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10-chloro-6-(2,4-dichlorophenyl)-1,2,5,6-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-4,7-dione | 1256151-07-1

中文名称
——
中文别名
——
英文名称
10-chloro-6-(2,4-dichlorophenyl)-1,2,5,6-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-4,7-dione
英文别名
4-Chloro-10-(2,4-dichlorophenyl)-1,13-diazatetracyclo[7.6.1.02,7.013,16]hexadeca-2(7),3,5,9(16)-tetraene-8,12-dione
10-chloro-6-(2,4-dichlorophenyl)-1,2,5,6-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-4,7-dione化学式
CAS
1256151-07-1
化学式
C20H13Cl3N2O2
mdl
——
分子量
419.694
InChiKey
VONFVXGWLUAXEO-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:
    27
  • 可旋转键数:
    1
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    40.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Modulating the Reactivity of Heterocyclic Ketene Aminals in MCR: Selective Construction of Tetrahydrobenzo[b]imidazo[3,2,1-ij][1,8]naphthyridines
    摘要:
    Two new kinds of tetrahydrobenzo[b]imidazo[3,2,1-iota j][1,8]naphthyndine derivatives have been successfully synthesized by cascade reactions including Knoevenagel condensation, aza-ene reaction, imine-enamine tautomenzation, cyclocondensation, and intramolecular SNAr of precursors 2-(2-chloroaroyl)methyleneimidazolidines with aromatic aldehydes and ethyl acetoacetate or Meldrum's acid under mild conditions, respectively These studies highlighted the concept of a substrate-design approach to the development of novel multicomponent reactions by simply incorporating an o-halo group into the aryl ring of 2-benzoyl-methyleneimidazolidine as new synthons In this domino reaction, at least six different active sites are involved, two C-C bonds, two C-N bonds, and two new rings are constructed with all reactants efficiently utilized in the chemical transformation
    DOI:
    10.1021/jo101454q
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