Litcius/Paper detail

Sulfonimidamides by Sequential Mechanochemical Chlorinations and Aminations of Sulfinamides

Steven Terhorst, Tim Jansen, Tim Langletz, Carsten Bolm

2022Organic Letters29 citationsDOI

Abstract

Here, we report the first mechanochemical synthesis of sulfonimidamides. The one-pot, two-step method requires neither a solvent nor inert conditions. In a mixer mill, sulfinamides are rapidly converted to sulfonimidoyl chlorides by oxidative chlorination with N-chlorosuccinimide (NCS). Subsequent substitutions with amines provides a wide range of diversely substituted sulfonimidamides.

Topics & Concepts

ChemistryInertSolventCombinatorial chemistryHalogenationOrganic chemistrySynthesis and Catalytic ReactionsCatalytic C–H Functionalization MethodsPhenothiazines and Benzothiazines Synthesis and Activities