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马来酸氨氯地平的合成研究 被引量:1

Synthesis of Amlodipine Maleate
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摘要 以4-[2-(2,5-二甲基吡咯-1-基)乙氧基]乙酰乙酸乙酯、3-氨基丁烯酸甲酯和2-氯苯甲醛为起始原料,经Hantzsch成环、水解、成盐合成目标产物,总收率为53.7%。化合物经IR、1H-NMR、MS等确证。该方法具有原料易得、操作简便、收率较高、易于工业化生产等优点。 AmLodipine maleate was synthesized from ethyl 4- (2- (2, 5-dimethyl- 1H-pyrrol- 1-yl)ethoxy)-3-oxobutanoate, methyl 3-aminocrotonate and 2-chlorobenzaldehyde via Hantzsch reaction hydrolysis salification. The total yield was 53.7%. The structure of amlodipine was identified by IR, IH-NMR and MS. This method has several advantages of cheap reagents, facile reaction conditions, convenient operation and high yield.
出处 《安徽化工》 CAS 2013年第3期23-24,共2页 Anhui Chemical Industry
基金 合肥学院2012年大学生科技创新课题(11XSKY01)
关键词 马来酸氨氯地平 二氢吡啶 钙离子拮抗剂 化学合成 Amlodipine maleate Dihydropyridine Calciumion antagonist Chemical synthesis
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