Synthesis of 2‑Aryl-3-(organoselanyl)‑4H‑benzo[4,5]imidazo[2,1‑b][1,3]thiazines Promoted by N‑Fluorobenzenesulfonimide (NFSI)

An approach has been developed for the direct synthesis of various selenium-functionalized benzo­[4,5]­imidazo­[2,1-b]­[1,3]­thiazine derivatives via the electrophilic cyclization reaction between 2-(methylthio)-1-(3-arylprop-2-yn-1-yl)-1H-benzo­[d]­imidazoles and diorganyl diselenides promoted by N-fluorobenzenesulfonimide (NFSI). This strategy is used to construct fused heterocyclic scaffolds based on selenium-functionalized 4H-benzo­[4,5]­imidazo­[2,1-b]­[1,3]­thiazines using NFSI as a stable and nonhazardous oxidizing agent in the presence of CH3CN at 80 °C. The protocol allowed a broad substrate scope leading to the synthesis of 16 novel selenium-functionalized benzo­[4,5]­imidazo­[2,1-b]­[1,3]­thiazines in yields of up to 95%. Furthermore, control studies, including 1H, 19F, and 77Se NMR experiments, were conducted to identify intermediates, which contributed to the elucidation of the reaction mechanism.