(1R,2R,6S,7R)-4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-azatricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione | 1028994-42-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 异吲哚及其衍生物
• 英文名称: (1R,2R,6S,7R)-4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-azatricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione
• 英文别名: (1S,2R,6S,7R)-4-(1,3-dioxoisoindol-2-yl)-4-azatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione
• CAS: 1028994-42-4
• 化学式: C₁₇H₁₂N₂O₄
• 分子量: 308.293
• InChiKey: GMSVGSJVKLMHMF-KGOITJQVSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  23
• 可旋转键数：
  0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.29
• 拓扑面积：
  74.8
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  (1R,2R,6S,7R)-4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-azatricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione 在 甲酸 、 双氧水 作用下， 以 水 为溶剂， 以83%的产率得到(1S,2R,6S,7S,8S,10R)-4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-9-oxa-4-azatetracyclo[5.3.1.0^2,6.0^8,10]undecane-3,5-dione
  参考文献：
  名称：

  Reactions of 4-amino-4-azatricyclo[5.2.1.02,6-endo ]dec-8-ene-3,5-dione with dicarboxylic acid anhydrides

  摘要：

  Reactions of 4-amino-4-azatricyclo[5.2.1.0(2,6-endo)]dec-8-ene-3,5-dione (hydrazinolysis product of endic anhydride) with succinic, maleic, cis-cyclohexane-1,2-dicarboxylic, endic, phthalic, and 1,8-naphthalic anhydrides were studied. Procedures for the preparation of the corresponding hydrazido acids and bis-imides were proposed. Their reactions with peroxyformic acid, depending on the substrate nature, led to the formation of both epoxy hydrazido acids and epoxy imides. The unsaturated adducts reacted with p-nitrophenyl azide to give the corresponding triazole derivatives.

  DOI：

  10.1134/s1070428007070135
• 作为产物：
  描述：

  2-[(1R,2R,6S,7R)-3,5-dioxo-4-azatricyclo[5.2.1.02,6]dec-8-en-4-ylcarbamoyl]benzoic acid 、 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride 在 溶剂黄146 作用下， 以85%的产率得到(1R,2R,6S,7R)-4-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)-4-azatricyclo[5.2.1.0^2,6]dec-8-ene-3,5-dione
  参考文献：
  名称：

  Reactions of 4-amino-4-azatricyclo[5.2.1.02,6-endo ]dec-8-ene-3,5-dione with dicarboxylic acid anhydrides

  摘要：

  Reactions of 4-amino-4-azatricyclo[5.2.1.0(2,6-endo)]dec-8-ene-3,5-dione (hydrazinolysis product of endic anhydride) with succinic, maleic, cis-cyclohexane-1,2-dicarboxylic, endic, phthalic, and 1,8-naphthalic anhydrides were studied. Procedures for the preparation of the corresponding hydrazido acids and bis-imides were proposed. Their reactions with peroxyformic acid, depending on the substrate nature, led to the formation of both epoxy hydrazido acids and epoxy imides. The unsaturated adducts reacted with p-nitrophenyl azide to give the corresponding triazole derivatives.

  DOI：

  10.1134/s1070428007070135