摘要
目的改进2-巯基-5-甲氧基苯并咪唑的合成工艺。方法以对氨基苯甲醚为起始原料,采用醋酸硝酰作硝化剂进行硝化;采用雷尼镍催化加氢法进行还原。结果制得了奥美拉唑中间体2-巯基-5-甲氧基苯并咪唑,总收率78.5%。结论值得推广到工业化生产。
OBJECTIVE To improve the synthetic process of 2-Mercapto-5-Methoxybenzimidazole(1).METHODS Product(1) was synthesized from p-aminoanisole by acetylation,nitrification,hydrolysis,reduction and cyclic condensation.The nitrifying agent was nitroxyl acetate,and Ranney nickel was used as catalyst. RESULTS Totle yield was up to 78.5%.CONCLUSION It s deserved to be pushed to comercial scale production.
出处
《中国现代应用药学》
CAS
CSCD
北大核心
2006年第S1期628-629,共2页
Chinese Journal of Modern Applied Pharmacy