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非布索坦的合成工艺研究
引用本文:张雷.非布索坦的合成工艺研究[J].精细化工,2013,30(10).
作者姓名:张雷
作者单位:华南理工大学生物科学与工程学院
基金项目:广东省科技厅国际合作项目
摘    要:以4-羟基苯甲腈为合成原料,经硫化、环合、甲酰化、氰化、烷基化、水解反应制得目标产物。改进后的工艺在氰化和烷基化时采用“一锅法”合成,同时考察了硫化反应中盐酸浓度,以及苯环甲酰化反应过程中时间、温度、甲烷磺酸和三氟乙酸比例对产物收率的影响。研究表明,该合成路线操作简单, 反应条件温和,不引入剧毒物质,收率可达到65.7%。

关 键 词:非布索坦  抗痛风药  黄嘌呤氧化酶  硫化  甲酰化  一锅法
收稿时间:4/8/2013 12:00:00 AM
修稿时间:2013/6/20 0:00:00

Improved Synthetic Process of Febuxostat
ZHANG Lei.Improved Synthetic Process of Febuxostat[J].Fine Chemicals,2013,30(10).
Authors:ZHANG Lei
Abstract:Febuxostat was prepared by 4-hydroxybenzonitrile via sulfuration, cyclization, formylation, cyanation, alkylation and hydrolysis. The cyanation and alkylation reaction were performed by one-pot reaction in improved process, and the key factors, such as concentration of hydrochloric acid, reaction time, temperature, the ratio of methane sulfonic acid to trifluoroacetic acid, were explored. The improved process was convenient, mild reaction condition, and the total yield was as high as 65.7%.
Keywords:febuxostat  antipodagric drug  xanthine oxidase  sulfuration  formylation  one-pot reaction
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