5-(2,4-dichlorophenyl)-4-methyl-1,3-cyclohexanedione | 89756-75-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 5-(2,4-dichlorophenyl)-4-methyl-1,3-cyclohexanedione
• 英文别名: 1,3-Cyclohexanedione, 5-(2,4-dichlorophenyl)-4-methyl-；5-(2,4-dichlorophenyl)-4-methylcyclohexane-1,3-dione
• CAS: 89756-75-2
• 化学式: C₁₃H₁₂Cl₂O₂
• 分子量: 271.143
• InChiKey: XQCOAOIYBYPUSD-UHFFFAOYSA-N

物化性质

• 熔点：
  182-184 °C(Solv: acetonitrile (75-05-8))
• 沸点：
  395.5±42.0 °C(Predicted)
• 密度：
  1.306±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  17
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  34.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  5-(2,4-dichlorophenyl)-4-methyl-1,3-cyclohexanedione 在 sodium hydride 作用下， 以 乙醇 为溶剂， 反应 6.5h， 生成 7-Chloro-3-(2,4-dichloro-phenyl)-1-[(E)-3-dimethylamino-propylimino]-2-methyl-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
• 作为产物：
  描述：

  4-(2,4-二氯苯基)-3-甲基丁-3-烯-2-酮 在 sodium hydroxide 、 硫酸 、 sodium ethanolate 作用下， 以 乙醇 为溶剂， 反应 6.0h， 生成 5-(2,4-dichlorophenyl)-4-methyl-1,3-cyclohexanedione
  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

文献信息

• Werbel; Hung; McNamara, European Journal of Medicinal Chemistry, 1985, vol. 20, # 4, p. 363 - 370
  作者：Werbel、Hung、McNamara、Ortwine

  DOI：——

  日期：——
• HUNG, J.;MCNAMARA, D. J.;WERBEL, L. M., J. HETEROCYCL. CHEM., 1983, 20, N 6, 1575-1580
  作者：HUNG, J.、MCNAMARA, D. J.、WERBEL, L. M.

  DOI：——

  日期：——
• WERBEL, L. M.;HUNG, J.;MCNAMARA, D.;ORTWINE, D. F., EUR. J. MED. CHEM., 1985, 20, N 4, 363-370
  作者：WERBEL, L. M.、HUNG, J.、MCNAMARA, D.、ORTWINE, D. F.

  DOI：——

  日期：——
• 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
  作者：Stephen J. Kesten、Margaret J. Degnan、Jocelyn Hung、Dennis J. McNamara、Daniel F. Ortwine、Susan E. Uhlendorf、Leslie M. Werbel

  DOI：10.1021/jm00097a001

  日期：1992.9

  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.