2-Fluoro substituted benzoyl chlorides undergo cyclocondensation with 2-amino-N- heterocycles to form 4 (3H)-quinazolinones. The reaction proceeds in moderate yields with different combinations of benzoyl chlorides and 2-amino-N-heterocycles. The products generally precipitate from the reaction mixture and require no further purification. Two tetrafluoro quinazolinones were found to be moderately active against a number of tumor ...