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7-氯-9-羟基-3-(4-甲基苯基)-3,4-二氢-1(2H)-吖啶酮 | 144155-05-5

中文名称
7-氯-9-羟基-3-(4-甲基苯基)-3,4-二氢-1(2H)-吖啶酮
中文别名
——
英文名称
7-Chloro-3-p-tolyl-3,4-dihydro-2H,10H-acridine-1,9-dione
英文别名
7-Chloro-3-(4-methylphenyl)-3,4-dihydro-1,9(2H,10H)-acridinedione;7-chloro-3-(4-methylphenyl)-2,3,4,10-tetrahydroacridine-1,9-dione
7-氯-9-羟基-3-(4-甲基苯基)-3,4-二氢-1(2H)-吖啶酮化学式
CAS
144155-05-5
化学式
C20H16ClNO2
mdl
——
分子量
337.806
InChiKey
QXFLSUBIMJDWAZ-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    514.6±50.0 °C(Predicted)
  • 密度:
    1.35±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    24
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    46.2
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    7-氯-9-羟基-3-(4-甲基苯基)-3,4-二氢-1(2H)-吖啶酮N,N-二甲基-1,3-二氨基丙烷乙醇 为溶剂, 反应 1.5h, 以68%的产率得到7-Chloro-1-[(E)-3-dimethylamino-propylimino]-3-p-tolyl-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:
    7-Chloro-10-hydroxy-3-p-tolyl-3,4-dihydro-2H,10H-acridine-1,9-dione三氯化磷 作用下, 以 氯仿 为溶剂, 反应 1.0h, 以74%的产率得到7-氯-9-羟基-3-(4-甲基苯基)-3,4-二氢-1(2H)-吖啶酮
    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
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文献信息

  • 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.
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