An efficient method for the synthesis of 2-pyridones via C–H bond functionalization

Abstract

A simple and practical method to access N-substituted 2-pyridones via a formal [3+3] annulation of enaminones with acrylates based on Rh^III-catalyzed C–H functionalization was developed. Control and deuterated experiments led to a plausible mechanism involving C–H bond cross-coupling and aminolysis cyclization. This strategy provides a short synthesis of structural motifs of N-substituted 2-pyridones.