A convenient procedure for the synthesis of quinazolinimines and quinazolinamines from 2-fluorobenzonitriles has been developed. By using KOtBu as the promotor with 2-aminopyridines or amidines as the reaction partner, the desired heterocycles were produced in moderate to good yields under catalyst-free conditions.
J. Feng and X. Wu, Org. Biomol. Chem., 2015, 13, 10656 DOI: 10.1039/C5OB01587A
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