4a-甲基-4aH-吡啶并[1,2-a]喹啉-1,2,3,4-四甲酸甲酯的合成  

Synthesis of Tetramethyl 4a-methyl-4aH-pyrido[1,2-a] quinoline-1,2,3,4-tetracarboxylate

作　　者：徐雪梅[1] XU Xuemei(College of Chemical Engineering,Anhui University of Science and Technology,Huainan 232001,China)

机构地区：[1]安徽理工大学化学工程学院,安徽淮南232001

出　　处：《安阳师范学院学报》2018年第5期24-27,共4页Journal of Anyang Normal University

摘　　要：以2-甲基喹啉和丁炔二酸二甲酯为原料,经环化反应合成得到4a-甲基-4aH-吡啶并[1,2-a]喹啉-1,2,3,4-四甲酸甲酯。实验表明,无需催化剂,物料配比n(2-甲基喹啉):n(丁炔二酸二甲酯)=1:2,在二甲亚砜溶液中室温反应24小时,产物收率可达72%。目标化合物的结构得到1H NMR、13C NMR和MS证实。4a-Methyl-4aH-pyrido[1,2-a]quinoline-1,2,3,4-tetracarboxylate was synthesized by cyclization reaction from the starting materials of2-methylquinoline and dimethyl acetylenedicarboxylate.The experiments showed that72%yield were obtained under conditions of catalyst free,molar ratio of2-methylquinoline to dimethyl acetylenedicarboxylate of1:2,reaction dissolvent of DMSO,room temperature and reaction time of24h.The structure of the title compound was confirmed by1H NMR,13C NMR and MS.

关 键 词：2-甲基喹啉 丁炔二酸二甲酯 吡啶并[1 2-a]喹啉 合成 

分 类 号：O626.1[理学—有机化学] O662.6[理学—化学]