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7-methoxy-8-(pyridin-3-yl)-2H-chromen-2-one | 1358063-70-3

中文名称
——
中文别名
——
英文名称
7-methoxy-8-(pyridin-3-yl)-2H-chromen-2-one
英文别名
7-Methoxy-8-pyridin-3-ylchromen-2-one;7-methoxy-8-pyridin-3-ylchromen-2-one
7-methoxy-8-(pyridin-3-yl)-2H-chromen-2-one化学式
CAS
1358063-70-3
化学式
C15H11NO3
mdl
——
分子量
253.257
InChiKey
BOAXLGBYQHWDBJ-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):
    2.4
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.07
  • 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:
    2-iodo-3-methoxy-6-vinylphenol 在 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 、 bis-triphenylphosphine-palladium(II) chloride 、 caesium carbonate三乙胺 作用下, 以 1,4-二氧六环二氯甲烷甲苯 为溶剂, 反应 18.5h, 生成 7-methoxy-8-(pyridin-3-yl)-2H-chromen-2-one
    参考文献:
    名称:
    Synthesis of 8-Aryl-Substituted Coumarins Based on Ring-Closing Metathesis and Suzuki–Miyaura Coupling: Synthesis of a Furyl Coumarin Natural Product from Galipea panamensis
    摘要:
    The synthesis of 7-methoxy-8-(4-methyl-3-furyl)-2H-chromen-2-one, a natural product with antileishmanial activity recently isolated from the plant Galipea panamensis, is described. The key step is a Suzuki-Miyaura coupling of a furan-3-boronic acid and an 8-halocoumarin, which is advantageously synthesized using a ring-closing metathesis reaction. Several non-natural analogues are also available along these lines.
    DOI:
    10.1021/jo2026564
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文献信息

  • Synthesis of 8-Aryl-Substituted Coumarins Based on Ring-Closing Metathesis and Suzuki–Miyaura Coupling: Synthesis of a Furyl Coumarin Natural Product from <i>Galipea panamensis</i>
    作者:Bernd Schmidt、Stefan Krehl、Alexandra Kelling、Uwe Schilde
    DOI:10.1021/jo2026564
    日期:2012.3.2
    The synthesis of 7-methoxy-8-(4-methyl-3-furyl)-2H-chromen-2-one, a natural product with antileishmanial activity recently isolated from the plant Galipea panamensis, is described. The key step is a Suzuki-Miyaura coupling of a furan-3-boronic acid and an 8-halocoumarin, which is advantageously synthesized using a ring-closing metathesis reaction. Several non-natural analogues are also available along these lines.
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