Login / Signup

Easy S-Alkylation of Arylthioureas and 2-Mercaptobenzothiazoles Using Tetraalkylammonium Salts under Transition-Metal-Free Conditions.

Xiao-Hu XuEr-Jun HaoZhen ShiZhi-Bing Dong
Published in: The Journal of organic chemistry (2022)
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.
Keyphrases
  • highly efficient
  • ionic liquid
  • randomized controlled trial
  • molecular docking
  • molecularly imprinted
  • human health
  • mass spectrometry
  • liquid chromatography