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4-hydroxy-6-methyl-3-propionylpyridin-2(1H)-one | 7135-82-2

中文名称
——
中文别名
——
英文名称
4-hydroxy-6-methyl-3-propionylpyridin-2(1H)-one
英文别名
3-Propionyl-4-hydroxy-6-methyl-2-pyridon;4-hydroxy-6-methyl-3-propionyl-1H-pyridin-2-one;2(1H)-Pyridone, 4-hydroxy-6-methyl-3-propionyl-;4-hydroxy-6-methyl-3-propanoyl-1H-pyridin-2-one
4-hydroxy-6-methyl-3-propionylpyridin-2(1H)-one化学式
CAS
7135-82-2
化学式
C9H11NO3
mdl
——
分子量
181.191
InChiKey
XJWVHLCIZXERQK-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):
    0.9
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    66.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    4-hydroxy-6-methyl-3-propionylpyridin-2(1H)-one盐酸羟胺碳酸氢钠 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以65%的产率得到4-hydroxy-3-[(1E)-N-hydroxypropaneimidoyl]-6-methylpyridin-2(1H)-one
    参考文献:
    名称:
    Synthesis of Functionalized Pyrano[3,2‐c]pyridines and Their Transformations to 4‐Hydroxy‐3[(1E)‐N‐hydroxyalkanimidoyl]pyridones
    摘要:
    Reaction of 4-hydroxy-6-methyl-2(1H)-pyridones 1a and 4-hydroxy-1,6-dimethyl-2(1H)-pyridones 1b with diethyl malonates 2a-e leads to the formation of pyrano[3,2-c]pyridines 4a-j. Degradation of 4a-i affords the corresponding ketones 6a-i. Condensation of ketones 6a-i with hydroxyl amine or phenyl hydrazine hydrochloride is described.
    DOI:
    10.1080/00397910701547995
  • 作为产物:
    描述:
    4-hydroxy-3,7-dimethyl-6H-pyrano[3,2-c]pyridine-2,5-dione 在 sodium hydroxide 作用下, 以 乙二醇 为溶剂, 反应 2.0h, 以70%的产率得到4-hydroxy-6-methyl-3-propionylpyridin-2(1H)-one
    参考文献:
    名称:
    Synthesis of Functionalized Pyrano[3,2‐c]pyridines and Their Transformations to 4‐Hydroxy‐3[(1E)‐N‐hydroxyalkanimidoyl]pyridones
    摘要:
    Reaction of 4-hydroxy-6-methyl-2(1H)-pyridones 1a and 4-hydroxy-1,6-dimethyl-2(1H)-pyridones 1b with diethyl malonates 2a-e leads to the formation of pyrano[3,2-c]pyridines 4a-j. Degradation of 4a-i affords the corresponding ketones 6a-i. Condensation of ketones 6a-i with hydroxyl amine or phenyl hydrazine hydrochloride is described.
    DOI:
    10.1080/00397910701547995
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文献信息

  • Synthesis of Functionalized Pyrano[3,2‐<i>c</i>]pyridines and Their Transformations to 4‐Hydroxy‐3[(1<i>E</i>)‐<i>N</i>‐hydroxyalkanimidoyl]pyridones
    作者:Farag A. El‐Essawy、Ahmed F. Khattab、Magdy A. Zahran、Sherif H. Gomaa
    DOI:10.1080/00397910701547995
    日期:2007.9.1
    Reaction of 4-hydroxy-6-methyl-2(1H)-pyridones 1a and 4-hydroxy-1,6-dimethyl-2(1H)-pyridones 1b with diethyl malonates 2a-e leads to the formation of pyrano[3,2-c]pyridines 4a-j. Degradation of 4a-i affords the corresponding ketones 6a-i. Condensation of ketones 6a-i with hydroxyl amine or phenyl hydrazine hydrochloride is described.
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