Synthesis and properties of 4a-substituted 6,8-dimethylpyrimido-[5,5-e][1,2,4]-triazine-3,5,7-triones
作者:Yu. A. Azev、I. I. Mudretsova、E. O. Sidorov、E. L. Pidémskii、A. G. Goloneva、G. A. Aleksandrova
DOI:10.1007/bf00758763
日期:1987.7
The pyrimidotriazine antibiotics possess a wide spectrum of antimicrobial and antitumor activity [3, 5]. The need for convenient methods of synthesis and the desirability of discovering novel drugs amongst analogs of the pyrimidotriazine antibiotics have stimulated the development of the chemistry of these compounds. The most easily accessible pyrimidotriazine ant ibiotic is 2,3,5,6,7,8-hexahydro2
嘧啶并三嗪类抗生素具有广谱的抗菌和抗肿瘤活性 [3, 5]。对方便的合成方法的需求以及在嘧啶并三嗪类抗生素的类似物中发现新药物的需求刺激了这些化合物化学的发展。最容易获得的嘧啶并三嗪抗生素是 2,3,5,6,7,8-六氢2,6,8 三甲基嘧啶 [5,4-e] [1,2,4] 三嗪 ]3,5,7-三酮 (2 -methylfervenulone, MSD-92) [5, 6]。MDS-92 的化学性质实际上是未知的,尽管鉴于三嗪环中存在氧代基团,该化合物作为制备嘧啶并三嗪抗生素的新型类似物的起始材料具有潜在的兴趣。