首页 | 本学科首页   官方微博 | 高级检索  
     

甲磺酸多沙唑嗪的合成
引用本文:王春风,应会荣,蒋成君.甲磺酸多沙唑嗪的合成[J].浙江化工,2009,40(2):1-3.
作者姓名:王春风  应会荣  蒋成君
作者单位:1. 浙江新东港药业股份有限公司,浙江,台州,318000
2. 浙江科技学院生物与化学工程学院,浙江,杭州,310023
摘    要:丙烯酸乙酯经溴化,与邻苯二酚环合,哌嗪化,成盐制得中间体1-(1,4-苯并二噁烷-2-甲酰基)哌嗪盐酸盐。该中间体与2-氯-4-氨基-6,7-二甲氧基喹唑啉反应制得盐酸多沙唑嗪,再与甲磺酸反应得甲磺酸多沙唑嗪,对反应溶剂进行选择,在最优溶剂条件下,总收率为29.7%,该方法工艺简单,适用于工业化生产。

关 键 词:多沙唑嗪  抗高血压药  甲磺酸

Synthesis of Dexazosin Mesylate
WANG Chun-feng,Yin Hui-rong,JIANG Cheng-jun.Synthesis of Dexazosin Mesylate[J].Zhejiang Chemical Industry,2009,40(2):1-3.
Authors:WANG Chun-feng  Yin Hui-rong  JIANG Cheng-jun
Affiliation:WANG Chun-feng ,Yin Hui-rong ,JIANG Cheng-jun (1.Zhejiang Neo-Dankong Pharmaceutical Co., Ltd., Taizhou 318000,China; 2.School of Biological and Chemical Engineering,Zhejiang University of Science and Technology, Hangzhou 310023,China)
Abstract:The intermediate (1,4-benzdioxazolyl-2-formyl)piperazine were prepared from catechol by cyclization, amination. Mesylate doxazosin was synthesized from doxazosin hydrochloride which prepared by condensing the intermediate with 2-chloro-4-amino--6,7-dimethoxyquinazoline. The yield of the product was 29.7%, and the synthetic route was easy to operate and suitable for industrialization.
Keywords:doxazosin  synthesis  catechol
本文献已被 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号