A Synthesis of Functionalized Benzimidazoles via the Three-Component Reaction of Terminal Alkynes, Phenylsulfonyl Azide, and Phenylenediamine-1,3-dicarbonyl Adducts

Abstract Functionalized benzimidazoles are produced through a three-component reaction that combines phenylenediamine-1,3-dicarbonyl adducts, terminal alkynes, and phenylsulfonyl azide. This synthesis involves the generation of N-sulfonylketenimine intermediates via a copper-catalyzed azide-alkyne cycloaddition, which is subsequently followed by cyclization with the phenylenediamine-1,3-dicarbonyl adducts. The method is noted for its efficiency and versatility across a range of substrates, with the final compound’s structure being validated through single-crystal X-ray analysis.