Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5278072 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
An efficient method is developed for the synthesis of imidazo[1,5-a]pyridine from the reaction of 1,1-dibromo-1-alkenes with 2-aminomethylpyridines. The reaction requires an inorganic base, such as Na2CO3, and moderate heating in DMF to proceed. Moderate to good yields are obtained. As demonstrated by the authors and others, 1,1-dibromo-1-alkenes are employed as synthons for activated carboxyl groups.
Graphical abstractA facile synthesis of imidazo[1,5-a]pyridines is described. Moderate to good yields are obtained.Download full-size image
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Aimin Zhang, Xiaoling Zheng, Junfa Fan, Wang Shen,