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盐酸帕洛诺司琼中间体的合成
引用本文:王平,陶春妙.盐酸帕洛诺司琼中间体的合成[J].浙江化工,2009,40(9):13-15.
作者姓名:王平  陶春妙
作者单位:浙江工业大学药学院,浙江,杭州,310014
摘    要:研究了双(三氯甲基)碳酸酯替代传统氯代试剂合成盐酸帕洛诺司琼中间体的新工艺路线。以1-萘甲酸为起始原料,经还原,氯化,酰胺化,手性拆分,得到盐酸帕洛诺司琼中间体,该工艺具有生产安全,环境友好,操作简单等优点,反应总收率为26.8%。

关 键 词:盐酸帕洛诺司琼  双(三氯甲基)碳酸酯  合成

Synthesis of the Chemical Intermediate of Palonosetron Hydrochloride
WANG Ping,TAO Chun-miao.Synthesis of the Chemical Intermediate of Palonosetron Hydrochloride[J].Zhejiang Chemical Industry,2009,40(9):13-15.
Authors:WANG Ping  TAO Chun-miao
Affiliation:(College of Pharmaceutical Sciences, Zhejiang University of Technology, Hangzhou, 310014, China)
Abstract:The bis(trichloromethyl)carbonate replaced the traditional chlorination reagent to synthesize of the chemical intermediate of palonosetron hydrochloride. The chemical intermediate of palonosetron hydrochloride was synthesized from α-naphthoic acid via reduction, chlorination, amidation and chiral resolution. The advantages of this procedure are simple, safe and environmentally friendly. The total yield was 26.8%。
Keywords:palonosetron hydrochloride  bis-trichloromethyl carbonate  synthesis
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