A mild, expedient, one-pot trifluoromethanesulfonic anhydride mediated synthesis of N-arylimidates

The direct transformation of various secondary amides into N-arylimidates via mild electrophilic amide activation with trifluoromethanesulfonic anhydride (Tf2O) in the presence of 2-chloropyridine (2-ClPyr) is described. Low-temperature amide activation followed by C–O bond formation with 2-naphthol provides the desired N-arylimidates in short overall reaction times. In contrast, reaction with oxindole proceeds via formation of a C–C bond to give 1-(1H-indol-2-yl)naphthalene-2-ol.