5-溴-1-甲基-3-苯基苯并咪唑-2-酮 | 79759-43-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并咪唑类
• 中文名称: 5-溴-1-甲基-3-苯基苯并咪唑-2-酮
• 英文名称: 5-bromo-1-methyl-3-phenyl-1,3-dihydro-benzoimidazol-2-one
• 英文别名: 5-bromo-1-methyl-3-phenyl-1H-benzo[d]imidazol-2(3H)-one；1,3-Dihydro-5-bromo-1-methyl-3-phenyl-2H-benzimidazol-2-one；5-bromo-1-methyl-3-phenylbenzimidazol-2-one
• CAS: 79759-43-6
• 化学式: C₁₄H₁₁BrN₂O
• 分子量: 303.158
• InChiKey: HRKLHPWXQWEIQA-UHFFFAOYSA-N

物化性质

• 熔点：
  176-178 °C
• 沸点：
  419.7±47.0 °C(Predicted)
• 密度：
  1.534±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  18
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.07
• 拓扑面积：
  23.6
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  5-bromo-N1-phenylbenzene-1,2-diamine 在 sodium ethanolate 、 potassium carbonate 作用下， 以 甲醇 、 乙醇 、 氯仿 为溶剂， 反应 23.0h， 生成 5-溴-1-甲基-3-苯基苯并咪唑-2-酮
  参考文献：
  名称：

  Bianchi; Butti; Rossi, European Journal of Medicinal Chemistry, 1981, vol. 16, # 4, p. 321 - 326

  摘要：

  DOI：

文献信息

• Metal-Free Oxidative C-H Amidation of<i>N</i>,<i>N′</i>-Diarylureas with PhI(OAc)₂: Synthesis of Benzimidazol-2-one Derivatives
  作者：Jipan Yu、Chang Gao、Zhixuan Song、Haijun Yang、Hua Fu

  DOI：10.1002/ejoc.201500726

  日期：2015.9

  compounds or intramolecular N-arylations using substrates with carbon-halogen bonds. However, the starting materials of these protocols are often not readily available. Herein, a simple and practical metal-free oxidative C–H amidation of N,N′-diarylureas has been developed that takes place at room temperature. This protocol uses readily available N,N′-diarylureas as the starting materials and inexpensive

  苯并咪唑-2-酮具有多种生物学功能，通常通过取代苯-1,2-二胺与含羰基化合物的反应或分子内N-芳基化反应制备，使用具有碳-卤键的底物。然而，这些协议的起始材料通常不容易获得。在此，开发了一种在室温下进行的简单实用的 N,N'-二芳基脲的无金属氧化 C-H 酰胺化反应。该协议使用现成的 N,N'-二芳基脲作为起始材料，使用廉价的 PhI(OAc)2 作为氧化剂，无需催化剂、配体或排除空气。本方法具有广泛的官能团耐受性，为合成 N-杂环提供了一种新的实用策略。
• Potassium Hydroxide/Dimethyl Sulfoxide Promoted Intramolecular Cyclization for the Synthesis of Benzimidazol-2-ones
  作者：Astrid Beyer、Christine M. M. Reucher、Carsten Bolm

  DOI：10.1021/ol2008878

  日期：2011.6.3

  A new protocol for intramolecular N-arylations of ureas to form benzimidazol-2-ones has been developed. The cyclization reaction occurs In the presence of KOH and DMSO at close to ambient temperature. Under these conditions the yields are high and a wide range of functional groups are tolerated.
• BIANCHI, M.;BUTTI, A.;ROSSI, S.;BARZAGHI, F.;MARCARIA, V., EUR. J. MED. CHEM.-CHIM. THER., 1981, 16, N 4, 321-326
  作者：BIANCHI, M.、BUTTI, A.、ROSSI, S.、BARZAGHI, F.、MARCARIA, V.

  DOI：——

  日期：——
• NITROGENATED HETEROCYCLIC DERIVATIVE, ELECTRON-TRANSPORTING MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENTS, AND ORGANIC ELECTROLUMINESCENT ELEMENT USING SAME
  申请人：Mizutani Sayaka

  公开号：US20130306955A1

  公开（公告）日：2013-11-21

  A specific nitrogen-containing heterocyclic compound having a urea structure, an electron transporting material containing the nitrogen-containing heterocyclic compound, and an organic electroluminescence device including a light emitting layer and an electron transporting layer between a cathode and an anode in which the electron transporting layer includes the electron transporting material or the nitrogen-containing heterocyclic derivative. An organic EL device exhibiting high emission efficiency even at low voltage and a material for organic EL devices are described.
• ORGANIC LIGHT-EMITTING DEVICE
  申请人：Samsung Display Co., Ltd.

  公开号：US20170047521A1

  公开（公告）日：2017-02-16

  An organic light-emitting device having high efficiency and improved lifespan is provided. The organic light-emitting device of the present disclosure includes: a first electrode; a second electrode facing the first electrode; an emission layer between the first electrode and the second electrode, the emission layer including a first compound; and an electron transport region between the emission layer and the second electrode, the electron transport region including an electron transport layer including a second compound and an electron control layer including a third compound, wherein the electron control layer is between the emission layer and the electron transport layer. The first compound may be represented by Formula 1, the second compound may be represented by Formula 2, and the third compound may be selected from compounds represented by Formula 1 and/or Formula 2: