摘要
目的合成急性胰腺炎用药氯谷胺。方法以谷氨酸和3,4-二氯苯甲酸为起始原料,经缩合、酐化、胺解反应合成了氯谷胺。结果及结论工艺简单,条件温和,适于大规模生产。
Objective: To synthesize loxiglumide, a novel drug for acute pancreas inflammation. Methods With glutamic acid and 3,4-dichlorobenzoic acid as starting materials, loxiglumide was synthesized by condensation, anhydrization and aminolysis reactions. Results and Conclusion This route can be simple and easy controlled, and can be used in a large scale production of loxiglumide.
出处
《食品与药品》
CAS
2013年第5期317-319,共3页
Food and Drug
关键词
氯谷胺
谷氨酸
3
4-二氯苯甲酸
loxiglumide
glutamic acid
3,4-dichlorobenzoic acid