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N3,7,7-trimethyl-1-(4-methoxyphenyl)-2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamide | 356579-87-8

中文名称
——
中文别名
——
英文名称
N3,7,7-trimethyl-1-(4-methoxyphenyl)-2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamide
英文别名
1-(4-Methoxyphenyl)-N,7,7-trimethyl-2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamide;1-(4-methoxyphenyl)-N,7,7-trimethyl-2,5-dioxo-6,8-dihydroquinoline-3-carboxamide
N3,7,7-trimethyl-1-(4-methoxyphenyl)-2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamide化学式
CAS
356579-87-8
化学式
C20H22N2O4
mdl
MFCD02905363
分子量
354.406
InChiKey
UMARLINSOBYXMZ-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):
    2.6
  • 重原子数:
    26
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    75.7
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    甲氧苯胺溶剂黄146 作用下, 以77%的产率得到N3,7,7-trimethyl-1-(4-methoxyphenyl)-2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamide
    参考文献:
    名称:
    An efficient synthesis of N1-substituted 2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamide via enolate salts
    摘要:
    Various 2-(2-cyano-2-carbamoyl-1-ethenyl)-5,5-dimethyl-3-oxo-1-cyclohexen-1-olates substituted in the amide group with dialkylammonium or sodium cations were prepared via reactions of N-substituted cyanoacetamides with dimedone-DMFDMA adduct by a one-pot, two-step protocol. The salts obtained were used in reactions with N-nucleophiles for further synthesis of the N1-substituted 2,5-dioxo- 1,2,5,6,7,8-hexahydro-3-quinolinecarboxamides that are analogues of well-known pharmaceuticals. The structure of the salts and the N1-substituted 2,5-dioxo-1,2,5,6,7,8-hexahydro-3-quinolinecarboxamides was established by means of spectroscopic and X-ray diffraction studies. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2008.02.095
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