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阿折地平的合成工艺改进

阿折地平的合成工艺改进

ISSN:1005-0108
2010年第20卷第3期
研究论文
刘剑峰[1] 韩建奎[1] 侯桂华[2] 黄亚丽[1] 徐文方[3] LIU Jian-feng,HAN Jian-kui,HOU Gui-hua,HUANG Ya-li,XU Wen-fang

目的 改进抗高血压药物阿折地平的合成工艺。方法 以二苯甲胺和环氧氯丙烷为起始原料,经取代,酯化, 酸化,缩合等反应制得抗高血压药物阿折地平。结果与结论 目标化合物的结构经1H-NMR、质谱确证。总收率为30.88%,比文献收率提高了10.62%。改进后的方法操作简便,有利于工业化生产。

Aim To improve the synthetic procedure of azelnidipine.Methods Azelnidipine was synthesized from aminodiphenylmethane and epichlorohydrin via substitution,esterification,acidification,condensation,etc.Results and conclusion The structure of target compound was confirmed by ^1H-NMR,MS.The overall yield of the process is 30.88%.Compared with the reported method,the overall yield is 10.62% higher.This synthetic process is suitable for industrial preparation by its convenient operation.

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ISSN:1005-0108
2010年第20卷第3期
研究论文

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