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2-((4,5-dihydro-4-methylpyrrolo[1,2-a]quinoxalin-4-yl)methoxy)ethanol | 1176667-04-1

中文名称
——
中文别名
——
英文名称
2-((4,5-dihydro-4-methylpyrrolo[1,2-a]quinoxalin-4-yl)methoxy)ethanol
英文别名
2-[(4-methyl-5H-pyrrolo[1,2-a]quinoxalin-4-yl)methoxy]ethanol
2-((4,5-dihydro-4-methylpyrrolo[1,2-a]quinoxalin-4-yl)methoxy)ethanol化学式
CAS
1176667-04-1
化学式
C15H18N2O2
mdl
——
分子量
258.32
InChiKey
QBAWJONYFJNZSQ-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):
    1.3
  • 重原子数:
    19
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    46.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    丙炔醇乙氧基化合物1-(2-氨基苯基)吡咯 在 platinum(II) bromde 作用下, 以 甲醇 为溶剂, 反应 12.0h, 以88%的产率得到2-((4,5-dihydro-4-methylpyrrolo[1,2-a]quinoxalin-4-yl)methoxy)ethanol
    参考文献:
    名称:
    Platinum-Catalyzed Formal Markownikoff’s Hydroamination/Hydroarylation Cascade of Terminal Alkynes Assisted by Tethered Hydroxyl Groups
    摘要:
    An efficient method for Markownikoff's hydroamination-hydroarylation of alkynols using PtBr2 as catalyst has been developed. The platinum-catalyzed reactions of alkynols with amino group containing aromatics were achieved in methanol over a reaction time of 6-24 h and temperature ranging from rt to 80 degrees C. This method works well for a variety of alkynols and aromatic amino compounds to give substituted pyrrolo[1,2-a]quinoxalines and indolo[3,2-c]quinolines in good to excellent yields.
    DOI:
    10.1021/jo901200j
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文献信息

  • Platinum-Catalyzed Formal Markownikoff’s Hydroamination/Hydroarylation Cascade of Terminal Alkynes Assisted by Tethered Hydroxyl Groups
    作者:Nitin T. Patil、Rahul D. Kavthe、Vivek S. Raut、Vaddu V. N. Reddy
    DOI:10.1021/jo901200j
    日期:2009.8.21
    An efficient method for Markownikoff's hydroamination-hydroarylation of alkynols using PtBr2 as catalyst has been developed. The platinum-catalyzed reactions of alkynols with amino group containing aromatics were achieved in methanol over a reaction time of 6-24 h and temperature ranging from rt to 80 degrees C. This method works well for a variety of alkynols and aromatic amino compounds to give substituted pyrrolo[1,2-a]quinoxalines and indolo[3,2-c]quinolines in good to excellent yields.
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