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(E)-3-(4-chlorophenyl)-N-[2-(pyrrolidin-1-ylmethyl)cyclohexyl]-prop-2-enamide

中文名称
——
中文别名
——
英文名称
(E)-3-(4-chlorophenyl)-N-[2-(pyrrolidin-1-ylmethyl)cyclohexyl]-prop-2-enamide
英文别名
(E)-3-(4-chlorophenyl)-N-[2-(pyrrolidin-1-ylmethyl)cyclohexyl]prop-2-enamide
(E)-3-(4-chlorophenyl)-N-[2-(pyrrolidin-1-ylmethyl)cyclohexyl]-prop-2-enamide化学式
CAS
——
化学式
C20H27ClN2O
mdl
——
分子量
346.9
InChiKey
AMJGYVGEGNYKQL-FMIVXFBMSA-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):
    4.5
  • 重原子数:
    24
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    32.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    (2E)-3-(4-氯苯基)丙烯酰氯 、 2-(Pyrrolidin-1-ylmethyl)cyclohexan-1-amine 以 为溶剂, 反应 0.75h, 以46%的产率得到(E)-3-(4-chlorophenyl)-N-[2-(pyrrolidin-1-ylmethyl)cyclohexyl]-prop-2-enamide
    参考文献:
    名称:
    Anti-inflammatory and Analgesic Amides: New Developments
    摘要:
    A series of substituted N-cycloalkyl benzamides, cinnamamides, and indole-3-carboxamides were synthesized and evaluated for their analgesic, antiinflammatory activities as well as for their gastrointestinal irritation liability. Indomethacin was used as reference drug in both tests. Compounds 1k, 1b, 1h, 1j, and 1g were the most active in the antiinflammatory paw edema inhibition test, with a sharply dose-dependent effect. In terms of the analgesic activity (acetic acid writhing test), the most active compound was 5a followed by 3a, but many other compounds were found to have a non-negligible potency. Even in this case, the effect was dose dependent.
    DOI:
    10.1002/(sici)1521-4184(200001)333:1<17::aid-ardp17>3.0.co;2-0
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文献信息

  • Anti-inflammatory and Analgesic Amides: New Developments
    作者:Michele Palomba、Amedeo Pau、Gianpiero Boatto、Battistina Asproni、Luciana Auzzas、Riccardo Cerri、Loredana Arenare、Walter Filippelli、Giuseppe Falcone、Giulia Motola
    DOI:10.1002/(sici)1521-4184(200001)333:1<17::aid-ardp17>3.0.co;2-0
    日期:2000.1
    A series of substituted N-cycloalkyl benzamides, cinnamamides, and indole-3-carboxamides were synthesized and evaluated for their analgesic, antiinflammatory activities as well as for their gastrointestinal irritation liability. Indomethacin was used as reference drug in both tests. Compounds 1k, 1b, 1h, 1j, and 1g were the most active in the antiinflammatory paw edema inhibition test, with a sharply dose-dependent effect. In terms of the analgesic activity (acetic acid writhing test), the most active compound was 5a followed by 3a, but many other compounds were found to have a non-negligible potency. Even in this case, the effect was dose dependent.
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