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11-(4-hydroxy-2-oxo-1H-quinolin-3-yl)-1,3,8,8-tetramethyl-6-(4-methylphenyl)-9,11-dihydro-7H-quinolino[2,3-b]quinolin-10-one | 1591873-48-1

中文名称
——
中文别名
——
英文名称
11-(4-hydroxy-2-oxo-1H-quinolin-3-yl)-1,3,8,8-tetramethyl-6-(4-methylphenyl)-9,11-dihydro-7H-quinolino[2,3-b]quinolin-10-one
英文别名
——
11-(4-hydroxy-2-oxo-1H-quinolin-3-yl)-1,3,8,8-tetramethyl-6-(4-methylphenyl)-9,11-dihydro-7H-quinolino[2,3-b]quinolin-10-one化学式
CAS
1591873-48-1
化学式
C36H33N3O3
mdl
——
分子量
555.676
InChiKey
CPHFVGLGPNOCSB-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):
    6.6
  • 重原子数:
    42
  • 可旋转键数:
    2
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    82.5
  • 氢给体数:
    2
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    2-氯-5,7-二甲基-3-喹啉甲醛2,4-喹啉二醇5,5-二甲基-3-(4-甲基苯胺基)环己-2-烯-1-酮L-脯氨酸 作用下, 以 乙醇 为溶剂, 反应 8.0h, 以82%的产率得到11-(4-hydroxy-2-oxo-1H-quinolin-3-yl)-1,3,8,8-tetramethyl-6-(4-methylphenyl)-9,11-dihydro-7H-quinolino[2,3-b]quinolin-10-one
    参考文献:
    名称:
    Efficient Synthesis of Functionalized Benzo[b][1,8]naphthyridine Derivatives via Three-Component Reaction Catalyzed by l-Proline
    摘要:
    A facile and efficient one-pot procedure for the preparation of functionalized benzo[b][1,8]naphthyridine derivatives by three-component reaction of 2-chloroquinoline-3-carbaldehyde, 1,3-dicarbonyl compounds, and enaminones catalyzed by l-proline is described. This new protocol has the advantages of environmental friendliness, good yields, and convenient operation.
    DOI:
    10.1021/co4001524
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文献信息

  • Efficient Synthesis of Functionalized Benzo[<i>b</i>][1,8]naphthyridine Derivatives via Three-Component Reaction Catalyzed by <scp>l</scp>-Proline
    作者:Lei Fu、Wei Lin、Ming-Hua Hu、Xue-Cheng Liu、Zhi-Bin Huang、Da-Qing Shi
    DOI:10.1021/co4001524
    日期:2014.5.12
    A facile and efficient one-pot procedure for the preparation of functionalized benzo[b][1,8]naphthyridine derivatives by three-component reaction of 2-chloroquinoline-3-carbaldehyde, 1,3-dicarbonyl compounds, and enaminones catalyzed by l-proline is described. This new protocol has the advantages of environmental friendliness, good yields, and convenient operation.
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