ethyl 3-ferrocenyl-1-vinyl-1H-pyrazole-5-carboxylate | 1025324-06-4

• 英文名称: ethyl 3-ferrocenyl-1-vinyl-1H-pyrazole-5-carboxylate
• CAS: 1025324-06-4
• 化学式: C₁₈H₁₈FeN₂O₂
• 分子量: 350.2
• InChiKey: DYHZNMDVISKQQA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  None
• 重原子数：
  None
• 可旋转键数：
  None
• 环数：
  None
• sp3杂化的碳原子比例：
  None
• 拓扑面积：
  None
• 氢给体数：
  None
• 氢受体数：
  None

反应信息

• 作为产物：
  描述：

  ethyl-1-(2-bromoethyl)-3-ferrocenyl-1H-pyrazole-5-carboxylate 、 苄胺 在 triethylamine 作用下， 以 乙腈 为溶剂， 生成 ethyl 3-ferrocenyl-1-vinyl-1H-pyrazole-5-carboxylate 、 5-benzyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one
  参考文献：
  名称：

  Synthesis, structure characterization and preliminary biological evaluation of novel 5-alkyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives

  摘要：

  A series of novel 5-alkyl-2-ferrocenyl-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one derivatives were synthesized by the reaction of ethyl 1-(2-bromoethyl)-3-ferrocenyl-1H-pyrazole-5-carboxylate with non-aromatic primary amines in one-pot procedure and characterized by H-1 NMR, C-13 NMR, IR, HRMS and X-ray diffraction analysis. The effects of all the compounds on A549 cell growth were investigated. The results showed that all compounds had almost inhibitory effects on the growth of A549 cells. (c) 2008 Elsevier B. V. All rights reserved.

  DOI：

  10.1016/j.jorganchem.2008.01.043