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8-chloro-6H-indolo[2,3-b]quinoline | 1150313-13-5

中文名称
——
中文别名
——
英文名称
8-chloro-6H-indolo[2,3-b]quinoline
英文别名
——
8-chloro-6H-indolo[2,3-b]quinoline化学式
CAS
1150313-13-5
化学式
C15H9ClN2
mdl
——
分子量
252.703
InChiKey
LMWJAVBCVRKVMV-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

  • 沸点:
    496.4±25.0 °C(predicted)
  • 密度:
    1.441±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    28.7
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    6-chloro-3-(2-nitrobenzyl)-1H-indole三苯基膦 作用下, 以 二苯醚 为溶剂, 反应 5.0h, 以55%的产率得到8-chloro-6H-indolo[2,3-b]quinoline
    参考文献:
    名称:
    A Concise Synthesis of 6H-Indolo[2,3-b]quinolines: Formal Synthesis of Neocryptolepine
    摘要:
    A new two-step approach for the synthesis of 6H-indolo[2,3-b]quinolines is described using indole C3 alkylation and a one-pot reduction-cyclization-aromatization sequence. The synthesis of the parent 6H-indolo[2,3-b] quinoline system constitutes a formal synthesis of the alkaloid neocryptolepine (cryptotackieine).
    DOI:
    10.1055/s-0031-1290812
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文献信息

  • Materials for organic electroluminescent devices
    申请人:Merck Patent GmbH
    公开号:US10923665B2
    公开(公告)日:2021-02-16
    The present invention relates to compounds suitable for use in electronic devices, and to electronic devices, especially organic electroluminescent devices, comprising these compounds.
    本发明涉及适用于电子设备的化合物,以及包括这些化合物的电子设备,特别是有机电致发光器件。
  • Synthesis and Antiplasmodial Activity of Aminoalkylamino-Substituted Neocryptolepine Derivatives
    作者:Ibrahim El Sayed、Pieter Van der Veken、Koen Steert、Liene Dhooghe、Steven Hostyn、Gitte Van Baelen、Guy Lemière、Bert U. W. Maes、Paul Cos、Louis Maes、Jurgen Joossens、Achiel Haemers、Luc Pieters、Koen Augustyns
    DOI:10.1021/jm801490z
    日期:2009.5.14
    A series of chloro- and aminoalkylamino-substituted neocryptolepine (5-methyl-5H-indolo[2,3-b]quinoline) derivatives were synthesized and evaluated as antiplasmodial agents. The evaluation also included cytotoxicity (MRCS cells), inhibition of beta-hematin formation, and DNA interactions (DNA-methyl green assay). Introduction of aminoalkylamino chains increased the antiplasmodial activity of the neocryptolepine core substantially. The most efficient compounds showed antiplasmodial activities in the nanomolar range. N-1,N-1-Diethyl-N-4-(5-methyl-5H-indolo[2,3-b]quinolin-8-yl)pentane-1,4-diamine 11c showed an IC50 of 0.01 mu M and a selectivity index of 1800.
  • Cu(OTf)<sub>2</sub> Enhanced Intramolecular Nucleophilic <i>N</i>-Arylation of 2-Amino-3-arylquinolines
    作者:Anwesha Bhattacharya、Nayanthara Ramesh Babu、Debashruti Bandyopadhyay、Saravanan Peruncheralathan
    DOI:10.1021/acs.joc.3c00645
    日期:2023.7.7
  • MATERIALIEN FÜR ORGANISCHE ELEKTROLUMINESZENZVORRICHTUNGEN
    申请人:Merck Patent GmbH
    公开号:EP3583104B1
    公开(公告)日:2021-06-09
  • MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES
    申请人:Merck Patent GmbH
    公开号:US20200044162A1
    公开(公告)日:2020-02-06
    The present invention relates to compounds suitable for use in electronic devices, and to electronic devices, especially organic electroluminescent devices, comprising these compounds.
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