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4-(2-Fluoro-4-(trifluoromethyl)phenyl)piperidine | 1004852-72-5

中文名称
——
中文别名
——
英文名称
4-(2-Fluoro-4-(trifluoromethyl)phenyl)piperidine
英文别名
4-[2-fluoro-4-(trifluoromethyl)phenyl]piperidine
4-(2-Fluoro-4-(trifluoromethyl)phenyl)piperidine化学式
CAS
1004852-72-5
化学式
C12H13F4N
mdl
——
分子量
247.236
InChiKey
ZOVVKZZPQMXWED-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
  • 重原子数:
    17
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    12
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    1-甲基-1H-咪唑并[4,5-b]吡啶-2-甲醛盐酸盐4-(2-Fluoro-4-(trifluoromethyl)phenyl)piperidine 在 magnesium sulfate 、 三乙胺三乙酰氧基硼氢化钠 作用下, 以 二氯甲烷 为溶剂, 生成 2-((4-(2-fluoro-4-(trifluoromethyl)phenyl)piperidin-1-yl)methyl)-1-methyl-1H-imidazo[4,5-b]pyridine
    参考文献:
    名称:
    1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis
    摘要:
    A novel series of mGluR2 positive allosteric modulators (PAMs), 1-[(1-methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines, is herein disclosed. Structure-activity relationship studies led to potent, selective mGluR2 PAMs with excellent pharmacokinetic profiles. A representative lead compound (+)-17e demonstrated dose-dependent inhibition of methamphetamine-induced hyperactivity and mescaline-induced scratching in mice, providing support for potential efficacy in treating psychosis.
    DOI:
    10.1021/jm101414h
  • 作为产物:
    描述:
    2-氟-4-(三氟甲基)苯硼酸platinum(IV) oxide四(三苯基膦)钯氢气碳酸氢钠 作用下, 以 甲醇乙二醇二甲醚 为溶剂, 20.0~85.0 ℃ 、275.8 kPa 条件下, 生成 4-(2-Fluoro-4-(trifluoromethyl)phenyl)piperidine
    参考文献:
    名称:
    1-[(1-Methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis
    摘要:
    A novel series of mGluR2 positive allosteric modulators (PAMs), 1-[(1-methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines, is herein disclosed. Structure-activity relationship studies led to potent, selective mGluR2 PAMs with excellent pharmacokinetic profiles. A representative lead compound (+)-17e demonstrated dose-dependent inhibition of methamphetamine-induced hyperactivity and mescaline-induced scratching in mice, providing support for potential efficacy in treating psychosis.
    DOI:
    10.1021/jm101414h
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文献信息

  • 1-[(1-Methyl-1<i>H</i>-imidazol-2-yl)methyl]-4-phenylpiperidines as mGluR2 Positive Allosteric Modulators for the Treatment of Psychosis
    作者:Lei Zhang、Michael A. Brodney、John Candler、Angela C. Doran、Allen J. Duplantier、Ivan V. Efremov、Edel Evrard、Kenneth Kraus、Alan H. Ganong、Jessica A. Haas、Ashley N. Hanks、Keith Jenza、John T. Lazzaro、Noha Maklad、Sheryl A. McCarthy、Weimin Qian、Bruce N. Rogers、Melinda D. Rottas、Christopher J. Schmidt、Judith A. Siuciak、F. David Tingley、Andy Q. Zhang
    DOI:10.1021/jm101414h
    日期:2011.3.24
    A novel series of mGluR2 positive allosteric modulators (PAMs), 1-[(1-methyl-1H-imidazol-2-yl)methyl]-4-phenylpiperidines, is herein disclosed. Structure-activity relationship studies led to potent, selective mGluR2 PAMs with excellent pharmacokinetic profiles. A representative lead compound (+)-17e demonstrated dose-dependent inhibition of methamphetamine-induced hyperactivity and mescaline-induced scratching in mice, providing support for potential efficacy in treating psychosis.
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