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2-hydroxy-1-nonyl-4-oxo-N-(pyrazin-2-yl)-1,4-dihydroquinoline-3-carboxamide | 384376-45-8

中文名称
——
中文别名
——
英文名称
2-hydroxy-1-nonyl-4-oxo-N-(pyrazin-2-yl)-1,4-dihydroquinoline-3-carboxamide
英文别名
4-hydroxy-1-nonyl-2-oxo-N-pyrazin-2-ylquinoline-3-carboxamide
2-hydroxy-1-nonyl-4-oxo-N-(pyrazin-2-yl)-1,4-dihydroquinoline-3-carboxamide化学式
CAS
384376-45-8
化学式
C23H28N4O3
mdl
——
分子量
408.5
InChiKey
GXRCZNUMISGUBY-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):
    4.6
  • 重原子数:
    30
  • 可旋转键数:
    10
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.39
  • 拓扑面积:
    95.4
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    参考文献:
    名称:
    4-Hydroxy-2-quinolones. 168*. Synthesis, chemical and antitubercular properties of 1-R-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid pyrazin-2-ylamides
    摘要:
    1-R-4-Hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylic acid pyrazin-2-ylamides have been synthesized as potential antitubercular agents. In contrast to pyrimidin-2-ylamides the compounds prepared are brominated by molecular bromine in glacial acetic acid at position 6 of the quinolone ring rather than in the amide part of the molecule. The 1-N-allyl derivative behaves similarly but undergoes halocyclization to give 2-bromomethyl-5-oxo-1,2-dihydro-5H-oxazolo[3,2-a] quinoline-4-carboxylic acid pyrazin-2-ylamide. A comparative analysis of the antimycobacterial properties of the synthesized compounds and their isomeric pyrimidin-2-ylamides has been carried out.
    DOI:
    10.1007/s10593-009-0384-6
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