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7,8-二甲氧基-3-(3-碘丙基)-1,3-二氢-2H-3-苯并氮杂革-2-酮的制备
引用本文:刘燕平,黄昕明,王德才.7,8-二甲氧基-3-(3-碘丙基)-1,3-二氢-2H-3-苯并氮杂革-2-酮的制备[J].华西药学杂志,2008,23(3).
作者姓名:刘燕平  黄昕明  王德才
作者单位:南京工业大学制药与生命科学学院,江苏,南京,210009
摘    要:目的合成抗心绞痛的新药伊伐布雷定的关键中间体7,8-二甲氧基-3-(3-碘丙基)-1,3-二氢-2H-3-苯并氮杂--2-酮。方法以3,4-二甲氧基苯乙酸为原料,经卤化、酰化、环合、烷基化、碘取代等反应制得目标化合物。结果五步反应总收率为63.6%,产物经MS1、HNMR确证结构。结论所用工艺路线具有原料易得、操作简便、收率较高的特点,适用于该中间体的放大制备。

关 键 词:7  8-二甲氧基-3-(3-碘丙基)-1  3-二氢-2H-3-苯并氮杂-2-酮  伊伐布雷定  心绞痛  中间体  制备

Preparation of 7,8-dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one
LIU Yan-ping,HUANG Xin-ming,WANG De-cai.Preparation of 7,8-dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one[J].West China Journal of Pharmaceutical Sciences,2008,23(3).
Authors:LIU Yan-ping  HUANG Xin-ming  WANG De-cai
Abstract:OBJECTIVE To synthesize 7,8-dimethoxy-3-(3-iodopropyl)-1,3-dihydro-2H-3-benzazepin-2-one,a key intermediate of Ivabradine(a new antianginal drug).METHODS The target compound was synthesized from 3,4-dimethoxyphenylacetic acid via halogenation,acylation,cyclization,alkylation and iodine substitution reaction.RESULTS Chemical structure of compounds was confirmed by MS and 1HNMR and overall yield was 63.6%.CONCLUCION The materials are available and the procedures are manipulated easily which make the route practical and suitable to be scale-up.
Keywords:7  8-dimethoxy-3-(3-iodopropyl)-1  3-dihydro-2H-3-benzazepin-2-one  Ivabradine  Preparation  Angina  Intermediate
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