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2,3-dipyridin-2-yl-1,4,5,12-tetraazatriphenylene | 7756-04-9

中文名称
——
中文别名
——
英文名称
2,3-dipyridin-2-yl-1,4,5,12-tetraazatriphenylene
英文别名
2,3-di-pyridin-2-yl-pyrazino[2,3-f][4,7]phenanthroline;2,3-Bis-(2)-pyridyl-dipyrido<2,3-f:3',2'-h>-chinoxalin;2,3-Dipyridin-2-ylpyrazino[2,3-f][4,7]phenanthroline;2,3-dipyridin-2-ylpyrazino[2,3-f][4,7]phenanthroline
2,3-dipyridin-2-yl-1,4,5,12-tetraazatriphenylene化学式
CAS
7756-04-9
化学式
C24H14N6
mdl
——
分子量
386.415
InChiKey
TYERBOSRLSZOAB-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

物化性质

  • 熔点:
    >360 °C
  • 沸点:
    616.0±50.0 °C(Predicted)
  • 密度:
    1.371±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3
  • 重原子数:
    30
  • 可旋转键数:
    2
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    77.3
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    泛喹酮 在 palladium on activated charcoal 盐酸羟胺一水合肼barium carbonate 作用下, 以 乙醇 为溶剂, 反应 23.0h, 生成 2,3-dipyridin-2-yl-1,4,5,12-tetraazatriphenylene
    参考文献:
    名称:
    Efficient Synthesis of 1,4,5,12-Tetraazatriphenylene and Derivatives
    摘要:
    Condensation of 5,6-diamino-4,7-phenanthroline with glyoxal provides 1,4,5,12-tetraazatriphenylene in quantitative yield. This procedure avoids the 50% loss of product inherent in previous methods. Derivatives were also prepared by using alpha-dicarbonyl compounds other than glyoxal. Additional derivatives were prepared from 1,4,5,12-tetraazatriphenylene-2,3-dicarbonitrile, produced by condensation of diaminomaleonitrile with 4,7-phenanthroline-5,6-dione.
    DOI:
    10.1021/jo0495283
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文献信息

  • Efficient Synthesis of 1,4,5,12-Tetraazatriphenylene and Derivatives
    作者:Chandima Abeywickrama、Arthur David Baker
    DOI:10.1021/jo0495283
    日期:2004.10.1
    Condensation of 5,6-diamino-4,7-phenanthroline with glyoxal provides 1,4,5,12-tetraazatriphenylene in quantitative yield. This procedure avoids the 50% loss of product inherent in previous methods. Derivatives were also prepared by using alpha-dicarbonyl compounds other than glyoxal. Additional derivatives were prepared from 1,4,5,12-tetraazatriphenylene-2,3-dicarbonitrile, produced by condensation of diaminomaleonitrile with 4,7-phenanthroline-5,6-dione.
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