Radical Fluorosulfonamidation: A Facile Access to Sulfamoyl Fluorides

Abstract

Recently, the introduction of fluorosulfonyl (‐SO2F) groups have attracted considerable research interests, as this moiety could often afford enhanced activities and new functions in the context of chemical biology and drug discovery. Herein, we report the design and synthesis of 1‐fluorosulfamoyl‐pyridinium (FSAP) salts, which could serve as an effective photoredox‐active precursor to fluorosulfamoyl radicals and enable the direct radical C−H fluorosulfonamidation of a variety of (hetero)arenes. This method features mild conditions, visible light, broad substrate scope, good group tolerance, etc., and a metal‐free protocol is also viable by using organic photocatalysts. Further, FSAP can also be applied to the radical functionalization of alkenes via 1,2‐difunctionalization, radical distal migration, tandem radical‐polar crossover reactions, etc. In addition, a formal C‐H methylamination of (hetero)arenes by combining this radical C−H fluorosulfonamidation with subsequent hydrolysis as well as product derivatization are also demonstrated.