Metal-free electrochemical [3 + 2] heteroannulation of anilines with pyridines enabled by dual C-H radical aminations

An unprecedented metal-/external-oxidant-free electrochemical intermolecular [3 + 2] heteroannulation of anilines with electron-deficient pyridines enabled by dual C-H radical aminations for producing functionally diverse benzo[4,5]imidazo[1,2- a ]pyridines is described. The site-selectivity of aminations of aryl C(sp 2 )-H bonds relies on the electronic effect of two reaction partners: each contributed two reactive sites (a C(sp 2 )-H bond and a nitrogen atom-based functional group) and the electron-withdrawing groups at the 4 position of the pyridine ring are crucial. Mechanistic studies show that this method sequence consists of the generation of the nitrogen-centered radical (NCR) and the pyridine radical anion, radical coupling and dual C-N aminations. A metal-/external-oxidant-free electrochemical [3 + 2] heteroannulation of anilines and pyridines by dual C-H aminations toward benzo[4,5]imidazo[1,2- a ]pyridines is presented.