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抗溃疡药马来酸伊索拉定的合成新方法
引用本文:孟繁浩,王立升,赵鑫. 抗溃疡药马来酸伊索拉定的合成新方法[J]. 中国药物化学杂志, 2002, 12(3): 155-156
作者姓名:孟繁浩  王立升  赵鑫
作者单位:1. 辽宁省医药工业研究院,辽宁,沈阳,110016
2. 广西大学工业测试实验中心,广西,南宁,530004
摘    要:采用新的合成路线制备新型抗溃疡药马来酸伊索拉定(isrogladine maleate),以对二氯苯为起始原料,经乙酰化、溴仿反应、氰化、环合、成盐五步反应制得目标化合物,其结构经谱图确证。该法原料价廉易得,三废污染少,总收率为31.2%,与原文献报道的收率相近。

关 键 词:抗溃疡药 马来酸伊索拉定 合成
文章编号:1005-0108(2002)03-0155-02

New synthetic method of the antiulcer drug irsogladine maleate
MENG Fan hao ,WANG Li sheng ,ZHAO Xin. New synthetic method of the antiulcer drug irsogladine maleate[J]. Chinese Journal of Medicinal Chemistry, 2002, 12(3): 155-156
Authors:MENG Fan hao   WANG Li sheng   ZHAO Xin
Affiliation:MENG Fan hao 1,WANG Li sheng 2,ZHAO Xin 1
Abstract:Irsogladine maleate as an antiulcer drug was synthesized according to a new route. p Dichlorobenzene which is more inexpensive and more easily available was used as the starting material through acetylation,bromoformation,cyanidation,cyclization and saltation steps to gain the target compound.The structure of the final compound was confirmed by IR, 1H NMR,MS and elemental analysis.The overall yield was 31 2% and it was similar to that in the former report.
Keywords:antiulcer drug  irsogladine maleate  synthesis
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