Facile construction of ,-disulfonated 5-amino pyrazoles through an iodine-catalyzed cascade reaction

A green and facile synthesis of previously unreported C , N -disulfonated 5-amino pyrazoles was established through an iodine-catalyzed cascade reaction of easily accessible sulfonyl hydrazides, β-ketonitriles, and sodium sulfinates. Diverse C , N -disulfonated 5-amino pyrazoles could be obtained in 38-88% yields. This methodology features green and mild conditions, broad substrate scope, and effortless work-up. A green and facile synthesis of previously unreported C,N -disulfonated 5-amino pyrazoles was established through an iodine-catalyzed cascade reaction.