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4-N-[3-(5-chloro-1H-pyrazol-3-yl)quinoxalin-2-yl]-1-N,1-N-diethylpentane-1,4-diamine | 204654-34-2

中文名称
——
中文别名
——
英文名称
4-N-[3-(5-chloro-1H-pyrazol-3-yl)quinoxalin-2-yl]-1-N,1-N-diethylpentane-1,4-diamine
英文别名
——
4-N-[3-(5-chloro-1H-pyrazol-3-yl)quinoxalin-2-yl]-1-N,1-N-diethylpentane-1,4-diamine化学式
CAS
204654-34-2
化学式
C20H27ClN6
mdl
——
分子量
386.928
InChiKey
AQJQYPTVLJPATL-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.4
  • 重原子数:
    27
  • 可旋转键数:
    9
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    69.7
  • 氢给体数:
    2
  • 氢受体数:
    5

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

反应信息

  • 作为反应物:
    描述:
    4-N-[3-(5-chloro-1H-pyrazol-3-yl)quinoxalin-2-yl]-1-N,1-N-diethylpentane-1,4-diamine 在 palladium on activated charcoal ammonium formate 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以65%的产率得到1-N,1-N-diethyl-4-N-[3-(1H-pyrazol-5-yl)quinoxalin-2-yl]pentane-1,4-diamine
    参考文献:
    名称:
    Syntheses in the Series of Pyrazolyl-substituted Quinoxalines
    摘要:
    Starting from 3-(3-chloro-1H-pyrazol-5-yl)-1H-quinoxalin-2-one (2), a dihydroquinoxalinone derivative (6) was synthesised as potential HIV-1 reverse transcriptase inhibitor. Moreover, a series of N(4)-[3-(3-pyrazolyl)-2-quinoxalinyl]-N(1),N(1)-diethyl-1,4-pentanediamines (compounds of type B) and N-[3-(3-pyrazolyl)-2-quinoxalinyl]-N-(3-pyridyl)methylamines (11-13)- structurally related to antimalarial agents - could be prepared via the 2-chloro-3-[3(5)-chloro-1H-pyrazol-5(3)-yl]quinoxaline (7). The position of the alkyl substituent on the pyrazole nitrogen was determined unequivocally from NOE difference experiments or X-Ray structure analysis.
    DOI:
    10.3987/com-97-7965
  • 作为产物:
    参考文献:
    名称:
    Syntheses in the Series of Pyrazolyl-substituted Quinoxalines
    摘要:
    Starting from 3-(3-chloro-1H-pyrazol-5-yl)-1H-quinoxalin-2-one (2), a dihydroquinoxalinone derivative (6) was synthesised as potential HIV-1 reverse transcriptase inhibitor. Moreover, a series of N(4)-[3-(3-pyrazolyl)-2-quinoxalinyl]-N(1),N(1)-diethyl-1,4-pentanediamines (compounds of type B) and N-[3-(3-pyrazolyl)-2-quinoxalinyl]-N-(3-pyridyl)methylamines (11-13)- structurally related to antimalarial agents - could be prepared via the 2-chloro-3-[3(5)-chloro-1H-pyrazol-5(3)-yl]quinoxaline (7). The position of the alkyl substituent on the pyrazole nitrogen was determined unequivocally from NOE difference experiments or X-Ray structure analysis.
    DOI:
    10.3987/com-97-7965
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文献信息

  • Syntheses in the Series of Pyrazolyl-substituted Quinoxalines
    作者:Barbara Matuszczak、Kurt Mereiter
    DOI:10.3987/com-97-7965
    日期:——
    Starting from 3-(3-chloro-1H-pyrazol-5-yl)-1H-quinoxalin-2-one (2), a dihydroquinoxalinone derivative (6) was synthesised as potential HIV-1 reverse transcriptase inhibitor. Moreover, a series of N(4)-[3-(3-pyrazolyl)-2-quinoxalinyl]-N(1),N(1)-diethyl-1,4-pentanediamines (compounds of type B) and N-[3-(3-pyrazolyl)-2-quinoxalinyl]-N-(3-pyridyl)methylamines (11-13)- structurally related to antimalarial agents - could be prepared via the 2-chloro-3-[3(5)-chloro-1H-pyrazol-5(3)-yl]quinoxaline (7). The position of the alkyl substituent on the pyrazole nitrogen was determined unequivocally from NOE difference experiments or X-Ray structure analysis.
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