作者:Sabrina Castellano、Giorgio Stefancich、Paolo La Colla、Chiara Musiu
DOI:10.1002/jhet.5570370621
日期:2000.11
Two novel tricyclic triazepinones structurally related to the reverse transcriptase inhibitor nevirapine were prepared from N-(2-nitrophenyl)- and N-(3-nitro-2-pyridinyl)-1H-pyrrol-1-amine. The synthetic sequence includes alkylation, reduction of the nitro group, triphosgene reaction followed by intramolecular cyclization. Activity of the two compounds against the HIV-1 multiplication in acutely infected
从N-(2-硝基苯基)-和N-(3-硝基-2-吡啶基)-1 H-吡咯-1-胺制备了两个与逆转录酶抑制剂奈韦拉平结构相关的新型三环三氮杂吡啶酮。合成序列包括烷基化,硝基还原,三光气反应,然后进行分子内环化。还报道了两种化合物对急性感染细胞中HIV-1繁殖的活性。