Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5218697 | Tetrahedron | 2012 | 7 Pages |
Abstract
A facile and efficient one-pot synthesis of 1,4-disubstituted 3-amino-2-pyridone derivatives via three-component reactions of readily available alkynyl aldehydes, amines, and ethyl 2-((diphenylmethylene)amino)acetate has been developed. The alkynyl aldehyde substrates and the amine partners can be flexibly varied to achieve a range of 3-amino-2-pyridone derivatives, which could exert interesting chemical and biological properties. The reaction mechanism for the formation of 3-amino-2-pyridone derivatives is briefly explained.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Qingfa Zhou, Xueping Chu, Weifang Tang, Tao Lu,