3,3-bis(azidomethyl)-1,5-dioxaspiro[5.5]undecane | 121705-23-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 3,3-bis(azidomethyl)-1,5-dioxaspiro[5.5]undecane
• CAS: 121705-23-5
• 化学式: C₁₁H₁₈N₆O₂
• 分子量: 266.303
• InChiKey: BJLQDUBQYUOEBU-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  19.0
• 可旋转键数：
  4.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  115.98
• 氢给体数：
  0.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  3,3-bis(azidomethyl)-1,5-dioxaspiro[5.5]undecane 在 Lindlar's catalyst 氢气 作用下， 以 乙醇 为溶剂， 生成 [3-(Aminomethyl)-1,5-dioxaspiro[5.5]undecan-3-yl]methanamine
  参考文献：
  名称：

  A new family of water-soluble, third-generation antitumor platinum complexes

  摘要：

  [1,1-Cyclobutanedicarboxylato(2)-O,O'](1,3-dioxane-5,5-dimethan amine- N,N')platinum(II), 3a, a third generation, very water-soluble platinum complex, has been synthesized along with several of its analogues. All members of the new family contain a 1,3-dioxane or 1,3-dioxolane-1,3-diamine as their basic ligand, a moiety which contributes to their increased water solubility, and a bidentate acid ligand, which is responsible for their good stability. They were all easily crystallized and characterized by 1H NMR and elemental analysis, and the parent complex 3a was further characterized by 13C NMR. Their very desirable physical properties combined with their broad spectrum of antitumor activity and reduced toxicity make them good candidates of further development.

  DOI：

  10.1021/jm00129a008
• 作为产物：
  描述：

  3,3-bis(bromomethyl)-1,5-dioxaspiro<5.5>undecane 在 sodium azide 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 3,3-bis(azidomethyl)-1,5-dioxaspiro[5.5]undecane
  参考文献：
  名称：

  A new family of water-soluble, third-generation antitumor platinum complexes

  摘要：

  [1,1-Cyclobutanedicarboxylato(2)-O,O'](1,3-dioxane-5,5-dimethan amine- N,N')platinum(II), 3a, a third generation, very water-soluble platinum complex, has been synthesized along with several of its analogues. All members of the new family contain a 1,3-dioxane or 1,3-dioxolane-1,3-diamine as their basic ligand, a moiety which contributes to their increased water solubility, and a bidentate acid ligand, which is responsible for their good stability. They were all easily crystallized and characterized by 1H NMR and elemental analysis, and the parent complex 3a was further characterized by 13C NMR. Their very desirable physical properties combined with their broad spectrum of antitumor activity and reduced toxicity make them good candidates of further development.

  DOI：

  10.1021/jm00129a008