Boers F, Lemiere G, Lepoivre J A, De Groot A, Dommisse R, De Bruyne T, Vlietinck A J, Vanden Berghe D A
Department of Chemistry, University of Antwerp (RUCA), Belgium.
Pharmazie. 1998 Aug;53(8):512-7.
3',4'-Di-O-benzyl-3-O-methylquercetin (2), the precursor in the synthesis of an important antivirally active flavone 3-O-methylquercetin (1), was regioselectively alkylated at the 7-OH position by a series of 1,omega-dihaloalkanes and omega-bromoalkanols. Dimerization of the flavone had to be avoided by applying strict reaction conditions. Subsequent debenzylation was carried out by catalytic transfer hydrogenolysis, affording quantitatively the 7-O-(omega-haloalkyl)-3-O-methylquercetin (11-14) and 7-O-(omega-hydroxyalkyl)-3-O-methylquercetin derivatives (15, 16). All compounds were tested for their antiviral activity against poliomyelitis- and HIV-viruses.
3',4'-二-O-苄基-3-O-甲基槲皮素(2)是合成重要的具有抗病毒活性的黄酮3-O-甲基槲皮素(1)的前体,它在7-OH位置被一系列1,ω-二卤代烷和ω-溴代烷醇区域选择性烷基化。必须通过严格的反应条件避免黄酮的二聚化。随后通过催化转移氢解进行脱苄基反应,定量得到7-O-(ω-卤代烷基)-3-O-甲基槲皮素(11 - 14)和7-O-(ω-羟烷基)-3-O-甲基槲皮素衍生物(15, 16)。对所有化合物进行了抗脊髓灰质炎病毒和HIV病毒的抗病毒活性测试。