Synthesis of Functionalized Pyridines via a Regioselective Oxazoline Promoted C–H Amidation Reaction

The first Rh-catalyzed C–H amidation of pyridines is reported. The incorporation of a substituent at the C2 position both is crucial to the success of this transformation and provides considerable scope for further elaboration of the resulting products. Among these compounds, 2-chloropyridines allow access to a selection of intermediates including a versatile azaquinazoline scaffold.