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N-(4-fluorobenzylidene)[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-3-yl]amine | 1052605-31-8

中文名称
——
中文别名
——
英文名称
N-(4-fluorobenzylidene)[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-3-yl]amine
英文别名
N-(4-fluorobenzylidene)-2-(4-fluorophenyl)imidazo[1,2-a]pyridin-3-amine;1-(4-fluorophenyl)-N-[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-3-yl]methanimine
N-(4-fluorobenzylidene)[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-3-yl]amine化学式
CAS
1052605-31-8
化学式
C20H13F2N3
mdl
——
分子量
333.34
InChiKey
VWXKZKBAOKQPSL-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):
    5.3
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29.7
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    2-氨基吡啶对氟苯甲醛三甲基氰硅烷溴化二甲基溴化锍 作用下, 反应 11.0h, 以70%的产率得到N-(4-fluorobenzylidene)[2-(4-fluorophenyl)imidazo[1,2-a]pyridin-3-yl]amine
    参考文献:
    名称:
    (Bromodimethylsulfonium) bromide-catalyzed one-pot three-component synthesis of imidazo[1,2-a]pyridines
    摘要:
    Abstract(Bromodimethylsulfonium) bromide–catalyzed one‐pot multicomponent reaction of 2‐aminopyridine with aromatic aldehyde(s) and TMSCN yielding N‐benzylidene‐2‐phenylimidazo[1,2‐a]pyridines exclusively has been described. The reaction is solvent free, versatile, and takes significantly short time. J. Heterocyclic Chem., (2011).
    DOI:
    10.1002/jhet.518
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文献信息

  • BF<sub>3</sub>/MCM-41 as nano structured solid acid catalyst for the synthesis of 3-iminoaryl-imidazo[1,2-a]pyridines
    作者:Mohammad Abdollahi-Alibeik、Ali Rezaeipoor-Anari
    DOI:10.1039/c3cy00947e
    日期:——
    of aldehydes, 2-aminopyridines and trimethylsilyl cyanide was carried out in the presence of MCM-41 supported boron trifluoride (BF3/MCM-41) as a nanostructured solid acid catalyst for the synthesis of 3-iminoaryl-imidazo[1,2-a]pyridine derivatives. MCM-41 nanoparticles were synthesized by a sol–gel method and BF3/MCM-41 samples with various loading amounts of BF3 and different calcination temperatures
    在MCM-41负载的三氟化硼(BF 3 / MCM-41)作为用于合成3-亚基芳基的纳米结构固体酸催化剂的存在下,进行了各种类型的醛,2-氨基吡啶和三甲基甲硅烷化物的多组分反应。-咪唑并[1,2-a]吡啶衍生物。通过溶胶-凝胶法合成了MCM-41纳米粒子,并通过XRD,SEM和FT-IR技术制备了具有不同BF 3上样量和不同煅烧温度的BF 3 / MCM-41样品。催化性能实验表明,BF 3在400°C下煅烧的/ MCM-41具有最佳的催化活性。可回收性和可重复使用性实验表明,该催化剂可重复使用多次,且活性适度降低。
  • A one-pot four-component synthesis of N-arylidene-2-aryl-imidazo[1,2-a]azin-3-amines
    作者:Abbas Rahmati、Ali Moazzam、Zahra Khalesi
    DOI:10.1016/j.tetlet.2014.03.098
    日期:2014.7
    N-Arylidene-2-aryl-imidazo[1,2-a]azin-3-amines were synthesized via a one-pot, four-component condensation reaction using a 2-aminoazine, toluene-4-sulfonylmethyl isocyanide (TsCH2NC), and two equivalents of readily available aromatic aldehydes. The reaction was performed in diethyl ether as the solvent, with p-toluenesulfonic acid (p-TSA) as the catalyst at reflux temperature. (C) 2014 Elsevier Ltd. All rights reserved.
  • An efficient synthesis of 3-amino-2-arylimidazo[1,2-a]pyridines
    作者:Mehdi Adib、Esmail Sheibani、Long-Guan Zhu、Peiman Mirzaei
    DOI:10.1016/j.tetlet.2008.05.134
    日期:2008.8
    An efficient synthesis of 3-amino-2-arylimidazo[1,2-a]pyridines is described via a novel multicomponent reaction between 2-aminopyridines, benzaldehydes and imidazoline-2,4,5-trione under solvent-free conditions. (c) 2008 Elsevier Ltd. All rights reserved.
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