Preparation and some reactions of 6-arylsulphonimidobenzoxazol-2(3H)-ones
Abstract
The title compounds, prepared from 6-arylsulphonamidobenzoxazol-2(3H)-ones by oxidation, undergo addition of hydrogen chloride, hydrazoic acid, benzenesulphinic acid, and acetylacetone to give substituted benzoxazol-2(3H)-ones. In contrast, piperidine and methanol cleave the heterocyclic ring.