N,N-dimethyl-4-(quinolin-4-yl)aniline | 22192-00-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: N,N-dimethyl-4-(quinolin-4-yl)aniline
• 英文别名: 4-(4-dimethylaminophenyl)quinoline；N,N-dimethyl-4-quinolin-4-yl-aniline；4-(p-Dimethylaminophenyl)-chinolin；N,N-dimethyl-4-quinolin-4-ylaniline
• CAS: 22192-00-3
• 化学式: C₁₇H₁₆N₂
• 分子量: 248.327
• InChiKey: RJVANNWGUVBGDN-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  16.1
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  3-(4-dimethylamino-phenyl)-propenal 在 三氟化硼乙醚 、 亚硝酸异戊酯 、 三氯乙酸 作用下， 以 四氢呋喃 、 苯 为溶剂， 反应 1.0h， 生成 N,N-dimethyl-4-(quinolin-4-yl)aniline
  参考文献：
  名称：

  Synthesis of Quinolines from N-Tosyl-1-azadienes

  摘要：

  A route to aryl-substituted quinolines from N-tosyl 1-azadienes is described. The key steps are a [4+2] cycloaddition with benzyne followed by base treatment of the 1,4-dihydroquinoline product. The N-tosyl 1-azadienes were prepared from readily accessible cinnamaldehyde and chalcone substrates by condensation with p-TsNH2. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.

  DOI：

  10.1080/00397911.2012.726388

文献信息

• Substituted Acetylene Derivatives and their Use as Positive Allosteric Modulators of mGluR4
  申请人：MERCK PATENT GMBH

  公开号：US20150376182A1

  公开（公告）日：2015-12-31

  The present invention relates to novel acetylene derivatives as positive allosteric modulators for modulating metabotropic glutamate receptor subtype 4 (mGluR4) and/or altering glutamate level or glutamatergic signalling.

  本发明涉及新型乙炔衍生物，作为正向变构调节剂，用于调节代谢型谷氨酸受体亚型4（mGluR4）和/或改变谷氨酸水平或谷氨酸信号传导。
• Synthesis of Quinolines from <i>N</i>-Tosyl-1-azadienes
  作者：Sean Stokes、Keith T. Mead

  DOI：10.1080/00397911.2012.726388

  日期：2013.10.2

  A route to aryl-substituted quinolines from N-tosyl 1-azadienes is described. The key steps are a [4+2] cycloaddition with benzyne followed by base treatment of the 1,4-dihydroquinoline product. The N-tosyl 1-azadienes were prepared from readily accessible cinnamaldehyde and chalcone substrates by condensation with p-TsNH2. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) to view the free supplemental file.