Iodine–NH₄OAc mediated regioselective synthesis of 2-aroyl-3-arylimidazo[1,2-<i>a</i>]pyridines from 1,3-diaryl-prop-2-en-1-ones

Abstract

The present protocol describes an efficient, metal-free regioselective synthesis of 2-aroyl-3-arylimidazo[1,2-a]pyridines from 1,3-diaryl-prop-2-en-1-ones and 2-aminopyridine. The iodine-NH₄OAc promoted reaction offers a novel route in the synthesis of 2-aroyl-3-arylimidazo[1,2-a]pyridines. This protocol offers significant flexibility in accessing medicinally important 2-aroyl-3-arylimidazo[1,2-a]pyridines with various substitution patterns.