{5-Methoxy-13-[2,2,2-trifluoro-eth-(E)-ylidene]-11-trifluoromethyl-6-aza-tricyclo[7.3.1.02,7]trideca-2(7),3,5,10-tetraen-1-yl}-carbamic acid methyl ester | 182681-20-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: {5-Methoxy-13-[2,2,2-trifluoro-eth-(E)-ylidene]-11-trifluoromethyl-6-aza-tricyclo[7.3.1.02,7]trideca-2(7),3,5,10-tetraen-1-yl}-carbamic acid methyl ester
• CAS: 182681-20-5
• 化学式: C₁₈H₁₆F₆N₂O₃
• 分子量: 422.327
• InChiKey: PGJTXGVRNLVMMN-XYOKQWHBSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.19
• 重原子数：
  29.0
• 可旋转键数：
  2.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.44
• 拓扑面积：
  60.45
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  {5-Methoxy-13-[2,2,2-trifluoro-eth-(E)-ylidene]-11-trifluoromethyl-6-aza-tricyclo[7.3.1.02,7]trideca-2(7),3,5,10-tetraen-1-yl}-carbamic acid methyl ester 在 甲醇 、 碘代三甲硅烷 作用下， 生成 (13E)-1-amino-13-(2,2,2-trifluoroethylidene)-11-(trifluoromethyl)-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one
  参考文献：
  名称：

  Synthesis and acetylcholinesterase inhibitory activity of fluorinated analogues of huperzine A

  摘要：

  Three novel fluorinated analogues of huperzine A ( 1 ), (+/-)-12, 12, 12-trifluorohuperzine A ( 2 ), (+/-)-14,14,14-trifluorohuperzine A ( 3 ), and (+/-)-12,12,12,14,14,14-hexafluorohuperzine A ( 4 ), have been synthesized by employing TMSCF(3) as a trifluoromethylating agent. These analogues were found to still retain anti-acetylcholinesterase activity. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00337-x
• 作为产物：
  描述：

  5-Methoxy-11-oxo-13-[2,2,2-trifluoro-eth-(E)-ylidene]-6-aza-tricyclo[7.3.1.02,7]trideca-2(7),3,5-triene-1-carboxylic acid methyl ester 在 四丁基氟化铵 作用下， 生成 {5-Methoxy-13-[2,2,2-trifluoro-eth-(E)-ylidene]-11-trifluoromethyl-6-aza-tricyclo[7.3.1.02,7]trideca-2(7),3,5,10-tetraen-1-yl}-carbamic acid methyl ester
  参考文献：
  名称：

  Synthesis and acetylcholinesterase inhibitory activity of fluorinated analogues of huperzine A

  摘要：

  Three novel fluorinated analogues of huperzine A ( 1 ), (+/-)-12, 12, 12-trifluorohuperzine A ( 2 ), (+/-)-14,14,14-trifluorohuperzine A ( 3 ), and (+/-)-12,12,12,14,14,14-hexafluorohuperzine A ( 4 ), have been synthesized by employing TMSCF(3) as a trifluoromethylating agent. These analogues were found to still retain anti-acetylcholinesterase activity. Copyright (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00337-x