马来酰亚胺
环氧乙烷
化学
胺气处理
有机化学
组合化学
作者
Lu Yin,Meitian Fu,Sihan Zhao,Qiong Wu,Ruize Jiang,Chao Huang
标识
DOI:10.1021/acs.joc.5c01519
摘要
Maleimide-modified drug molecules can improve the stability and selective release of drugs. This study developed an easy-to-operate, mild, and safe synthetic drug-molecule modification strategy. This strategy employs the easily substituted characteristics of the substrate aminomaleimide and various amine-containing molecules under catalyst-free conditions. This method is suitable for various types of primary amines and secondary amines. When reacting with N-methylbenzylamine, benzo[1,4]oxazepane derivatives can be obtained by temperature adjustment. At the same time, the method has good tolerance for substrate functional groups, and 7 maleimide-modified drug molecular fragments were obtained in high yield (80-85%). This article has confirmed that the drug molecules modified by this method still have active reaction sites and can be further modified.
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