A series of the title compounds was prepared via condensation of the 3-(aminomethyl) triazolylbenzophenone (5) with N-protected amino acids, followed by deprotection, amination of the 3-[(chloroacetamido) methyl] triazolyl-benzophenone (6a, b), or reduction of the relevant azide derivative (6c). Some of the title compounds were also derived directly from the quinazolines 3 or 4 by acid-induced rearrangement, followed by deprotection. ...