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2,4-diamino-7-nitro-5-(4-methylphenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile | 1373941-23-1

中文名称
——
中文别名
——
英文名称
2,4-diamino-7-nitro-5-(4-methylphenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile
英文别名
——
2,4-diamino-7-nitro-5-(4-methylphenylsulfanyl)-5H-chromeno[2,3-b]pyridine-3-carbonitrile化学式
CAS
1373941-23-1
化学式
C20H15N5O3S
mdl
——
分子量
405.437
InChiKey
ARARLRPVJKWNFL-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

反应信息

  • 作为产物:
    描述:
    5-硝基水杨醛4-甲苯硫酚丙二腈potassium carbonate 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以65%的产率得到2,4-diamino-7-nitro-5-(4-methylphenylsulfanyl)-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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