2-(naphthalen-1-yl)-3-nitropyridine | 1310472-36-6

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 2-(naphthalen-1-yl)-3-nitropyridine
• 英文别名: 2-Naphthalen-1-yl-3-nitropyridine
• CAS: 1310472-36-6
• 化学式: C₁₅H₁₀N₂O₂
• 分子量: 250.257
• InChiKey: SENFTMFTRTYXLP-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  19
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  58.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-(naphthalen-1-yl)-3-nitropyridine 在 1,2-双(二苯基膦)乙烷 作用下， 反应 5.0h， 以89%的产率得到7H-benzo[e]pyrido[3,2-b]indole
  参考文献：
  名称：

  Solvent-free synthesis of δ-carbolines/carbazoles from 3-nitro-2-phenylpyridines/2-nitrobiphenyl derivatives using DPPE as a reducing agent

  摘要：

  A green and efficient preparation of functionalized delta-carbolines/carbazoles via reductive ring closure by 1,2-bis(dipenylphosphino)ethane under solvent-free conditions is described. The starting materials 3-nitro-2-phenylpyridines/2-nitrobiphenyl derivatives are readily prepared through Suzuki-Miyaura cross-coupling reaction from commercially available compounds. And the polar by-product ethane-1,2-diylbis(diphenylphosphine oxide) is easily removed from the relatively polar reaction mixture. Various substituted delta-carbolines/carbazoles are obtained in acceptable yields. It is particularly worth mentioning that substrates with electron-withdrawing groups (EWG) also give the desired products in good yield. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.06.027
• 作为产物：
  描述：

  1-溴代萘 、 (3-nitropyridin-2-yl)boronic acid 在 四(三苯基膦)钯 、 potassium carbonate 作用下， 以 乙醇 、 水 、 甲苯 为溶剂， 反应 3.0h， 以61%的产率得到2-(naphthalen-1-yl)-3-nitropyridine
  参考文献：
  名称：

  헤테로고리 화합물 및 이를 이용한 유기발광소자

  摘要：

  本规范针对新型杂环化合物及其在有机发光器件中的应用。

  公开号：

  KR20160007438A

文献信息

• [EN] PYRROLO[2,3-C]PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF<br/>[FR] DERIVES DE PYRROLO[2,3-C]PYRIDINE ET LEURS PROCEDES DE PREPARATION
  申请人：YUHAN CORP

  公开号：WO2006025716A1

  公开（公告）日：2006-03-09

  The present invention provides novel pyrrolo[2,3-c]pyridine derivatives or pharmaceutically acceptable salts thereof, processes for the preparation thereof, and compositions comprising the same. The pyrrolo[2,3-c]pyridine derivatives or pharmaceutically acceptable salts thereof of the present invention have excellent proton pump inhibition effects and possess the ability to attain a reversible proton pump inhibitory effect.

  本发明提供了新型吡咯并[2,3-c]吡啶衍生物或其药用可接受的盐，其制备方法，以及包含相同的组合物。本发明的吡咯并[2,3-c]吡啶衍生物或其药用可接受的盐具有出色的质子泵抑制效果，并具有达到可逆质子泵抑制效果的能力。
• 一种有机半导体化合物和使用该化合物的有 机电致发光器件
  申请人：江西冠能光电材料有限公司

  公开号：CN106977527B

  公开（公告）日：2019-11-08

  本发明公开了一种有机半导体化合物和使用该化合物的有机电致发光器件，涉及一种有机发光二极管，其由一个阴极，一个阳极以及阴极与阳极间的有机半导体层构成，所述的有机半导体发光层中含有一有机半导体化合物结构式为：其特征是所述的有机半导体由一含带吸电性氮原子的苯环和萘环的芳杂环组成，其中吡咯环氮原子上还联有拓展∏共轭的取代基、或是扩大分子量的连接基L1。使用所述的有机半导体作为发光层应用，可提高发光效率，延长器件工作寿命。
• PYRROLO[2,3-C]PYRIDINE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF
  申请人：Kim Jae-Gyu

  公开号：US20070219230A1

  公开（公告）日：2007-09-20

  The present invention provides novel pyrrolo[2,3-c]pyridine derivatives or pharmaceutically acceptable salts thereof, processes for the preparation thereof, and compositions comprising the same. The pyrrolo[2,3-c]pyridine derivatives or pharmaceutically acceptable salts thereof of the present invention have excellent proton pump inhibition effects and possess the ability to attain a reversible proton pump inhibitory effect.

  本发明提供了新型吡咯并[2,3-c]吡啶衍生物或其药学上可接受的盐，其制备方法以及包含它们的组合物。本发明的吡咯并[2,3-c]吡啶衍生物或其药学上可接受的盐具有优异的质子泵抑制作用，并具有可逆的质子泵抑制作用。
• Solvent-free synthesis of δ-carbolines/carbazoles from 3-nitro-2-phenylpyridines/2-nitrobiphenyl derivatives using DPPE as a reducing agent
  作者：Haixia Peng、Xuxing Chen、Yanhong Chen、Qian He、Yuyuan Xie、Chunhao Yang

  DOI：10.1016/j.tet.2011.06.027

  日期：2011.8

  A green and efficient preparation of functionalized delta-carbolines/carbazoles via reductive ring closure by 1,2-bis(dipenylphosphino)ethane under solvent-free conditions is described. The starting materials 3-nitro-2-phenylpyridines/2-nitrobiphenyl derivatives are readily prepared through Suzuki-Miyaura cross-coupling reaction from commercially available compounds. And the polar by-product ethane-1,2-diylbis(diphenylphosphine oxide) is easily removed from the relatively polar reaction mixture. Various substituted delta-carbolines/carbazoles are obtained in acceptable yields. It is particularly worth mentioning that substrates with electron-withdrawing groups (EWG) also give the desired products in good yield. (C) 2011 Elsevier Ltd. All rights reserved.
• EP1784404A4
  申请人：——

  公开号：EP1784404A4

  公开（公告）日：2009-09-09