4-(3,4-dichlorophenyl)-2,6-diphenylpyridine

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡啶及其衍生物
• 英文名称: 4-(3,4-dichlorophenyl)-2,6-diphenylpyridine
• 英文别名: 4‑(3,4‑dichlorophenyl)‑2,6‑diphenylpyridine；4-(3,4-Dichlorophenyl)-2,6-diphenylpyridine
• 化学式: C₂₃H₁₅Cl₂N
• 分子量: 376.285
• InChiKey: KSJSPTLGFAPNEK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.5
• 重原子数：
  26
• 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：
  12.9
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  3-(3,4-dichlorophenyl)-1-phenyl-2-propen-1-one 在 aluminum oxide 、 bismuth(III) nitrate 尿素 作用下， 以70%的产率得到4-(3,4-dichlorophenyl)-2,6-diphenylpyridine
  参考文献：
  名称：

  一种新的方便的一锅法固体支持的2,4,6-三芳基吡啶的合成方法

  摘要：

  描述了一种新的，方便，有效且具有成本效益的一锅固支持的硝酸Bi（III）-Al 2 O 3，由亚苄基苯乙酮和尿素，硫脲或其衍生物合成2,4,6-三芳基吡啶。该反应似乎是通过对Bi（III）烯丙基化的亚苄基苯乙酮进行β加氧，然后进行迈克尔加成，同时同时逆向羟醛歧化和随后的催化氧化和脱水而进行的。

  DOI：

  10.1016/j.tetlet.2005.11.043

文献信息

• Merrifield resin-supported quinone as an efficient biomimetic catalyst for metal-free, base-free, chemoselective synthesis of 2,4,6-trisubstituted pyridines
  作者：Qing Yang、Yilin Zhang、Wei Zeng、Zheng-Chao Duan、Xinxin Sang、Dawei Wang

  DOI：10.1039/c9gc02409c

  日期：——

  (EDX). This supported quinone catalyst exhibited excellent catalytic reactivity for chemoselective synthesis of 2,4,6-trisubstituted pyridines, providing an efficient and green method for the synthesis of pyridine derivatives under mild conditions. Mechanistic investigations were conducted to gain insights into the heterogeneous biomimetic catalyst as well as the resulting transformation. The successful

  首次在温和条件下开发了2,4,6-三取代吡啶的无金属，无碱，仿生和化学选择性合成方法。均质仿生催化剂-可回收的Merrifield树脂负载的醌-通过傅里叶变换红外光谱（FT-IR），X射线光电子能谱（XPS）和能量色散X射线能谱（EDX）进行了充分表征。这种负载的醌催化剂对化学选择性合成2,4,6-三取代的吡啶具有优异的催化反应活性，为在温和条件下合成吡啶衍生物提供了一种高效而绿色的方法。进行了机理研究，以深入了解异质仿生催化剂以及由此产生的转化。
• Design and application of (Fe3O4)-GOTfOH based AgNPs doped starch/PEG-poly (acrylic acid) nanocomposite as the magnetic nanocatalyst and the wound dress
  作者：Shayan Forouzandehdel、Maryam Meskini、Mina Rezghi Rami

  DOI：10.1016/j.molstruc.2020.128142

  日期：2020.8

  As a novel, recyclable nanocatalyst, (Fe3O4)-GO(TfOH) based Ag nanoparticles doped Starch/PEG-poly (acrylic acid) nanocomposite (Fe3O4@GO(TfOH)/Ag/St-PEG-AcA) was applied for one-pot synthesis of 2,4,6-triarylpyridine derivatives under water solvent conditions. The prepared nanocomposite was also evaluated in terms of biocompatibility for wound healing. Fe3O4@GO(TfOH)/Ag/St-PEG-AcA could be easily removed from the mixture of the reaction by an external magnet and recycled without a considerable decrease of activity even after 10 runs. The new nanocatalyst offered better efficiencies than other commercially available sulfonic acid catalysts. In terms of the bioactivity of nanocatalyst, good antimicrobial efficiency was confirmed on E. coli bacteria. Besides, histology of repaired wounds in Fe3O4@GO(TfOH)/Ag/St-PEG-AcA for a healed group of mice showed better fibroblast distribution and more compact collagen fiber organization compared to wounds in the control group. (C) 2020 Elsevier B.V. All rights reserved.
• A new and convenient one-pot solid supported synthesis of 2,4,6-triarylpyridines
  作者：Anil Kumar、Summon Koul、Tej K. Razdan、Kamal K. Kapoor

  DOI：10.1016/j.tetlet.2005.11.043

  日期：2006.1

  A new, convenient, efficient and cost-effective one-pot solid supported synthesis of 2,4,6-triarylpyridines from benzylideneacetophenones and urea, thiourea or their derivatives, using Bi(III) nitrate–Al2O3 is described. The reaction seems to proceed via β-oxygenation of Bi(III)-enolized benzylideneacetophenone followed by Michael addition, heteroannulation with simultaneous retro aldol disproportionation

  描述了一种新的，方便，有效且具有成本效益的一锅固支持的硝酸Bi（III）-Al 2 O 3，由亚苄基苯乙酮和尿素，硫脲或其衍生物合成2,4,6-三芳基吡啶。该反应似乎是通过对Bi（III）烯丙基化的亚苄基苯乙酮进行β加氧，然后进行迈克尔加成，同时同时逆向羟醛歧化和随后的催化氧化和脱水而进行的。