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西尼地平的合成工艺研究

Study on the Synthesis Technology of Cilnidipine
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摘要 以乙酰乙酸甲氧基乙基酯、乙酰乙酸肉桂醇酯为起始原料,经中间体3-氨基巴豆酸肉桂醇酯,通过Aldol缩合、Hantzsch环合反应,合成出了钙离子拮抗剂西尼地平。该合成工艺安全可行,操作简单,适合工业化生产。 With 2-methoxyethyl acetoacetate and cinnamyl acetoacetate as the starting materials, the cilnidipine can be obtained from 3-Aminocrotonic Cinnamate by Aldol condensation and Hantzsch cyclization. It is a suitable way to produce cilnidipin industrially,which provides the advantage of simplicity and safety.
出处 《安徽化工》 CAS 2014年第5期33-34,共2页 Anhui Chemical Industry
关键词 西尼地平 钙拮抗剂 合成 cilnidipine dihydropyridine calcium antagonist synthesis
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  • 1恽榴红,冯茜.去甲麦普替林的合成[J].中国医药工业杂志,1989,20(2):53-54. 被引量:2
  • 2陈新,高亚平,黄文龙,郭晓东.钙拮抗剂尼莫地平的合成[J].中国医药工业杂志,1989,20(2):52-53. 被引量:13
  • 3武引文,颜廷仁,聂辉,袁凤燕.间尼索地平的合成[J].中国医药工业杂志,1989,20(3):104-106. 被引量:6
  • 4Mealy N. ,Castaner J. ,Cilnidipine [J]. Drugs Future, 1996, 21 (3) : 249-253.
  • 5Fujil S.,Kameyama K.,Husone M. et al. Effect ofeilnidipine, anovel dihydro pyridine Ca^2+ channel antagonist, on N-type Ca^2+ channel in rat dorsal root ganglion neurons [J]. Pharmacol. Exp. Ther., 1997,280(3 ) : 1184.
  • 6Kutsuma T.,lkawa H, Sato Y. 1,4-Dihydropyridine derivatives and pharmaceutical compositions comprising them [P]. EP: 161877,1986.
  • 7Takeda S.,Urdhiba H.,Hattori Y.,et al. Cilnidipine,the N- and L-type ealeium channel antagonist, reduced on 24-hurinary catescholam-ines and c-peptide in hypertensive [J]. Pharmacotherapy, 2000,20( 7 ) : 819-822.
  • 8Mealy N, Castaner J. Cilnidipine [J]. Drugs Future,1996, 21(3) : 249-253.
  • 9Kutsuma T, Ikawa H, Sato Y. 1,4-Dihydropyridine derivatives and pharmaceutical compositions comprising them [P]. EP: 161877, 1985-11-21. (CA 1986,104: 207168x)
  • 10陈芬儿.有机药物合成法[M].上海:中国医药科技出版社,1999.310.

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