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4-(2-acetylphenylamino)-9-methylacridine-1,2-dione

中文名称
——
中文别名
——
英文名称
4-(2-acetylphenylamino)-9-methylacridine-1,2-dione
英文别名
TBBH;4-(2-Acetylanilino)-9-methylacridine-1,2-dione
4-(2-acetylphenylamino)-9-methylacridine-1,2-dione化学式
CAS
——
化学式
C22H16N2O3
mdl
——
分子量
356.381
InChiKey
DQXXAMJODKETAX-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):
    3.7
  • 重原子数:
    27
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    76.1
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    4-(2-acetylphenylamino)-9-methylacridine-1,2-dione三氟化硼乙醚 作用下, 以 二氯甲烷 为溶剂, 反应 24.0h, 以70%的产率得到5,8-Dimethyl-dibenzo[b,j][1,10]phenanthroline-6,7-dione
    参考文献:
    名称:
    Biomimetic synthesis of pyrido [2,3,4-kl]acridines
    摘要:
    A short new biomimetic route to the pyrido[2,3,4-kl]acridine ring system has been developed from readily available benzoquinone, or hydroquinone precursors, and beta,beta'-diaminoketones like kynuramine (3) or 2,2'-diaminobenzophenone (4), involving one key step. Pyrido[2,3,4-kl]acridine and closely related compounds have been prepared (5-9). The reaction has been shown to proceed to the formation of 1:1 and/or 1:2 quinone/amine adducts. Using of o-aminoacetophenone afforded dibenzo[1,10]phenanthrolinedione (11) a potential intermediate to eilatin 2.
    DOI:
    10.1016/s0040-4039(00)60789-x
  • 作为产物:
    描述:
    邻氨基苯乙酮邻苯二酚sodium iodate 作用下, 以 乙醇 为溶剂, 反应 30.0h, 以32.58%的产率得到4-(2-acetylphenylamino)-9-methylacridine-1,2-dione
    参考文献:
    名称:
    Aggregation-induced emission enhancement of polycyclic aromatic alkaloid derivatives and the crucial role of excited-state proton-transfer
    摘要:
    由于激发态的构型变化,在多环芳香生物碱衍生物中观察到聚集诱导发射增强(AIEE)现象,这归因于分子内质子转移和烯醇形式新结构的形成。
    DOI:
    10.1039/c0cc04827e
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文献信息

  • Biomimetic synthesis of pyrido [2,3,4-kl]acridines
    作者:Gari Gellerman、Amira Rudi、Yoel Kashman
    DOI:10.1016/s0040-4039(00)60789-x
    日期:1993.3
    A short new biomimetic route to the pyrido[2,3,4-kl]acridine ring system has been developed from readily available benzoquinone, or hydroquinone precursors, and beta,beta'-diaminoketones like kynuramine (3) or 2,2'-diaminobenzophenone (4), involving one key step. Pyrido[2,3,4-kl]acridine and closely related compounds have been prepared (5-9). The reaction has been shown to proceed to the formation of 1:1 and/or 1:2 quinone/amine adducts. Using of o-aminoacetophenone afforded dibenzo[1,10]phenanthrolinedione (11) a potential intermediate to eilatin 2.
  • Aggregation-induced emission enhancement of polycyclic aromatic alkaloid derivatives and the crucial role of excited-state proton-transfer
    作者:Tao He、XuTang Tao、JiaXiang Yang、Dan Guo、HaiBing Xia、Jiong Jia、MinHua Jiang
    DOI:10.1039/c0cc04827e
    日期:——
    Aggregation-induced emission enhancement (AIEE) phenomenon is observed in the polycyclic aromatic alkaloid derivatives due to the configuration changes in the excited state, which is attributed to intramolecular proton-transfer and the formation of a new structure of enol form.
    由于激发态的构型变化,在多环芳香生物碱衍生物中观察到聚集诱导发射增强(AIEE)现象,这归因于分子内质子转移和烯醇形式新结构的形成。
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