Długosz A, Duś D
Department of Organic Chemistry, University of Medicine, Faculty of Pharmacy, Grodzka, Poland.
Farmaco. 1996 May;51(5):367-74.
The synthesis and antitumor properties of pyrimido[4,5-b]quinolines have been described starting from 4-arylamino-5-carboxy-2-hydroxy-6-methylpyrimidines by reaction with PPA or POCl3. The reduced pyrimidoquinolines and derivatives with alkylating function have also been obtained.
从4-芳基氨基-5-羧基-2-羟基-6-甲基嘧啶出发,通过与多聚磷酸(PPA)或三氯氧磷(POCl3)反应,已对嘧啶并[4,5-b]喹啉的合成及其抗肿瘤特性进行了描述。还获得了还原型嘧啶并喹啉以及具有烷基化功能的衍生物。