A new procedure for the solid-phase synthesis of 2, 6-and 2, 7-diamino-4 (3H)- quinazolinones is described. The method involves coupling of 2, 4, 6-and 2, 4, 7- trichloroquinazoline to a solid support via benzyl alcohol type linkers, subsequent displacement of chlorine at C-2 then at the C-6 or C-7 positions by amines (Fig. 1) and the cleavage of the products from the resin. The palladium-catalyzed amination of C-6 and C- ...