Sulfonimidamides by Sequential Mechanochemical Chlorinations and Aminations of Sulfinamides
Steven Terhorst, Tim Jansen, Tim Langletz, Carsten Bolm
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