2-benzyl-4-methyl-2,8-diazaspiro[4.5]decan-1-one | 1429173-12-5

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 氮杂螺癸烷衍生物
• 英文名称: 2-benzyl-4-methyl-2,8-diazaspiro[4.5]decan-1-one
• 英文别名: 2-Benzyl-4-methyl-2,8-diazaspiro[4.5]decan-1-one
• CAS: 1429173-12-5
• 化学式: C₁₆H₂₂N₂O
• 分子量: 258.363
• InChiKey: PNZTWDBIKSCOCQ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.56
• 拓扑面积：
  32.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-benzyl-4-methyl-2,8-diazaspiro[4.5]decan-1-one 在 盐酸 作用下， 以 乙醚 为溶剂， 反应 0.08h， 以19 mg的产率得到2-benzyl-4-methyl-2,8-diazaspiro[4.5]decan-1-one hydrochloride
  参考文献：
  名称：

  Spirocyclic Dihydropyridines by Electrophile-Induced Dearomatizing Cyclization of N-Alkenyl Pyridinecarboxamides

  摘要：

  On treatment with acylating or sulfonylating agents, N-alkenyl pyridine carboxamides (N-pyridinecarbonyl enamines) undergo a dearomatizing cyclization initiated by pyridine acylation and followed by intramolecular trapping of the resulting pyridinium cation. The products are spirocyclic dihydropyridines which may be further elaborated to spirocyclic heterocycles with drug-like features.

  DOI：

  10.1021/ol400571j
• 作为产物：
  描述：

  异烟酸酰氯 在 2,6-二甲基吡啶 、 palladium 10% on activated carbon 、 氢气 、 三乙胺 、 potassium hydroxide 作用下， 以 乙醇 、 二氯甲烷 、 乙酸乙酯 为溶剂， 150.0 ℃ 、9.0 MPa 条件下， 反应 24.03h， 生成 2-benzyl-4-methyl-2,8-diazaspiro[4.5]decan-1-one
  参考文献：
  名称：

  Spirocyclic Dihydropyridines by Electrophile-Induced Dearomatizing Cyclization of N-Alkenyl Pyridinecarboxamides

  摘要：

  On treatment with acylating or sulfonylating agents, N-alkenyl pyridine carboxamides (N-pyridinecarbonyl enamines) undergo a dearomatizing cyclization initiated by pyridine acylation and followed by intramolecular trapping of the resulting pyridinium cation. The products are spirocyclic dihydropyridines which may be further elaborated to spirocyclic heterocycles with drug-like features.

  DOI：

  10.1021/ol400571j

文献信息

• Spirocyclic Dihydropyridines by Electrophile-Induced Dearomatizing Cyclization of N-Alkenyl Pyridinecarboxamides
  作者：Jemma Senczyszyn、Heloise Brice、Jonathan Clayden

  DOI：10.1021/ol400571j

  日期：2013.4.19

  On treatment with acylating or sulfonylating agents, N-alkenyl pyridine carboxamides (N-pyridinecarbonyl enamines) undergo a dearomatizing cyclization initiated by pyridine acylation and followed by intramolecular trapping of the resulting pyridinium cation. The products are spirocyclic dihydropyridines which may be further elaborated to spirocyclic heterocycles with drug-like features.