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2-oxo-4-(pyridin-4-ylmethylamino)-1H-quinoline-3-carboxylic acid | 1314000-42-4

中文名称
——
中文别名
——
英文名称
2-oxo-4-(pyridin-4-ylmethylamino)-1H-quinoline-3-carboxylic acid
英文别名
——
2-oxo-4-(pyridin-4-ylmethylamino)-1H-quinoline-3-carboxylic acid化学式
CAS
1314000-42-4
化学式
C16H13N3O3
mdl
——
分子量
295.298
InChiKey
YOPSXVFQQBEMDI-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):
    2.3
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.06
  • 拓扑面积:
    91.3
  • 氢给体数:
    3
  • 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

  • 作为产物:
    描述:
    4-甲氨基吡啶4-氯-2-氧代-1H-喹啉-3-羧酸三乙胺 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以94%的产率得到2-oxo-4-(pyridin-4-ylmethylamino)-1H-quinoline-3-carboxylic acid
    参考文献:
    名称:
    4-Hydroxy-2-quinolones. 195*. Synthesis of novel, potential analgesics based on 4-(hetarylmethyl)amino-2-oxo-1,2-dihydro-quinoline-3-carboxylic acids
    摘要:
    From the viewpoint of the method of bioisosteric replacement we have carried out the synthesis of a series of 4-(hetarylmethyl)amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acids. For several examples it has been shown experimentally that the aromatic ring in the benzyl fragment of 4-benzylamino-2-oxo-1,2-dihydroquinoline-3-carboxylic acid can be replaced by an isosteric heterocycle without lowering the analgesic properties.
    DOI:
    10.1007/s10593-011-0721-4
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文献信息

  • 4-Hydroxy-2-quinolones. 195*. Synthesis of novel, potential analgesics based on 4-(hetarylmethyl)amino-2-oxo-1,2-dihydro-quinoline-3-carboxylic acids
    作者:I. V. Ukrainets、E. V. Mospanova、L. V. Savchenkova、S. I. Yankovich
    DOI:10.1007/s10593-011-0721-4
    日期:2011.4
    From the viewpoint of the method of bioisosteric replacement we have carried out the synthesis of a series of 4-(hetarylmethyl)amino-2-oxo-1,2-dihydroquinoline-3-carboxylic acids. For several examples it has been shown experimentally that the aromatic ring in the benzyl fragment of 4-benzylamino-2-oxo-1,2-dihydroquinoline-3-carboxylic acid can be replaced by an isosteric heterocycle without lowering the analgesic properties.
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