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1-((7-chloroquinolin-4-yl)amino)-2-methyl-5-(4-nitrophenyl)-1H-pyrrole-3-(N,N-diethyl)-carboxamide | 1251469-24-5

中文名称
——
中文别名
——
英文名称
1-((7-chloroquinolin-4-yl)amino)-2-methyl-5-(4-nitrophenyl)-1H-pyrrole-3-(N,N-diethyl)-carboxamide
英文别名
——
1-((7-chloroquinolin-4-yl)amino)-2-methyl-5-(4-nitrophenyl)-1H-pyrrole-3-(N,N-diethyl)-carboxamide化学式
CAS
1251469-24-5
化学式
C25H24ClN5O3
mdl
——
分子量
477.95
InChiKey
HCUMFRGTKJSHDS-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

  • 熔点:
    276-278.3 °C
  • 沸点:
    711.4±70.0 °C(predicted)
  • 密度:
    1.32±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.93
  • 重原子数:
    34.0
  • 可旋转键数:
    7.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    93.3
  • 氢给体数:
    1.0
  • 氢受体数:
    6.0

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:
    1-((7-chloroquinolin-4-yl)amino)-2-methyl-5-(4-nitrophenyl)-1H-pyrrole-3-(N,N-diethyl)-carboxamide铁粉溶剂黄146 、 sodium hydroxide 作用下, 以 甲醇二氯甲烷 为溶剂, 以71%的产率得到5-(4-aminophenyl)-1-((7-chloroquinolin-4-yl)amino)-2-methyl-1H-pyrrole-3-(N,N-diethyl)carboxamide
    参考文献:
    名称:
    Synthesis, antimalarial activity, and cellular toxicity of new arylpyrrolylaminoquinolines
    摘要:
    A set of nine new arylpyrrolyl derivatives of 7-chloro-4-aminoquinoline, characterized by different substituents on the phenyl ring or different distance between the pyrrolic nitrogen and the 4-aminoquinoline, has been synthesized and tested for their activity against D-10 (CQ-S) and W-2 (CQ-R) strains of Plasmodium falciparum. All compounds exhibited activity against the CQ-S strain in the low nM range, comparable to that of chloroquine. Some of them were also highly active against the CQ-R strain and not toxic against normal cells. The antimalarial activity of this new class of compounds seems to be related to the inhibition of heme detoxification process of parasites, as in the case of chloroquine. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.08.001
  • 作为产物:
    描述:
    1-((7-chloroquinolin-4-yl)amino)-2-methyl-5-(4-nitrophenyl)-1H-pyrrole-3-carboxylic acid二乙胺1-羟基苯并三唑N,N'-二环己基碳二亚胺 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 以74%的产率得到1-((7-chloroquinolin-4-yl)amino)-2-methyl-5-(4-nitrophenyl)-1H-pyrrole-3-(N,N-diethyl)-carboxamide
    参考文献:
    名称:
    Synthesis, antimalarial activity, and cellular toxicity of new arylpyrrolylaminoquinolines
    摘要:
    A set of nine new arylpyrrolyl derivatives of 7-chloro-4-aminoquinoline, characterized by different substituents on the phenyl ring or different distance between the pyrrolic nitrogen and the 4-aminoquinoline, has been synthesized and tested for their activity against D-10 (CQ-S) and W-2 (CQ-R) strains of Plasmodium falciparum. All compounds exhibited activity against the CQ-S strain in the low nM range, comparable to that of chloroquine. Some of them were also highly active against the CQ-R strain and not toxic against normal cells. The antimalarial activity of this new class of compounds seems to be related to the inhibition of heme detoxification process of parasites, as in the case of chloroquine. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2010.08.001
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