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1-(4-methyl-2-oxo-1,2,5,6,7,8-hexahydroquinolin-3-yl)pyridin-1-ium chloride | 1607833-74-8

中文名称
——
中文别名
——
英文名称
1-(4-methyl-2-oxo-1,2,5,6,7,8-hexahydroquinolin-3-yl)pyridin-1-ium chloride
英文别名
——
1-(4-methyl-2-oxo-1,2,5,6,7,8-hexahydroquinolin-3-yl)pyridin-1-ium chloride化学式
CAS
1607833-74-8
化学式
C15H17N2O*Cl
mdl
——
分子量
276.766
InChiKey
GNZGEHBRZHNBBC-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):
    -1.16
  • 重原子数:
    19.0
  • 可旋转键数:
    1.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    36.74
  • 氢给体数:
    1.0
  • 氢受体数:
    1.0

反应信息

  • 作为反应物:
    描述:
    1-(4-methyl-2-oxo-1,2,5,6,7,8-hexahydroquinolin-3-yl)pyridin-1-ium chloride一水合肼 作用下, 以 为溶剂, 反应 3.0h, 以57%的产率得到
    参考文献:
    名称:
    Synthesis of 3-Aminopyridin-2(1H)-Ones and 1H-Pyrido[2,3-b][1,4]Oxazin-2(3H)-Ones
    摘要:
    The interaction of 1,3-diketones with chloroacetamide produced N-(3-oxoalkenyl)chloroacetamides. Heating of N-(3-oxoalkenyl)chloroacetamides with an excess of pyridine in ethanol or butanol led to the formation of pyridin-2(1De)-ones, substituted with a pyridine ring at position 3. The reactions of these compounds with hydrazine hydrate produced 3-aminopyridin-2(1De)-ones. The synthesis of 1H-pyrido[2,3-b][1, 4]oxazin-2(3H)-ones was accomplished by a reaction of 3-aminopyridin-2(1De)-ones with chloroacetyl chloride.
    DOI:
    10.1007/s10593-014-1464-9
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis of 3-Aminopyridin-2(1H)-Ones and 1H-Pyrido[2,3-b][1,4]Oxazin-2(3H)-Ones
    摘要:
    The interaction of 1,3-diketones with chloroacetamide produced N-(3-oxoalkenyl)chloroacetamides. Heating of N-(3-oxoalkenyl)chloroacetamides with an excess of pyridine in ethanol or butanol led to the formation of pyridin-2(1De)-ones, substituted with a pyridine ring at position 3. The reactions of these compounds with hydrazine hydrate produced 3-aminopyridin-2(1De)-ones. The synthesis of 1H-pyrido[2,3-b][1, 4]oxazin-2(3H)-ones was accomplished by a reaction of 3-aminopyridin-2(1De)-ones with chloroacetyl chloride.
    DOI:
    10.1007/s10593-014-1464-9
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