Ring-enlargement and ring-opening reactions of 1,2-thiazetidin-3-one 1,1-dioxides with ammonia and primary amines as nucleophiles

Abstract

The N-benzyl- and N-alkyl-substituted 1,2-thiazetidin-3-one 1,1-dioxides 1b - d reacted readily with NH3 and primary amines via ring opening. The reaction with NH3 proceeded at -78° to room temperature yielding ring-opened adducts via nucleophilic attack of NH3 at the sulfonyl group, whereas the reactions with amines at room temperature yielded products via attack at the carbonyl group. The N-unsubstituted analogue 1a, when reacted with benzylamine in refluxing EtOH, also gave a product of ring opening via nucleophilic attack at the c Show more