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(E)-1-(2-chloro-5-(3-(methylamino)-3-oxo-1-phenylprop-1-en-1-yl)pyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide | 231618-73-8

中文名称
——
中文别名
——
英文名称
(E)-1-(2-chloro-5-(3-(methylamino)-3-oxo-1-phenylprop-1-en-1-yl)pyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide
英文别名
——
(E)-1-(2-chloro-5-(3-(methylamino)-3-oxo-1-phenylprop-1-en-1-yl)pyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-ide化学式
CAS
231618-73-8
化学式
C23H19ClN2O2
mdl
——
分子量
390.869
InChiKey
HHDVPFRLTMWVAY-XSFVSMFZSA-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):
    None
  • 重原子数:
    None
  • 可旋转键数:
    None
  • 环数:
    None
  • sp3杂化的碳原子比例:
    None
  • 拓扑面积:
    None
  • 氢给体数:
    None
  • 氢受体数:
    None

反应信息

  • 作为反应物:
    描述:
    氰胺(E)-1-(2-chloro-5-(3-(methylamino)-3-oxo-1-phenylprop-1-en-1-yl)pyridin-1-ium-1-yl)-2-oxo-2-phenylethan-1-idepotassium carbonate 作用下, 以 乙腈 为溶剂, 以40%的产率得到(E)-3-(2-amino-3-benzoylimidazo[1,2-a]pyridin-6-yl)-N-methyl-3-phenylprop-2-enamide
    参考文献:
    名称:
    Short synthesis and anti-rhinoviral activity of imidazo[1,2-a]pyridines: The effect of acyl groups at 3-position
    摘要:
    Various 2-amino-3-acyl-6-[(E)-1-phenyl-2-N-methylcarbamoylvinyl]-imidazo[1,2-a]pyridines, structurally related to Enviroxime were prepared to determine the effect of acyl groups on the anti-rhinoviral activity. A short and efficient means for the construction of the imidazo nucleus as well as biological evaluation of the final compounds are disclosed. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00193-6
  • 作为产物:
    参考文献:
    名称:
    Short synthesis and anti-rhinoviral activity of imidazo[1,2-a]pyridines: The effect of acyl groups at 3-position
    摘要:
    Various 2-amino-3-acyl-6-[(E)-1-phenyl-2-N-methylcarbamoylvinyl]-imidazo[1,2-a]pyridines, structurally related to Enviroxime were prepared to determine the effect of acyl groups on the anti-rhinoviral activity. A short and efficient means for the construction of the imidazo nucleus as well as biological evaluation of the final compounds are disclosed. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(99)00193-6
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相关结构分类