4-hydrazino-3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine | 1146953-48-1

• 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-hydrazino-3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine
• 英文别名: 4-Hydrazino-3,6-dimethyl-1-phenyl-1h-pyrazolo[3,4-d]-pyrimidine；(3,6-dimethyl-1-phenylpyrazolo[3,4-d]pyrimidin-4-yl)hydrazine
• CAS: 1146953-48-1
• 化学式: C₁₃H₁₄N₆
• 分子量: 254.294
• InChiKey: RIIOAUDOOMUUJZ-UHFFFAOYSA-N

物化性质

• 熔点：
  225-227 °C(Solvent: Ethanol)
• 沸点：
  472.4±47.0 °C(predicted)
• 密度：
  1.40±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.2
• 重原子数：
  19
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  81.6
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  4-hydrazino-3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine 、 原丙酸三乙酯 在 sulfuric acid on silica gel 作用下， 以 乙醇 为溶剂， 反应 0.13h， 以89%的产率得到3-ethyl-5,9-dimethyl-7-phenyl-7H-pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidine
  参考文献：
  名称：

  Davoodnia, Asian Journal of Chemistry, 2010, vol. 22, # 2, p. 1595 - 1598

  摘要：

  DOI：
• 作为产物：
  描述：

  4-chloro-3,4-dimethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine 在 一水合肼 作用下， 反应 10.0h， 以89%的产率得到4-hydrazino-3,6-dimethyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine
  参考文献：
  名称：

  Synthesis of pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidines

  摘要：

  Starting from 1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-ones, a synthesis pathway to the tricyclic pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidines is described. Reaction of 1,5-dihydro-4H-pyrazolo[3,4-d] pyrimidin-4-ones with phosphoryl chloride afforded the corresponding 4-chloro-1H-pyrazolo[3,4-d]pyrimidines. Treatment of these compounds with hydrazine hydrate at reflux temperature gave the hydrazino derivatives, which were subsequently cyclized to the titled compounds on heating with orthoesters in ethanol.

  DOI：

  10.1007/s00706-008-0939-8

文献信息

• Synthesis of pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidines
  作者：Abolghasem Davoodnia、Rahele Zhiani、Niloofar Tavakoli-Hoseini

  DOI：10.1007/s00706-008-0939-8

  日期：2008.11

  Starting from 1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-ones, a synthesis pathway to the tricyclic pyrazolo[4,3-e][1,2,4]triazolo[4,3-c]pyrimidines is described. Reaction of 1,5-dihydro-4H-pyrazolo[3,4-d] pyrimidin-4-ones with phosphoryl chloride afforded the corresponding 4-chloro-1H-pyrazolo[3,4-d]pyrimidines. Treatment of these compounds with hydrazine hydrate at reflux temperature gave the hydrazino derivatives, which were subsequently cyclized to the titled compounds on heating with orthoesters in ethanol.
• Davoodnia, Asian Journal of Chemistry, 2010, vol. 22, # 2, p. 1595 - 1598
  作者：Davoodnia

  DOI：——

  日期：——