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2,4-diamino-7-chloro-5-(phenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile | 1373941-25-3

中文名称
——
中文别名
——
英文名称
2,4-diamino-7-chloro-5-(phenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile
英文别名
2,4-diamino-7-chloro-5-phenylsulfanyl-5H-chromeno[2,3-b]pyridine-3-carbonitrile
2,4-diamino-7-chloro-5-(phenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile化学式
CAS
1373941-25-3
化学式
C19H13ClN4OS
mdl
——
分子量
380.857
InChiKey
VBNHIVSDQQDZFS-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):
    4.4
  • 重原子数:
    26
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    123
  • 氢给体数:
    2
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    苯硫酚5-氯代水杨醛丙二腈potassium carbonate 作用下, 以 乙醇 为溶剂, 反应 4.0h, 以70%的产率得到2,4-diamino-7-chloro-5-(phenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile
    参考文献:
    名称:
    K2CO3-Mediated, One-Pot, Multicomponent Synthesis of Medicinally Potent Pyridine and Chromeno[2,3-b]pyridine Scaffolds
    摘要:
    An efficient one-pot, multicomponent synthesis of 3,5-dicyanopyridines has been developed from the reaction of malononitrile and different thiophenol or thiols with a variety of aldehydes (aromatic including hindered ones, heteroaromatic, and aliphatic) in the presence of 20 mol% of K2CO3 in refluxing 50% aqeuous ethanol. KMnO4 has been utilized as a readily available, inexpensive oxidant for the in situ transformation of the initially formed dihydropyridine intermediate. K2CO3 also mediates the one-pot formation of chromeno[2,3-b]pyridines from reaction of salicylaldehyde or its analogs with malononitrile and thiol or thiophenols. Both of these conditions also work equally well under 50-fold scale-up conditions.Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.
    DOI:
    10.1080/00397911.2011.555284
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