Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5220087 | Tetrahedron | 2012 | 9 Pages |
Abstract
Efficient methods for the synthesis of aminomethylated azaindole derivatives via domino copper-catalyzed multicomponent coupling and cyclization have been developed. Using various secondary amines and aldehydes, N-substituted 3-ethynyl-4-aminopyridine was converted to substituted azaindoles in moderate to excellent yields. By use of a 3,4-diaminopyridine derivative bearing two alkynyl groups, the corresponding pyrrole-fused azaindoles were synthesized by controlled stepwise cyclization.
Graphical abstractDownload full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Zengye Hou, Yamato Suzuki, Shinya Oishi, Nobutaka Fujii, Hiroaki Ohno,