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病毒唑的合成新工艺
引用本文:杨宝东,张宏森. 病毒唑的合成新工艺[J]. 黑龙江医药, 2004, 17(2): 122-123
作者姓名:杨宝东  张宏森
作者单位:哈药集团制药总厂,150086;哈药集团制药总厂,150086
摘    要:目的:采用合成新工艺提高病毒唑的收率。方法:用肌苷为原料,经乙酰化后在双磷酸酯的作用下与1,2,4-三氮唑-3-羧酸甲酯缩合,再经氨解制得产品。结果:以肌苷计,总收率为48%。结论:该合成路线简单实用,易在生产中推广。

关 键 词:病毒唑  肌苷  四乙酰核糖
修稿时间:2003-11-03

A New Sythesis of Ribavirin
Yang Baodong Harbin Pharmaceutical Factory. A New Sythesis of Ribavirin[J]. Heilongjiang Medicine, 2004, 17(2): 122-123
Authors:Yang Baodong Harbin Pharmaceutical Factory
Abstract:Objective:Using the new sythesis of Ribavirin to improve the yield.Method:Ino- sine was acetylated to tetracetylribofuranose,which was condensed with Me 1,2,4-trazole-3-car- boxylate b the aiding of bisphosphate.Then treated with NH_3 to give Ribavirin.Result:The over- all yield was 48% on the basis of inosine.Conclusion:This new synthesis route is simple and use- ful,can be easily realized in the wide production.
Keywords:Ribavirin  Inosine  Tetracetylrihofuranose
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