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6-Butyl-3-methyl-1H-quinoxalin-2-one | 868771-48-6

中文名称
——
中文别名
——
英文名称
6-Butyl-3-methyl-1H-quinoxalin-2-one
英文别名
——
6-Butyl-3-methyl-1H-quinoxalin-2-one化学式
CAS
868771-48-6
化学式
C13H16N2O
mdl
——
分子量
216.283
InChiKey
NZEWFVXDYRYBMX-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):
    2.6
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    41.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    6-Butyl-3-methyl-1H-quinoxalin-2-one碘甲烷 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 以67%的产率得到6-Butyl-1,3-dimethylquinoxalin-2-one
    参考文献:
    名称:
    Synthesis of Substituted 1,3-Dimethyl-1H-quinoxalin-2-ones from Aniline Derivatives
    摘要:
    Substituted 1,3-dimethyl-1H-quinoxalin-2-ones (7) have been synthesized through the procedures of acylation, nitration, reduction, intramolecular alkylation, oxidation, and N-methylation starting from 3,4-disubstituted aniline.
    DOI:
    10.3987/com-05-10461
  • 作为产物:
    描述:
    4-正丁基苯胺sodium hydroxide硫酸 、 ammonium chloride 、 双氧水硝酸铁粉碳酸氢钠溶剂黄146 、 sodium iodide 作用下, 以 N,N-二甲基甲酰胺甲苯乙腈 为溶剂, 生成 6-Butyl-3-methyl-1H-quinoxalin-2-one
    参考文献:
    名称:
    Novel Approach to 3‐Methyl‐1H‐quinoxalin‐2‐ones
    摘要:
    A novel approach to the synthesis of 3-methyl-1H-quinoxalin-2-ones has been described. These compounds were regioselectively prepared by starting from substituted phenylamines and alpha-chloropropionyl chloride through the efficient procedures of acylation, nitration, reduction, intramolecular alkylation, and oxidation.
    DOI:
    10.1080/00397910500213880
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文献信息

  • Novel Approach to 3‐Methyl‐1H‐quinoxalin‐2‐ones
    作者:Xun Li、Donghua Wang、Jifeng Wu、Wenfang Xu
    DOI:10.1080/00397910500213880
    日期:2005.10
    A novel approach to the synthesis of 3-methyl-1H-quinoxalin-2-ones has been described. These compounds were regioselectively prepared by starting from substituted phenylamines and alpha-chloropropionyl chloride through the efficient procedures of acylation, nitration, reduction, intramolecular alkylation, and oxidation.
  • Synthesis of Substituted 1,3-Dimethyl-1H-quinoxalin-2-ones from Aniline Derivatives
    作者:Xun Li、Donghua Wang、Jifeng Wu、Wenfang Xu
    DOI:10.3987/com-05-10461
    日期:——
    Substituted 1,3-dimethyl-1H-quinoxalin-2-ones (7) have been synthesized through the procedures of acylation, nitration, reduction, intramolecular alkylation, oxidation, and N-methylation starting from 3,4-disubstituted aniline.
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