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2-(4-(2-hydroxyphenyl)-2-(pyrimidin-2-yl)-1H-imidazol-5-yl)phenol | 1201275-66-2

中文名称
——
中文别名
——
英文名称
2-(4-(2-hydroxyphenyl)-2-(pyrimidin-2-yl)-1H-imidazol-5-yl)phenol
英文别名
2-[4-(2-hydroxyphenyl)-2-pyrimidin-2-yl-1H-imidazol-5-yl]phenol
2-(4-(2-hydroxyphenyl)-2-(pyrimidin-2-yl)-1H-imidazol-5-yl)phenol化学式
CAS
1201275-66-2
化学式
C19H14N4O2
mdl
——
分子量
330.346
InChiKey
GLEBZCKSRCNKDT-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):
    2.7
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    94.9
  • 氢给体数:
    3
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-氰基嘧啶水杨醛 在 ammonium acetate 作用下, 反应 0.43h, 以83%的产率得到2-(4-(2-hydroxyphenyl)-2-(pyrimidin-2-yl)-1H-imidazol-5-yl)phenol
    参考文献:
    名称:
    Microwave Enabled Umpulong Mechanism Based Rapid and Efficient Four- and Six-Component Domino Formations of 2-(2′-Azaaryl)imidazoles and anti-1,2-Diarylethylbenzamides
    摘要:
    Concise and efficient six-component and four-component domino approaches to anti-1,2-diarylethylbenzamides and highly Substituted 2-(2'-azaaryl)imidazoles have been developed under solvent-free and microwave-irradiation conditions. The reactions showed a broad scope of substrates in which a wide range of common commercial aromatic aldehydes and heteroaryl nitriles can be used. The syntheses were Finished within short periods (15-34 min) with good to excellent chemical yields and stereoselectivity that avoided tedious workup isolations. New mechanisms involving an umpolung have been proposed for these two reaction processes.
    DOI:
    10.1021/jo902204s
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