Facile construction of C , N -disulfonated 5-amino pyrazoles through an iodine-catalyzed cascade reaction.
Meiqi GengJinqiang KuangWeiwei FangMaoZhong MiaoYongmin MaPublished in: Organic & biomolecular chemistry (2022)
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.