Botros S, Khalifa M
Pharmazie. 1976;31(3):155-7.
The preparation of certain 3-substituted derivatives of 3.4-dihydro-2-methyl-4-oxoquinazoline is described. The synthesis fo a quinazolone-barbituric acid derivative, in which the two constituting moieties are separated by methylene groups, was achieved by reacting 3-[B-haloethyl]-3.4-dihydro-2-methyl-4-oxoquinazoline with sodio malonic ester and subsequent cyclization of the ester so formed with urea. Attempts to introduce the alpha-glutaryl group at the position 3 of the quinazolone ring system via different routes were unsuccessful.
描述了某些3,4-二氢-2-甲基-4-氧代喹唑啉的3-取代衍生物的制备。通过使3-[β-卤代乙基]-3,4-二氢-2-甲基-4-氧代喹唑啉与丙二酸二钠反应,然后将如此形成的酯与尿素环化,实现了喹唑酮-巴比妥酸衍生物的合成,其中两个组成部分由亚甲基隔开。试图通过不同途径在喹唑酮环系统的3位引入α-戊二酰基的尝试均未成功。