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3-(4-chlorophenyl)-9-methoxy-1-phenyl-5H-chromeno[3,4-b]pyridin-5-one | 1414381-95-5

中文名称
——
中文别名
——
英文名称
3-(4-chlorophenyl)-9-methoxy-1-phenyl-5H-chromeno[3,4-b]pyridin-5-one
英文别名
3-(4-Chlorophenyl)-9-methoxy-1-phenylchromeno[3,4-b]pyridin-5-one;3-(4-chlorophenyl)-9-methoxy-1-phenylchromeno[3,4-b]pyridin-5-one
3-(4-chlorophenyl)-9-methoxy-1-phenyl-5H-chromeno[3,4-b]pyridin-5-one化学式
CAS
1414381-95-5
化学式
C25H16ClNO3
mdl
——
分子量
413.86
InChiKey
BRDBXKLMOQWTJY-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):
    6.2
  • 重原子数:
    30
  • 可旋转键数:
    3
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    48.4
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    4-氯苯甲醛6-methoxy-3-aminocoumarin苯乙炔 作用下, 以 乙腈 为溶剂, 反应 2.0h, 以78%的产率得到3-(4-chlorophenyl)-9-methoxy-1-phenyl-5H-chromeno[3,4-b]pyridin-5-one
    参考文献:
    名称:
    A simple and expedient synthesis of functionalized pyrido[2,3-c] coumarin derivatives using molecular iodine catalyzed three-component reaction
    摘要:
    A wide variety of substituted pyrido[2,3-c] coumarin derivatives have been accomplished from 3-aminocoumarins, aromatic aldehydes, and alkynes in the presence of 10 mol % molecular iodine in acetonitrile under reflux conditions through one-pot Povarov reactions. Good yields, no need of aqueous work-up procedure and chromatographic separation, environmentally benign are some of the salient features of the present protocol. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.09.051
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文献信息

  • A simple and expedient synthesis of functionalized pyrido[2,3-c] coumarin derivatives using molecular iodine catalyzed three-component reaction
    作者:Abu T. Khan、Deb K. Das、Kobirul Islam、Pradipta Das
    DOI:10.1016/j.tetlet.2012.09.051
    日期:2012.11
    A wide variety of substituted pyrido[2,3-c] coumarin derivatives have been accomplished from 3-aminocoumarins, aromatic aldehydes, and alkynes in the presence of 10 mol % molecular iodine in acetonitrile under reflux conditions through one-pot Povarov reactions. Good yields, no need of aqueous work-up procedure and chromatographic separation, environmentally benign are some of the salient features of the present protocol. (C) 2012 Elsevier Ltd. All rights reserved.
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