7-Chloro-3-cyclohexyl-3,4-dihydro-2H,10H-acridine-1,9-dione | 144128-86-9

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 7-Chloro-3-cyclohexyl-3,4-dihydro-2H,10H-acridine-1,9-dione
• CAS: 144128-86-9
• 化学式: C₁₉H₂₀ClNO₂
• 分子量: 329.826
• InChiKey: CKWWXAKLZAWBTA-UHFFFAOYSA-N

物化性质

• 沸点：
  493.8±45.0 °C(Predicted)
• 密度：
  1.30±0.1 g/cm3(Predicted)

反应信息

• 作为反应物：
  描述：

  7-Chloro-3-cyclohexyl-3,4-dihydro-2H,10H-acridine-1,9-dione 、 N,N-二甲基-1,3-二氨基丙烷 以 乙醇 为溶剂， 反应 1.5h， 以75%的产率得到7-Chloro-3-cyclohexyl-1-[(E)-3-dimethylamino-propylimino]-1,3,4,10-tetrahydro-2H-acridin-9-one
  参考文献：
  名称：

  Antimalarial drugs. 64. Synthesis and antimalarial properties of 1-imino derivatives of 7-chloro-3-substituted-3,4-dihydro-1,9(2H,10H)-acridinediones and related structures

  摘要：

  To improve upon the activity and properties of the 3-aryl-7-chloro-3,4-dihydro-1,9(2H,10H)-acridinediones, a variety of 1-[(alkylamino)alkylene]imino derivatives (3) were prepared and shown to be highly active antimalarial agents in both rodents and primates. Among structural modifications prepared, including N-10-alkyl and C2-substituted analogs, removal of the C-9 oxygen, and introduction of an imino side chain at C-9, the imines of the N-10-H acridinediones were the most active compounds obtained. The [3-(NN-dimethylamino)propyl]imino derivative of 7-chloro-3-(2,4-dichlorophenyl)-3,4-dihydro-1,9(2H,10H)-acridinedione (9aa) proved to be highly active in advanced studies in primates.

  DOI：

  10.1021/jm00097a001