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1-[2-(4-ethoxycarbonylpiperazin-1-yl)acetyl]-3-ethyl-2,6-bis(p-fluorophenyl)piperidin-4-one | 1282624-16-1

中文名称
——
中文别名
——
英文名称
1-[2-(4-ethoxycarbonylpiperazin-1-yl)acetyl]-3-ethyl-2,6-bis(p-fluorophenyl)piperidin-4-one
英文别名
Ethyl 4-[2-[3-ethyl-2,6-bis(4-fluorophenyl)-4-oxo-1-piperidyl]-2-oxo-ethyl]piperazine-1-carboxylate;ethyl 4-[2-[3-ethyl-2,6-bis(4-fluorophenyl)-4-oxopiperidin-1-yl]-2-oxoethyl]piperazine-1-carboxylate
1-[2-(4-ethoxycarbonylpiperazin-1-yl)acetyl]-3-ethyl-2,6-bis(p-fluorophenyl)piperidin-4-one化学式
CAS
1282624-16-1
化学式
C28H33F2N3O4
mdl
——
分子量
513.585
InChiKey
FKPPVRUKGKRVIO-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):
    3.5
  • 重原子数:
    37
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    70.2
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    3-ethyl-2,6-bis(4-fluorophenyl)piperidin-4-one 在 三乙胺 作用下, 以 甲苯 为溶剂, 生成 1-[2-(4-ethoxycarbonylpiperazin-1-yl)acetyl]-3-ethyl-2,6-bis(p-fluorophenyl)piperidin-4-one
    参考文献:
    名称:
    Design and synthesis of novel piperazine unit condensed 2,6-diarylpiperidin-4-one derivatives as antituberculosis and antimicrobial agents
    摘要:
    A new series of 1-[2-(4-ethoxycarbonylpiperazine-1-yl)acetyl]-2,6-diarylpiperidin-4-ones (3a-3j) has been synthesized by conventional method and were characterized by IR, elemental analysis, mass spectral, 1 H NMR, C-13 NMR, and single crystal X-ray diffraction analysis. The synthesized compounds were evaluated for their antituberculosis activity against Mycobacterium tuberculosis H37Rv (ATCC-27294) and also its antimicrobial activity were examined against five familiar bacterial and fungal strains. Among the synthesized compounds, compounds 3e-3j exhibit higher inhibition potency (16 mu g/ml) against M. tuberculosis H37Rv. Furthermore, compounds containing fluoro substituent in the phenyl ring at C-2 and C-6 positions of the piperidin-4-one motif (compounds 3c, 3d, and 3i) exerted better antibacterial and antifungal activity than the other phenyl-substituted compounds.
    DOI:
    10.1007/s00044-011-9573-9
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文献信息

  • Design and synthesis of novel piperazine unit condensed 2,6-diarylpiperidin-4-one derivatives as antituberculosis and antimicrobial agents
    作者:Mannangatty Rani、Paramasivam Parthiban、Rajamanickam Ramachandran、Senthamaraikannan Kabilan
    DOI:10.1007/s00044-011-9573-9
    日期:2012.5
    A new series of 1-[2-(4-ethoxycarbonylpiperazine-1-yl)acetyl]-2,6-diarylpiperidin-4-ones (3a-3j) has been synthesized by conventional method and were characterized by IR, elemental analysis, mass spectral, 1 H NMR, C-13 NMR, and single crystal X-ray diffraction analysis. The synthesized compounds were evaluated for their antituberculosis activity against Mycobacterium tuberculosis H37Rv (ATCC-27294) and also its antimicrobial activity were examined against five familiar bacterial and fungal strains. Among the synthesized compounds, compounds 3e-3j exhibit higher inhibition potency (16 mu g/ml) against M. tuberculosis H37Rv. Furthermore, compounds containing fluoro substituent in the phenyl ring at C-2 and C-6 positions of the piperidin-4-one motif (compounds 3c, 3d, and 3i) exerted better antibacterial and antifungal activity than the other phenyl-substituted compounds.
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