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2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propen-1-yl) acrylamide | 228562-22-9

中文名称
——
中文别名
——
英文名称
2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propen-1-yl) acrylamide
英文别名
2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propene-1-yl)acrylamide;2-[(3-chlorophenyl)methylidene]-3-oxo-N-(3-phenylprop-2-enyl)butanamide
2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propen-1-yl) acrylamide化学式
CAS
228562-22-9
化学式
C20H18ClNO2
mdl
——
分子量
339.821
InChiKey
NZVHFSCGIHNXQU-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):
    4.7
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    46.2
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propen-1-yl) acrylamidesodium acetate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 4-(3-chlorophenyl)-6-methyl-2-(methylthio)-N-(3-phenyl-2-propen-1-yl)-5-pyrimidinecarboxamide
    参考文献:
    名称:
    NOVEL PYRIMIDINE DERIVATIVE AND NOVEL PYRIDINE DERIVATIVE
    摘要:
    非手性嘧啶衍生物和以下结构式或其类似物的吡啶衍生物具有选择性N型钙通道拮抗活性,并且当口服时表现出镇痛作用。它们可用作与N型钙通道相关的疼痛和各种疾病的治疗药物。
    公开号:
    EP1318147A1
  • 作为产物:
    描述:
    3-oxo-N-(3-phenyl-2-propen-1-yl) butylamide3-氯苯甲醛哌啶溶剂黄146 作用下, 以 异丙醇 为溶剂, 反应 48.0h, 以88%的产率得到2-acetyl-3-(3-chlorophenyl)-N-(3-phenyl-2-propen-1-yl) acrylamide
    参考文献:
    名称:
    Pyrimidine derivatives and new pyridine derivatives
    摘要:
    Achirai嘧啶衍生物和以下结构式或其类似物的吡啶衍生物具有选择性N型钙通道拮抗活性,并在口服时显示镇痛作用。它们可用作与N型钙通道相关的疼痛和各种疾病的治疗药物。
    公开号:
    US20040009991A1
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文献信息

  • NEW PYRIMIDINE DERIVATIVES AND NEW PYRIDINE DERIVATIVES
    申请人:OHNO Seiji
    公开号:US20080070903A1
    公开(公告)日:2008-03-20
    Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when they were taken orally. They are useful as therapeutic agents for pains and various diseases associated with the N-type calcium channels.
    以下式子或其类似物的非手性嘧啶生物吡啶衍生物具有选择性N型通道拮抗活性,并且口服时表现出镇痛作用。它们可用作治疗与N型通道相关的疼痛和各种疾病的治疗剂。
  • Pyrimidine compounds useful as N-type calcium channel antagonists
    申请人:Ajinomoto Co., Inc.
    公开号:US07288544B2
    公开(公告)日:2007-10-30
    Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when they were taken orally. They are useful as therapeutic agents for pains and various diseases associated with the N-type calcium channels
    以下式子或其类似物的无手性嘧啶生物吡啶衍生物具有选择性N型通道拮抗活性,并且口服时表现出镇痛作用。它们可用作治疗与N型通道相关的疼痛和各种疾病的治疗剂。
  • Dihydropyridine derivative
    申请人:Ajinomoto Co., Inc.
    公开号:US06350762B1
    公开(公告)日:2002-02-26
    Dihydropyridine derivatives of the following formula, analogs thereof and pharmaceutically acceptable salts thereof have an activity of selectively inhibiting the action of N-type calcium channel. They are used as remedies for various diseases relating to the N-type calcium channel.
    以下公式的二氢吡啶衍生物,其类似物和药学上可接受的盐具有选择性抑制N型通道作用的活性。它们被用作治疗与N型通道相关的各种疾病的药物。
  • Pyridine compounds useful as N-type calcium channel antagonists
    申请人:Ajinomoto Co., Inc.
    公开号:US07494989B2
    公开(公告)日:2009-02-24
    Achiral pyrimidine derivatives and pyridine derivatives of the following formulae or analogs thereof have selective N-type calcium channel antagonistic activity and showed analgesic action when they were taken orally. They are useful as therapeutic agents for pains and various diseases associated with the N-type calcium channels.
    以下公式或其类似物的无手性嘧啶生物吡啶衍生物具有选择性N型通道拮抗活性,并在口服时显示镇痛作用。它们可用作治疗与N型通道相关的疼痛和各种疾病的治疗剂。
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