Discovery and hit-to-lead optimization of non-ATP competitive MK2 (MAPKAPK2) inhibitors
Abstract
Bulky, electron-rich phosphine ligands with a biphenyl backbone, when combined with Pd(OAc)2, give highly active catalysts for the α-arylation of ketones. The ligand 2-methyl-2'-dicyclohexylphosphinobiphenyl is particularly effective, and with 0.1-1.0 mol % Pd, a large variety of aryl halides and ketones react efficiently and with high selectivity. For two types of substrates, the ligands BINAP and Xantphos are more effective than the biphenyl-based ligands. It is also shown that K3PO4 can be used as the base in these reactions, and that base-sensitive functional groups are better tolerated if this is used instead of NaO(t)Bu or NaHMDS. In some cases, α- aryl ketones can be produced without adding a ligand to the reaction. Although the substrate scope of the ligandless conditions is limited, some combinations react in high yield, and in one case, 100 000 turnovers were obtained. The results of experiments on the Pd-catalyzed arylation of diethyl malonate, cyclic 1,3-diketones, and nitroalkanes are also reported.
Publication Title
ACS Medicinal Chemistry Letters
Recommended Citation
Fox, J., Huang, X., Chieffi, A., & Buchwald, S. (2011). Discovery and hit-to-lead optimization of non-ATP competitive MK2 (MAPKAPK2) inhibitors. ACS Medicinal Chemistry Letters, 2 (8), 632-637. https://doi.org/10.1021/ml200113y
