducing ketoester group thereinto to prepare a compound of the formula(7); reacting the compound of the formula(7) with 2-chlorobenzaldehyde in the presence of low alcoholic reaction solvent and followed by refluxing and neutralizing it; reacting resultant solution with methyl-3-aminochlotonate to obtain triazone compound of the formula(5).
机译:目的:提供一种新型的中间体,用于制备苯磺酸氨氯地平及其中间体,该中间体含有三唑基,是合成环保型苯磺酸氨氯地平的起始原料。组成:式(5)的三氮唑衍生物是通过以下步骤制备的:将乙醇胺与1,3-二甲基六氢-2-氧代-1,3,5-三嗪衍生物反应以制备式(6)的化合物;向其中引入酮酯基以制备式(7)的化合物;使式(7)化合物与2-氯苯甲醛在低醇反应溶剂的存在下反应,然后回流并中和。使所得溶液与-3-氨基氯代甲酯反应,得到式(5)的三氮唑化合物。

著录项

  • 公开/公告号KR20020000077A

    专利类型

  • 公开/公告日2002-01-04

    原文格式PDF

  • 申请/专利权人 KOREA UNITED PHARM. INC.;

    申请/专利号KR20000034178

  • 发明设计人 AHN SEUNG HO;CHO YUN HWAN;

    申请日2000-06-21

  • 分类号C07D401/12;

  • 国家 KR

  • 入库时间 2022-08-22 00:31:49

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