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2-{5-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(pyridine-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine | 1399035-85-8

中文名称
——
中文别名
——
英文名称
2-{5-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(pyridine-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine
英文别名
2-[5-[4-fluoro-3-(trifluoromethyl)phenyl]-2-pyridin-4-ylimidazol-1-yl]-N,N-dimethylethanamine
2-{5-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(pyridine-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine化学式
CAS
1399035-85-8
化学式
C19H18F4N4
mdl
——
分子量
378.372
InChiKey
MNMHPHSDHRUZAG-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):
    3.2
  • 重原子数:
    27
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    34
  • 氢给体数:
    0
  • 氢受体数:
    7

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-{5-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(pyridine-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine盐酸platinum(IV) oxide氢气 作用下, 以 乙醇 为溶剂, 70.0 ℃ 、965.29 kPa 条件下, 反应 24.0h, 以64%的产率得到2-{5-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(piperidin-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine
    参考文献:
    名称:
    A Practical Synthesis of 2-{4-[4-Fluoro-3-(trifluoromethyl)phenyl]-2-(piperidin-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine
    摘要:
    A practical synthesis of the title compound was accomplished by hydrogenation of 2-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(pyridin-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine. The latter was obtained by N-alkylation of 4-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}pyridine. Treatment of N-{2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl}isonicotinamide hydrochloride with ammonium acetate in acetic acid provided 4-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}pyridine. Coupling of 2-amino-1-[4-fluoro-3-(trifluoromethyl)phenyl]ethanone 4-methylbenzene sulfonate with pyridine 4-carboxylic acid using either T3P or EDCI-HOBt provided N-{2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl}isonicotinamide hydrochloride.
    DOI:
    10.1055/s-0031-1290371
  • 作为产物:
    参考文献:
    名称:
    A Practical Synthesis of 2-{4-[4-Fluoro-3-(trifluoromethyl)phenyl]-2-(piperidin-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine
    摘要:
    A practical synthesis of the title compound was accomplished by hydrogenation of 2-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-2-(pyridin-4-yl)-1H-imidazol-1-yl}-N,N-dimethylethanamine. The latter was obtained by N-alkylation of 4-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}pyridine. Treatment of N-{2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl}isonicotinamide hydrochloride with ammonium acetate in acetic acid provided 4-{4-[4-fluoro-3-(trifluoromethyl)phenyl]-1H-imidazol-2-yl}pyridine. Coupling of 2-amino-1-[4-fluoro-3-(trifluoromethyl)phenyl]ethanone 4-methylbenzene sulfonate with pyridine 4-carboxylic acid using either T3P or EDCI-HOBt provided N-{2-[4-fluoro-3-(trifluoromethyl)phenyl]-2-oxoethyl}isonicotinamide hydrochloride.
    DOI:
    10.1055/s-0031-1290371
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