Synthesis of 2-anilinobenzimidates, anthranilamides, and 2,3-dihydroquinazolin-4(1H)-ones from N-heterocyclic carbenes of indazole

N-Heterocyclic carbenes of indazole (indazol-3-ylidenes), which are substituted at Ni with aromatics were generated in situ from the corresponding indazolium salts. At 60 degrees C the indazol-3-ylidenes underwent a ring-opening under N-N bond cleavage to intermediary N-(6-methylenecyclohexa-2,4-dien-1-ylidene)anilines. Trapping of these intermediates by alcohols proved to be a convenient method for the preparation of 2-anilinobenzimidates, which have scarcely been described in the literature. The reaction temperature avoids carbene dimerization, which occurs at -80 degrees C or rearrangement of the ring-opened intermediate to acridines, which affords 100 degrees C. Water converted the ring-opened products into anthranilamides, which were cyclized on reaction with formaldehyde to 2,3-dihydroquinazolin-4(1H)-ones. (C) 2014 Elsevier Ltd. All rights reserved.