3-cyano-6-phenyl-5-phenylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one | 1237748-38-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: 3-cyano-6-phenyl-5-phenylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one
• CAS: 1237748-38-7
• 化学式: C₂₅H₁₈N₆O
• 分子量: 418.458
• InChiKey: BOFLJWJRAKYRFC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  32.0
• 可旋转键数：
  4.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.04
• 拓扑面积：
  88.53
• 氢给体数：
  1.0
• 氢受体数：
  7.0

反应信息

• 作为产物：
  描述：

  、 苯胺 以 二氯甲烷 为溶剂， 反应 8.0h， 生成 3-cyano-6-phenyl-5-phenylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-one
  参考文献：
  名称：

  Regiospecific synthesis of 6-aryl-3-cyano-5-alkylamino/arylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-ones via iminophosphorane-mediated annulation

  摘要：

  An efficient and straightforward approach to the synthesis of 6-aryl-3-cyano-5-alkylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-ones 8 has been developed from the readily commercially available starting materials 4-methylaniline and malononitrile in five steps. The key to the pyrazolo[4, 3-d]pyrimidin-7(6H)-ones relies on an iminophosphorane-mediated annulation, followed by a nucleophilic addition with amines. The structures of the title compounds are clearly characterized by IR, H-1 NMR, MS, elemental analysis or X-ray diffraction crystallography. Published by Elsevier Ltd.

  DOI：

  10.1016/j.tet.2010.04.114

文献信息

• Regiospecific synthesis of 6-aryl-3-cyano-5-alkylamino/arylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-ones via iminophosphorane-mediated annulation
  作者：Ming-Hu Wu、Ji-Huan Hu、Dong-Sheng Shen、Paul Brémond、Haibing Guo

  DOI：10.1016/j.tet.2010.04.114

  日期：2010.7

  An efficient and straightforward approach to the synthesis of 6-aryl-3-cyano-5-alkylamino-1-p-tolyl-1H-pyrazolo[4,3-d]pyrimidin-7(6H)-ones 8 has been developed from the readily commercially available starting materials 4-methylaniline and malononitrile in five steps. The key to the pyrazolo[4, 3-d]pyrimidin-7(6H)-ones relies on an iminophosphorane-mediated annulation, followed by a nucleophilic addition with amines. The structures of the title compounds are clearly characterized by IR, H-1 NMR, MS, elemental analysis or X-ray diffraction crystallography. Published by Elsevier Ltd.