4-(1,3-diphenylpyrazol-4-yl)imidazo[4,5-c]pyridine | 1206607-17-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 4-(1,3-diphenylpyrazol-4-yl)imidazo[4,5-c]pyridine
• 英文别名: 4-(1,3-Diphenylpyrazol-4-yl)imidazo[4,5-c]-pyridine；4-(1,3-diphenylpyrazol-4-yl)-1H-imidazo[4,5-c]pyridine
• CAS: 1206607-17-1
• 化学式: C₂₁H₁₅N₅
• 分子量: 337.384
• InChiKey: SENRLONONHLDLI-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  26
• 可旋转键数：
  3
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  59.4
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  4-(1,3-diphenylpyrazol-4-yl)spinacine 在 sulfur 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 以33%的产率得到4-(1,3-diphenylpyrazol-4-yl)imidazo[4,5-c]pyridine
  参考文献：
  名称：

  Synthesis and dehydrogenation of spinaceamine and spinacine 4-hetaryl derivatives

  摘要：

  The reaction of histamine and histidine with various hetarylaldehydes under the conditions of the base-catalyzed Pictet-Spengler process affords 4-hetaryl-substituted derivatives of spinaceamine and spinacine. The dehydrogenation of the 4-hetaryl-substituted spinaceamine derivatives using elemental sulfur in DMF at 120-130 degrees C led to the formation of 4-hetaryl derivatives of imidazo[4,5-c]-pyridine. Under similar conditions the 4-hetaryl-substituted spinacine derivatives suffered both the dehydrogenation and oxidative decarboxylation resulting in the products identical to the compounds obtained by the dehydrogenation of 4-hetaryl-substituted spinaceamine.

  DOI：

  10.1134/s1070428009080181

文献信息

• Dehydrogenation of 4-aryl(hetaryl) spinacine derivatives with dimethyl sulfoxide
  作者：D. A. Lomov、M. G. Abramyants、N. V. Astashkina、N. I. Korotkikh、S. V. Gres’ko

  DOI：10.1134/s1070428014070185

  日期：2014.7