Facile construction of C , N -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...

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Veröffentlicht in:Organic & biomolecular chemistry 2022-11, Vol.20 (42), p.8187-8191
Hauptverfasser: Geng, Meiqi, Kuang, Jinqiang, Fang, Weiwei, Miao, Maozhong, Ma, Yongmin
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Sprache:eng
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Zusammenfassung: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.
ISSN:1477-0520
1477-0539
DOI:10.1039/d2ob01647h