N-[(E)-1-(4-methylphenyl)methylidene]-N-(5-quinolyl)amine

• 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-[(E)-1-(4-methylphenyl)methylidene]-N-(5-quinolyl)amine
• 英文别名: 1-(4-methylphenyl)-N-quinolin-5-ylmethanimine
• 化学式: C₁₇H₁₄N₂
• 分子量: 246.312
• InChiKey: IHVZIVGPCGMAJV-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  25.2
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  N-[(E)-1-(4-methylphenyl)methylidene]-N-(5-quinolyl)amine 以 正丁醇 为溶剂， 生成
  参考文献：
  名称：

  Synthesis of methyl 7-aryl(hetaryl, cyclohexenyl)-10-(1,3-benzodioxol-5-yl)-8-oxo-7,8,9,10,11,12-hexahydro-benzo[b][1,7]phenanthroline-9-carboxylates

  摘要：

  Three-component condensation of quinolin-5-amine with methyl 2-(1,3-benzodioxol-5-yl)-4,6-dioxocyclohexane-1-carboxylates and aromatic aldehydes (or cyclohex-3-ene-1-carbaldehyde) afforded new hexahydrobenzo[b][1,7]phenanthroline derivatives. The condensation in butan-1-ol is strictly regioselective but not stereoselective, so that mixtures of cis- and trans-isomeric methyl 7-aryl(hetaryl, cyclohexenyl)-10-(1,3-benzodioxol-5-yl)-8-oxo-7,8,9,10,11,12-hexahydrobenzo[b][1,7]phenanthroline-9-carboxylates at a ratio of similar to 40: 60% are formed.

  DOI：

  10.1134/s1070428013090157
• 作为产物：
  描述：

  5-氨基喹啉 、 对甲基苯甲醛 以 正丁醇 为溶剂， 生成 N-[(E)-1-(4-methylphenyl)methylidene]-N-(5-quinolyl)amine
  参考文献：
  名称：

  Synthesis of methyl 7-aryl(hetaryl, cyclohexenyl)-10-(1,3-benzodioxol-5-yl)-8-oxo-7,8,9,10,11,12-hexahydro-benzo[b][1,7]phenanthroline-9-carboxylates

  摘要：

  Three-component condensation of quinolin-5-amine with methyl 2-(1,3-benzodioxol-5-yl)-4,6-dioxocyclohexane-1-carboxylates and aromatic aldehydes (or cyclohex-3-ene-1-carbaldehyde) afforded new hexahydrobenzo[b][1,7]phenanthroline derivatives. The condensation in butan-1-ol is strictly regioselective but not stereoselective, so that mixtures of cis- and trans-isomeric methyl 7-aryl(hetaryl, cyclohexenyl)-10-(1,3-benzodioxol-5-yl)-8-oxo-7,8,9,10,11,12-hexahydrobenzo[b][1,7]phenanthroline-9-carboxylates at a ratio of similar to 40: 60% are formed.

  DOI：

  10.1134/s1070428013090157

文献信息

• Barbituric acid in the synthesis of fused 1,7-phenanthroline derivatives
  作者：N. G. Kozlov、A. B. Tereshko

  DOI：10.1134/s1070428014070124

  日期：2014.7
• Synthesis of methyl 7-aryl(hetaryl, cyclohexenyl)-10-(1,3-benzodioxol-5-yl)-8-oxo-7,8,9,10,11,12-hexahydro-benzo[b][1,7]phenanthroline-9-carboxylates
  作者：N. G. Kozlov、A. B. Tereshko

  DOI：10.1134/s1070428013090157

  日期：2013.9

  Three-component condensation of quinolin-5-amine with methyl 2-(1,3-benzodioxol-5-yl)-4,6-dioxocyclohexane-1-carboxylates and aromatic aldehydes (or cyclohex-3-ene-1-carbaldehyde) afforded new hexahydrobenzo[b][1,7]phenanthroline derivatives. The condensation in butan-1-ol is strictly regioselective but not stereoselective, so that mixtures of cis- and trans-isomeric methyl 7-aryl(hetaryl, cyclohexenyl)-10-(1,3-benzodioxol-5-yl)-8-oxo-7,8,9,10,11,12-hexahydrobenzo[b][1,7]phenanthroline-9-carboxylates at a ratio of similar to 40: 60% are formed.