Résumé/Abstract A parallel method for the synthesis of the title compounds is described. Thus, methyl anthranilates (5) are transformed into 2-aminobenzohydrazides (3) which were treated with 4-oxo acids (4) to afford in high yields and acceptable purity of piridazino [3, 2-b] quinazolines (1). Compounds (1) present four diversity centers (R 1, R 2, R 3, and R 4). The range of chemically acceptable substituents at each center has been evaluated. The ...