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2-(3-methoxyphenyl)-1-phenyl-4,5-dihydro-1H-imidazole | 1427476-04-7

中文名称
——
中文别名
——
英文名称
2-(3-methoxyphenyl)-1-phenyl-4,5-dihydro-1H-imidazole
英文别名
2-(3-Methoxyphenyl)-1-phenyl-4,5-dihydroimidazole;2-(3-methoxyphenyl)-1-phenyl-4,5-dihydroimidazole
2-(3-methoxyphenyl)-1-phenyl-4,5-dihydro-1H-imidazole化学式
CAS
1427476-04-7
化学式
C16H16N2O
mdl
——
分子量
252.316
InChiKey
JWPKQGXYQQAZDN-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:
    19
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.19
  • 拓扑面积:
    24.8
  • 氢给体数:
    0
  • 氢受体数:
    2

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    碘苯2-(3-甲氧基苯基)-4,5-二氢-1H-咪唑caesium carbonate 、 copper(I) bromide 作用下, 以 N-甲基吡咯烷酮 为溶剂, 反应 18.0h, 以78%的产率得到2-(3-methoxyphenyl)-1-phenyl-4,5-dihydro-1H-imidazole
    参考文献:
    名称:
    Copper-Catalyzed N-Arylation of 2-Imidazolines with Aryl Iodides
    摘要:
    The first copper-catalyzed N-arylation of 2-imidazolines is described. The reaction affords compounds with desirable lead-like characteristics in high yield with practical simplicity under inexpensive, "ligand-free" conditions. The cross coupling was successful with electron-rich and electron-poor aromatic iodides. Substrates bearing halides, esters, nitriles, and free hydroxyls are well tolerated, providing reactive handles for further functionalization, as are pyridines. In addition, the regioselective N-arylation of a 4-substituted imidazoline is reported.
    DOI:
    10.1021/jo400120r
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文献信息

  • Copper-Catalyzed <i>N</i>-Arylation of 2-Imidazolines with Aryl Iodides
    作者:Owen A. Davis、Matthew Hughes、James A. Bull
    DOI:10.1021/jo400120r
    日期:2013.4.5
    The first copper-catalyzed N-arylation of 2-imidazolines is described. The reaction affords compounds with desirable lead-like characteristics in high yield with practical simplicity under inexpensive, "ligand-free" conditions. The cross coupling was successful with electron-rich and electron-poor aromatic iodides. Substrates bearing halides, esters, nitriles, and free hydroxyls are well tolerated, providing reactive handles for further functionalization, as are pyridines. In addition, the regioselective N-arylation of a 4-substituted imidazoline is reported.
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