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5-bromo-4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-1,5-diphenyl-2,5-dihydro-1H-imidazol-2-one | 1178563-13-7

中文名称
——
中文别名
——
英文名称
5-bromo-4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-1,5-diphenyl-2,5-dihydro-1H-imidazol-2-one
英文别名
5-Bromo-4-(4-hydroxy-2-oxo-2h-chromen-3-yl)-1,5-diphenyl-2,5-dihydro-1h-imidazol-2-one;5-bromo-4-(4-hydroxy-2-oxochromen-3-yl)-1,5-diphenylimidazol-2-one
5-bromo-4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-1,5-diphenyl-2,5-dihydro-1H-imidazol-2-one化学式
CAS
1178563-13-7
化学式
C24H15BrN2O4
mdl
——
分子量
475.298
InChiKey
RBKZBTVCSAWYJR-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):
    4.9
  • 重原子数:
    31
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    79.2
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    5-(4-hydroxy-2-oxo-2H-chromen-3-yl)-3,4-diphenyl-2,3-dihydro-1H-imidazol-2-one 在 作用下, 以 溶剂黄146 为溶剂, 反应 1.0h, 以56%的产率得到5-bromo-4-(4-hydroxy-2-oxo-2H-chromen-3-yl)-1,5-diphenyl-2,5-dihydro-1H-imidazol-2-one
    参考文献:
    名称:
    Reaction of 4-hydroxycoumarin with arylglyoxals and ureas
    摘要:
    One-pot condensation of 4-hydroxycoumarin with arylglyoxals and ureas gave 4-aryl-5-(4-hydroxy-2-oxo-2H-chromen-3-yl)-1H-imidazol-2(3H)-ones. The same compounds may be obtained from aroylbis(4-hydroxy-2-oxo-2H-chromen-3-yl)methanes and urea. The reaction of 4-bromobenzaldehyde with 4-hydroxycoumarin in the presence of urea led to the formation of the corresponding Michael adduct without participation of urea.
    DOI:
    10.1134/s1070428009010151
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文献信息

  • Reaction of 4-hydroxycoumarin with arylglyoxals and ureas
    作者:N. N. Kolos、L. L. Gozalishvili、E. N. Sivokon’、I. V. Knyazeva
    DOI:10.1134/s1070428009010151
    日期:2009.1
    One-pot condensation of 4-hydroxycoumarin with arylglyoxals and ureas gave 4-aryl-5-(4-hydroxy-2-oxo-2H-chromen-3-yl)-1H-imidazol-2(3H)-ones. The same compounds may be obtained from aroylbis(4-hydroxy-2-oxo-2H-chromen-3-yl)methanes and urea. The reaction of 4-bromobenzaldehyde with 4-hydroxycoumarin in the presence of urea led to the formation of the corresponding Michael adduct without participation of urea.
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