Transformations of 3-aryl-2-chloro-2-imidoylaziridines: Novel entries to 4-chloro-2,5-diaryl-1H-imidazoles and 2-chloro-2-acylaziridines

摘要

The reactivity of stereochemically defined 3-aryl-2-chloro-2- imidoylaziridines, an unexplored class of substituted aziridines, was investigated under various reaction conditions. 2-Chloro-2-imidoylaziridines underwent a novel thermal rearrangement by reflux in acetonitrile via C-C bond cleavage to 4-chloro-2,5-diarylimidazoles in high yield. Alternatively, a novel efficient entry toward 2-aroyl-2-chloroaziridines was based on the chemoselective hydrolysis of 2-chloro-2-imidoylaziridines with hydrochloric acid in aqueous tetrahydrofuran.