3-甲氧基-4-硝基苯胺置于palladium On Activated Charcoal 吡啶,盐酸,氢气体系中,用 甲醇 作为反应溶剂,20.0 °C,202.65 Kpa 条件下,反应 4.25H,反应生成 胺苯吖啶
参考文献:Potential Antitumor Agents. 48. 3'-Dimethylamino Derivatives Of Amsacrine: Redox Chemistry And In Vivo Solid Tumor Activity
标题:Potential Antitumor Agents. 48. 3'-Dimethylamino Derivatives Of Amsacrine: Redox Chemistry And In Vivo Solid Tumor Activity
摘要:Structure-Activity Relationships For A Series Of Acridine-Substituted 3'-N(Ch3)2 Derivatives Of The Clinical Antileukemic Drug Amsacrine (1) Are Reported. The Parent (Unsubstituted) Compound 3 Has Activity Against The Lewis Lung Solid Tumor That Is Superior To Amsacrine (1),The New Clinical Amsacrine Analogue 4,And The Recently Developed 3'-Nhch3 Derivative 2. Although The Compounds Generally Bind Less Well To Dna And Are Less Dose Potent In Vivo Than Either Their Amsacrine (3'-och3) Or 3'-Nhch3 Analogues,They Show Very High Levels Of Antitumor Activity,With The 4-och3 Derivative Capable Of Effecting 100% Cures Of The Lewis Lung Solid Tumor. The Broad Structure-Activity Relationships For Acridine Substitution More Closely Resemble Those Of The Amsacrine Than The 3'-Nhch3 Series,With 4-Substituted And 4,5-Disubstituted Compounds Showing The Highest Activity.
DOI:10.1021/jm00387A012