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2-巯基-5-甲氧基-1H-苯并咪唑的合成工艺的改进
引用本文:张艳莲.2-巯基-5-甲氧基-1H-苯并咪唑的合成工艺的改进[J].辽宁医学院学报,2004,25(3):44-45.
作者姓名:张艳莲
作者单位:锦州九泰药业有限责任公司,辽宁,锦州,121012
摘    要:目的 对2-巯基-5-甲氧基-1H-苯并咪唑的合成工艺进行改进。方法 以对氨基苯甲醚为原料,经氨基保护后硝化得2-硝基-4-甲氧基乙酰苯胺,然后酰胺基水解得2-硝基-4-甲氧基苯胺,再将硝基还原为氨基得4-甲氧基-1,2-苯二胺,最后环合得2-巯基-5-甲氧基-1H-苯并咪唑。结果 此法得到的2-巯基-5-甲氧基-1H-苯并咪唑质量、收率高,成本低。结论 此法简化了操作,适于工业化生产。

关 键 词:2-巯基-5-甲氧基-1H-苯并咪唑  合成  改进  中间体  质子泵抑制剂  奥美拉唑
文章编号:1000-5161(2004)03-0044-02
修稿时间:2004年3月3日

Improvement on Synthetic Technology of 2-mercatto-5-methoxy-1H-benzimidazole
ZHANG Yan-lian.Improvement on Synthetic Technology of 2-mercatto-5-methoxy-1H-benzimidazole[J].Journal of Liaoning Medical University (LNMU) Bimonthly,2004,25(3):44-45.
Authors:ZHANG Yan-lian
Abstract:Objective The improve the synthetic technology of 2-mercatto-5-methoxy-1H-benzimidazole. Methods The improvement was carried out in synthesizing the 2-roercatto-5-methoxy-1H-benzimidazole. The target from paminocanisole by protecting the amino-group first,then nitrofying,hydrolysizing aeylamide,reducting nitryl and cyclizating. Results The reaction method improved made the quality better,the yield higher and the cost lower. Conclusions The method was simple and convenient for synthesizing 2-mercatto-5-methoxy-1H-benzimidazole,and so the process was feasible in industry.
Keywords:synthesis  2-Mercatto-5-methoxy-1H-Benzimidazde  intermediate  inhibitor for proton pump  omeprazole
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