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1-benzyl-2-(4-chlorophenyl)-4,5-diphenyl-1H-imidazole

中文名称
——
中文别名
——
英文名称
1-benzyl-2-(4-chlorophenyl)-4,5-diphenyl-1H-imidazole
英文别名
1-benzyl-2-(4-chlorophenyl)-4,5-diphenylimidazole
1-benzyl-2-(4-chlorophenyl)-4,5-diphenyl-1H-imidazole化学式
CAS
——
化学式
C28H21ClN2
mdl
——
分子量
420.941
InChiKey
YFKUAGWPSLDAMX-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):
    7.2
  • 重原子数:
    31
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.04
  • 拓扑面积:
    17.8
  • 氢给体数:
    0
  • 氢受体数:
    1

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:
    氯化苄2-(4-氯苯基)-4,5-二苯基咪唑 在 sodium hydride 作用下, 以 四氢呋喃 为溶剂, 以49%的产率得到1-benzyl-2-(4-chlorophenyl)-4,5-diphenyl-1H-imidazole
    参考文献:
    名称:
    Synthesis and analgesic activity of some 1-benzyl-2-substituted-4,5-diphenyl-1H-imidazole derivatives
    摘要:
    In this study, derivatives of 1-benzyl-2-substituted-4,5-diphenyl-1H-imidazole were synthesized and their analgesic activity assayed in two tests. 1,2,4,5-Tetrasubstituted imidazole compounds were obtained by the treatment of purified imidazole compounds with benzyl chloride in the presence of sodium hydride. The structure elucidation of the compounds was performed by IR, H-1-NMR and mass spectroscopic data and elemental analysis results. Generally the prepared compound exhibited only moderate analgesic activity in mice at the dose of 100 mg/kg i.p.; however, a few of them exhibited good activity, almost equivalent to that of morphine at 1 mg/kg i.p. was observed. At the above dosage, no toxicity was observed for all compounds. (C) 2001 Elsevier Science S.A. All rights reserved.
    DOI:
    10.1016/s0014-827x(01)01076-x
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文献信息

  • Visible light-emitting diode light-driven one-pot four component synthesis of poly-functionalized imidazoles under catalyst- and solvent-free conditions
    作者:Geetika Patel、Ashok Raj Patel、Subhash Banerjee
    DOI:10.1039/d0nj02527e
    日期:——

    A visible light-emitting diode light-driven green and sustainable protocol has been demonstrated for the one-pot four component synthesis of poly-functionalized imidazoles under catalyst- and solvent-free conditions.

