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6-amino-7-phenyl-[1,3]dioxo[4,5-g]quinoline 5-oxide | 1393939-20-2

中文名称
——
中文别名
——
英文名称
6-amino-7-phenyl-[1,3]dioxo[4,5-g]quinoline 5-oxide
英文别名
——
6-amino-7-phenyl-[1,3]dioxo[4,5-g]quinoline 5-oxide化学式
CAS
1393939-20-2
化学式
C16H12N2O3
mdl
——
分子量
280.283
InChiKey
AWIQXFAMVSNYHP-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:
    tin(II) chloride dihdyrate盐酸 作用下, 以 乙醇 为溶剂, 以71%的产率得到6-amino-7-phenyl-[1,3]dioxo[4,5-g]quinoline 5-oxide
    参考文献:
    名称:
    Novel and efficient synthesis of substituted quinoline-1-oxides and the complex compounds SnL2Cl2 (L=2-aminoquinoline-1-oxides) with the aid of stannous chloride
    摘要:
    A novel and efficient approach to the synthesis of substituted quinoline-1-oxides and the complex compounds SnL2Cl2 (L=2-aminoquinoline-1-oxides) was developed. The reaction has fancy selectivity when 3-(2-nitrophenyl)acrylonitriles were treated with the aid of SnCl2 reagent under the same conditions. When R is -CN or -COOR' the complex compounds SnL2Cl2 (L=2-aminoquinoline-1-oxides) were obtained. Whereas, when R is H or aryl another series of substituted quinoline-1-oxides were formed. The products have been screened for their anticancer activities. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2012.07.049
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