methyl 7-methyl-2-(4-nitrophenyl)-6-(trifluoromethyl)-5,6,7,8-tetrahydro-1,7-naphthyridine-6-carboxylate | 1400553-78-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氮杂萘
• 英文名称: methyl 7-methyl-2-(4-nitrophenyl)-6-(trifluoromethyl)-5,6,7,8-tetrahydro-1,7-naphthyridine-6-carboxylate
• 英文别名: Methyl 7-methyl-2-(4-nitrophenyl)-6-(trifluoromethyl)-5,8-dihydro-1,7-naphthyridine-6-carboxylate；methyl 7-methyl-2-(4-nitrophenyl)-6-(trifluoromethyl)-5,8-dihydro-1,7-naphthyridine-6-carboxylate
• CAS: 1400553-78-7
• 化学式: C₁₈H₁₆F₃N₃O₄
• 分子量: 395.338
• InChiKey: RQVGYNGWJCEMMF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.1
• 重原子数：
  28
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  88.2
• 氢给体数：
  0
• 氢受体数：
  9

反应信息

• 作为产物：
  描述：

  methyl 3-methyl-8-(4-nitrobenzoyl)-4-(trifluoromethyl)-3-azabicyclo[4.2.0]octa-1(8),5-diene-4-carboxylate 在 四氢吡咯 、 ammonium acetate 作用下， 以 1,4-二氧六环 、 溶剂黄146 为溶剂， 反应 1.33h， 生成 methyl 7-methyl-2-(4-nitrophenyl)-6-(trifluoromethyl)-5,6,7,8-tetrahydro-1,7-naphthyridine-6-carboxylate
  参考文献：
  名称：

  Cyclobutene Ring-Opening of Bicyclo[4.2.0]octa-1,6-dienes: Access to CF₃-Substituted 5,6,7,8-Tetrahydro-1,7-naphthyridines

  摘要：

  An efficient method for the synthesis of novel CF3-substituted tetrahydro-1,7-naphthyridines including cyclic alpha-amino acid derivatives has been developed. The method is based on unusual cyclobutene ring-opening of bicyclo[4.2.0]octa-1,6-dienes with pyrrolidine to afford the corresponding 1,5-diketones followed by their heterocyclization. A convenient one-pot procedure has been also elaborated starting from readily available trifluoromethylated 1,6-allenynes.

  DOI：

  10.1021/jo301501r

文献信息

• Cyclobutene Ring-Opening of Bicyclo[4.2.0]octa-1,6-dienes: Access to CF₃-Substituted 5,6,7,8-Tetrahydro-1,7-naphthyridines
  作者：Artur K. Mailyan、Alexander S. Peregudov、Pierre H. Dixneuf、Christian Bruneau、Sergey N. Osipov

  DOI：10.1021/jo301501r

  日期：2012.10.5

  An efficient method for the synthesis of novel CF3-substituted tetrahydro-1,7-naphthyridines including cyclic alpha-amino acid derivatives has been developed. The method is based on unusual cyclobutene ring-opening of bicyclo[4.2.0]octa-1,6-dienes with pyrrolidine to afford the corresponding 1,5-diketones followed by their heterocyclization. A convenient one-pot procedure has been also elaborated starting from readily available trifluoromethylated 1,6-allenynes.