    已经展示了一种可见光发光二极管驱动的绿色可持续协议,用于在无催化剂和无溶剂条件下进行一锅式四组分合成多官能基咪唑。
  • An Effective and New Method for the Synthesis of Polysubstituted Imidazoles by the Use of CrCl<sub>3</sub>.6H<sub>2</sub>O as a Green and Reusable Catalyst: Synthasis of Some Novel Imidazole Derivatives
    作者:Bahador Karami、Khalil Eskandari、Mahnaz Farahi、Akram Barmas
    DOI:10.1002/jccs.201100555
    日期:2012.4
    environmentally adapted synthesis of polysubstituted imidazoles in one‐pot is found. The multicomponent reaction of various aldehydes, benzil, aliphatic and aromatic primary amines and ammonium acetate under solvent‐free condition is explained. The highly efficient role of CrCl3.6H2O as catalyst in this synthesis was shown. By this advantage, several polysubstituted imidazoles as pharmaceutical important
    发现了一种新的,高效且环保的单锅合成多取代咪唑的方法。解释了在无溶剂条件下各种醛,苄基,脂肪族和芳香族伯胺与乙酸铵的多组分反应。显示了CrCl 3 .6H 2 O在该合成中作为催化剂的高效作用。利用这一优点,可以高产率和高纯度制备几种作为药物重要分子的多取代的咪唑。该方法是合成咪唑衍生物的非常容易且快速的反应。粗产物重结晶,得到结晶纯产物。此外,催化剂表现出显着的可重复使用活性。
  • One-Pot Synthesis of Polysubstituted Imidazoles Based on Pd(OAc)2/Ce(SO4)2/Bi(NO3)3 Trimetallic Cascade of Decarboxylation/Wacker-Type Oxidation/Debus–Radziszewski Reaction
    作者:Wei Sun、Mingjuan Zhang、Peilang Li、Yiqun Li
    DOI:10.1055/s-0037-1611835
    日期:2019.9
    Abstract A novel and highly efficient one-pot synthesis of polysubstituted imidazoles from α-hydroxyphenylacetic acids, diphenylacetylene, and amines has been achieved by Pd(OAc)2/Ce(SO4)2/Bi(NO3)3 trimetallic catalytic system. A series of control experiments showed that this overall reaction occurs through a one-pot cascade process combining the steps of decarboxylation of α-hydroxyphenylacetic acids
    抽象的 通过Pd(OAc)2 / Ce(SO 4)2 / Bi(NO 3)3从α-羟基苯基乙酸,二苯乙炔和胺中合成新颖高效的一锅合成咪唑三金属催化体系。一系列对照实验表明,整个反应是通过一锅级联过程完成的,该过程结合了α-羟基苯基乙酸的脱羧步骤,二苯基乙炔的Wacker型氧化步骤以及原位生成的芳基醛和苯的Debus-Radziszewski环合反应,以及胺。该反应代表使用α-羟基苯基乙酸和二苯乙炔作为芳基醛和β-二酮的来源的新颖的多组分反应。该方法具有宽泛的底物范围和良好的官能团耐受性,可在温和条件下以优异的收率(72–88%)组装相应的多取代的咪唑。 通过Pd(OAc)2 / Ce(SO 4)2 / Bi(NO 3)3从α-羟基苯基乙酸,二苯乙炔和胺中合成新颖高效的一锅合成咪唑三金属催化体系。一系列对照实验表明,整个反应是通过一锅级联过程完成的,该过程结合了α-羟基苯基乙酸的脱羧步骤,二
  • An efficient and one-pot synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles catalyzed by InCl3·3H2O
    作者:Saikat Das Sharma、Parasa Hazarika、Dilip Konwar
    DOI:10.1016/j.tetlet.2008.02.053
    日期:2008.3
    InCl3·3H2O was found to be a mild and effective catalyst for the efficient, one-pot, three component synthesis of 2,4,5-trisubstituted imidazoles at room temperature. Moreover, the utility of this protocol was further explored conveniently for the one-pot, four component synthesis of 1,2,4,5-tetrasubstituted imidazoles in high yields.
    发现InCl 3 ·3H 2 O是在室温下高效,一锅,三组分合成2,4,5-三取代的咪唑的温和有效的催化剂。此外,可以方便地进一步探索该方案的实用性,以高产率一锅,四组分合成1,2,4,5-四取代的咪唑。
  • Facile and rapid synthesis of some novel polysubstituted imidazoles by employing magnetic Fe_3O_4 nanoparticles as a high efficient catalyst
    作者:BAHADOR KARAMI、KHALIL ESKANDARI、ABDOLMOHAMMAD GHASEMI
    DOI:10.3906/kim-1112-49
    日期:——
    Multicomponent, one-pot, highly efficient, and environmentally adapted synthesis of some novel polysubstituted imidazoles by the use of various aldehydes, benzil, aliphatic, and aromatic primary amines and ammonium acetate in the presence of Fe_3O_4 nanoparticles as catalyst under solvent-free condition is explained. A highly efficient role of Fe_3O_4 nanoparticles as catalyst in this synthesis was shown. By this advantage, several polysubstituted imidazoles as pharmaceutical important molecules can be prepared in high yield and high purity. This method is very easy and rapid for the synthesis of imidazole derivatives. All products were deduced from their IR and NMR spectroscopic data. The Fe_3O_4 nanoparticles were characterized by powdered X-ray diffraction (XRD), transmission electron microscopy (TEM), and FT-IR spectroscopy.
    本文阐述了在无溶剂条件下,利用多种醛、苯偶酰、脂肪族和芳香族一级胺以及乙酸铵作为原料,通过Fe_3O_4纳米颗粒作为催化剂,实现多组分、一锅法、高效且环境适应性的新型多取代咪唑合成方法。研究表明,Fe_3O_4纳米颗粒在这一合成过程中表现出高效的催化作用。利用这一优势,可以高产率和高纯度地制备出若干具有重要药学意义的多取代咪唑分子。该方法操作简便、反应迅速,适用于咪唑衍生物的合成。所有产物均通过其红外光谱和核磁共振光谱数据得以推导。Fe_3O_4纳米颗粒则通过粉末X射线衍射(XRD)、透射电子显微镜(TEM)以及傅里叶变换红外光谱(FT-IR)进行表征。
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