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4-octyl-4,6-dihydro-3H-pyrano[3,2-c]quinoline-2,5-dione | 1448786-41-1

中文名称
——
中文别名
——
英文名称
4-octyl-4,6-dihydro-3H-pyrano[3,2-c]quinoline-2,5-dione
英文别名
——
4-octyl-4,6-dihydro-3H-pyrano[3,2-c]quinoline-2,5-dione化学式
CAS
1448786-41-1
化学式
C20H25NO3
mdl
——
分子量
327.423
InChiKey
DTLTVGJAYZZJHJ-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):
    4.9
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    55.4
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    丙二酸环(亚)异丙酯壬醛2,4-喹啉二醇1-甲基-3-丁基咪唑硫酸氢盐 作用下, 反应 1.33h, 以74%的产率得到4-octyl-4,6-dihydro-3H-pyrano[3,2-c]quinoline-2,5-dione
    参考文献:
    名称:
    Synthesis of novel pyrano[3,2-c]quinoline-2,5-diones using an acidic ionic liquid catalyst
    摘要:
    The synthesis of novel 4-substituted-3,4-dihydro-6H-pyrano[3,2-c]quinoline-2,5-diones was accomplished efficiently via a three-component reaction between 4-hydroxyquinoline-2-one, Meldrum's acid, and an alkyl or arylaldehyde under catalysis by [Bmim]HSO4. The ionic liquid catalyst offers the advantage of realizing the synthesis of the title products at ambient temperature and widens the scope of the reactants to include aliphatic aldehydes with respect to the catalysts already applied for similar syntheses. (C) 2013 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2013.06.050
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文献信息

  • Synthesis of novel pyrano[3,2-c]quinoline-2,5-diones using an acidic ionic liquid catalyst
    作者:Kurosh Rad-Moghadam、Seyyedeh Cobra Azimi、Esmayeel Abbaspour-Gilandeh
    DOI:10.1016/j.tetlet.2013.06.050
    日期:2013.8
    The synthesis of novel 4-substituted-3,4-dihydro-6H-pyrano[3,2-c]quinoline-2,5-diones was accomplished efficiently via a three-component reaction between 4-hydroxyquinoline-2-one, Meldrum's acid, and an alkyl or arylaldehyde under catalysis by [Bmim]HSO4. The ionic liquid catalyst offers the advantage of realizing the synthesis of the title products at ambient temperature and widens the scope of the reactants to include aliphatic aldehydes with respect to the catalysts already applied for similar syntheses. (C) 2013 Elsevier Ltd. All rights reserved.
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