Copper-Catalyzed Annulation of Electrophilic Benzannulated Heterocycles with 2-Aminopyridine and 2-Aminoquinoline: Direct Access toward Polyring-Fused Imidazo[1,2-<i>a</i>]pyridines
Sheba Ann Babu, Varsha P. V, Susanna Poulose, Sunil Varughese, Jubi John
Abstract
We have developed a direct method for the synthesis of polyring-fused imidazo[1,2- a ]pyridines via a copper-catalyzed annulation of electrophilic benzannulated heterocycles with 2-aminopyridine and 2-aminoquinoline. From 3-nitroindoles and 2-aminopyridine, we could synthesize tetracenes, viz., indole-fused imidazo[1,2- a ]pyridines, and by starting from 2-aminoquinoline, we could generate pentacenes, viz., indolo-imidazo[1,2- a ]quinolines. In addition, we could also extend the methodology toward the synthesis of benzothieno-imidazo[1,2- a ]pyridines starting from 3-nitrobenzothiophene. Furthermore, the basic photophysical properties of these synthesized heteroacenes were evaluated.