Solvent-Free Buchwald-Hartwig Amination of Heteroaryl Chlorides by N -Heterocyclic Carbene-Palladium Complex (SIPr) Ph2 Pd(cin)Cl at Room Temperature.
Jia-Sheng OuyangXinhuan ZhangBendu PanHaobin ZouAlbert Sun-Chi ChanLiqin QiuPublished in: Organic letters (2023)
Using the robust N -heterocyclic carbene-palladium complex (SIPr) Ph2 Pd(cin)Cl, a highly efficient and easy-to-operate method has been developed at room temperature for the solvent-free Buchwald-Hartwig amination of heteroaryl chlorides with various amines. The amount of catalyst can be as low as 0.05 wt %. The system was demonstrated on 47 substrates and successfully applied to the synthesis of commercial pharmaceuticals and candidate drugs with high yields. Furthermore, the protocol can be used to prepare aniline derivatives on a multigram scale without yield loss.