A highly-efficient and practical method for S-alkylation
of arylthioureas
was reported. Using tetraalkylammonium salts as alkylation reagents,
a series of 68 S-substituted aryl-isothioureas were obtained in good
to excellent yields under transition-metal-free conditions. The protocol
features simple performance, broad functional group tolerance, good
to excellent yields, and easily available starting materials, showing
potential synthetic value for the preparation of diverse biologically
or pharmaceutically active compounds.