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1,8-bis(4-oxo-1,3-diphenylimidazo[1,5-a]quinoxalin-5-yl)-3,5-dioxapentane | 1123811-99-3

中文名称
——
中文别名
——
英文名称
1,8-bis(4-oxo-1,3-diphenylimidazo[1,5-a]quinoxalin-5-yl)-3,5-dioxapentane
英文别名
1,8-bis(1,3-diphenylimidazo[1,5-a]quinoxalin-4-on-5-yl)-3,6-dioxaoctane
1,8-bis(4-oxo-1,3-diphenylimidazo[1,5-a]quinoxalin-5-yl)-3,5-dioxapentane化学式
CAS
1123811-99-3
化学式
C50H40N6O4
mdl
——
分子量
788.905
InChiKey
HJHMIMCHWMGWND-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:
    1,1'-(3,6-Dioxaoctane-1,8-diyl)bis[3-benzoyl-quinoxalin-2(1h)-one] 、 苄胺二甲基亚砜 为溶剂, 以60%的产率得到1,8-bis(4-oxo-1,3-diphenylimidazo[1,5-a]quinoxalin-5-yl)-3,5-dioxapentane
    参考文献:
    名称:
    An efficient method for the synthesis of imidazo[1,5-a]quinoxalines from 3-acylquinoxalinones and benzylamines via a novel imidazoannulation
    摘要:
    The reaction of 3-aroylquinoxalin-2(1H)-ones and their N-alkyl analogues with benzylamines in DMSO proceeds through an intermediate formation of N-(alpha-quinoxalinylbenzylydene)benzylamine, which when subjected to oxidative cyclocondensation gives imidazo[1,5-a]quinoxalines. Applying this new approach of imidazoannullation to the bis-3-aroylquinoxalines makes it possible to develop fundamentally new methods of the synthesis of bis-imidazo[1,5-a]quinoxalines with the use of different benzylamines and heteromacrocycles with the 1,3-bis(3-arylimidazo[1,5-a]quinoxalin-1-yl)benzene structural fragment when m-xylylenediamine is used. (c) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tet.2009.08.081
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文献信息

  • Polyfused nitrogen heterocycles: XIX. Oxidative imidazo-fusion of 3-benzoylquinoxalin-2-ones with benzylamines in the synthesis of bis(imidazo[1,5-a]quinoxalin-1- and -5-yl) derivatives
    作者:A. A. Kalinin、V. A. Mamedov
    DOI:10.1134/s1070428008050187
    日期:2008.5
    Oxidative cyclocondensation of bis(3-benzoylquinoxalin-1-yl)alkanes and oxaalkanes with benzylamine and 3-benzoylquinoxalinones with m-xylylenediamine proceeded with the formation of bis-(imidazo[1,5-a]quinoxalinyl) derivatives where the hetaryl fragments were linked by a spacer both through the imidazole and quinoxaline fragments.
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