Schneller S W, Hosmane R S, MacCartney L B, Hessinger D A
J Med Chem. 1978 Sep;21(9):990-3. doi: 10.1021/jm00207a028.
The synthesis of 1H-pyrrolo[3,2-c]pyridine-4,6(5H,7H)-dione (3,7-dideazaxanthine) (1), 5-methyl-1H-pyrrolo-[3,2-c]pyridine-4,6(5H,7H)-dione (1-methyl-3,7-dideazaxanthine) (2), and 1,7-dihydropyrano[4,3-b]pyrrole-4,6-dione (1-oxa-1,3,7-trideazaxanthine) (3) has been accomplished from 3-alkoxycarbonylpyrrole-2-acetates (4, 11, and 12 for 1 and 2) and from 3-carboxypyrrole-2-acetic acid (6 for 3). Compounds 1 and 2 have been found to be weak inhibitors of the noncompetitive type for xanthine oxidase while 3 showed no inhibitory properties toward this enzyme.
已由3 - 烷氧羰基吡咯 - 2 - 乙酸酯(1和2分别为4、11和12)以及3 - 羧基吡咯 - 2 - 乙酸(3为6)完成了1H - 吡咯并[3,2 - c]吡啶 - 4,6(5H,7H) - 二酮(3,7 - 二脱氮黄嘌呤)(1)、5 - 甲基 - 1H - 吡咯并[3,2 - c]吡啶 - 4,6(5H,7H) - 二酮(1 - 甲基 - 3,7 - 二脱氮黄嘌呤)(2)和1,7 - 二氢吡喃并[4,3 - b]吡咯 - 4,6 - 二酮(1 - 氧杂 - 1,3,7 - 三脱氮黄嘌呤)(3)的合成。已发现化合物1和2是黄嘌呤氧化酶的非竞争性弱抑制剂,而3对该酶无抑制作用。