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1,1-bis[(8-quinolyl)oxy]methane | 120450-77-3

中文名称
——
中文别名
——
英文名称
1,1-bis[(8-quinolyl)oxy]methane
英文别名
bis(quinolyl-8-hydroxy)methane;8-(Quinolin-8-yloxymethoxy)quinoline
1,1-bis[(8-quinolyl)oxy]methane化学式
CAS
120450-77-3
化学式
C19H14N2O2
mdl
——
分子量
302.332
InChiKey
VICQLFXJBRZKNY-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):
    3.9
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    44.2
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    描述:
    8-羟基喹啉二氯甲烷四丁基溴化铵环己烯 作用下, 以72%的产率得到1,1-bis[(8-quinolyl)oxy]methane
    参考文献:
    名称:
    Petrosyan, V. A.; Niyazymbetov, M. E.; Baryshnikova, T. K., Doklady Chemistry, 1988, vol. 302, p. 283 - 285
    摘要:
    DOI:
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文献信息

  • Petrosyan, V. A.; Niyazymbetov, M. E.; Baryshnikova, T. K., Doklady Chemistry, 1988, vol. 302, p. 283 - 285
    作者:Petrosyan, V. A.、Niyazymbetov, M. E.、Baryshnikova, T. K.、Dorokhov, V. A.
    DOI:——
    日期:——
  • Phase transfer catalyzed synthesis of bis-quinolines: Antileishmanial activity in experimental visceral leishmaniasis and in vitro antibacterial evaluation
    作者:Partha Palit、Priyankar Paira、Abhijit Hazra、Sukdeb Banerjee、Asish Das Gupta、Sujata G. Dastidar、Nirup B. Mondal
    DOI:10.1016/j.ejmech.2008.04.014
    日期:2009.2
    A one-pot synthesis of some novel bis-quinolines has been achieved under phase transfer catalyzed conditions using 8-hydroxy quinoline derivatives as substrates. The synthesized analogues were evaluated for antileishmanial activity against Leishmania donovani promastigotes and amastigotes. The entire bis-quinolines showed efficacy in both in vitro and in vivo studies. Compound 5 (1,1-bis-[(5-chloro-8-quinolyl)oxy] methane) exhibited the most significant activity. Compounds 4 (1,1-bis-[(8-quinolyl)oxylmethane) and 9 (1,5-bis-[(2-methyl-8-quinolyl)oxy] pentane) also demonstrated significant leishmanicidal efficacy against established visceral leishmaniasis in BALB/c model. Ultrastructural studies of promastigotes treated with compound 5, demonstrated membrane blebbing, chromatin condensation and vacuolization in the parasites and the flagellated parasites became round shaped after treatment. Moreover, in vitro antibacterial activity of compound 5 against several bacterial strains revealed its promising efficacy. The findings suggested that 1,1-bis-[(5-chloro-8-quinolyl)oxy] methane (5) is a bright candidate to be considered as lead compound for leishmanicidal drug. (c) 2008 Elsevier Masson SAS. All rights reserved.
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