phenyl(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)methanol | 59563-79-0

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 唑类
• 英文名称: phenyl(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)methanol
• 英文别名: phenyl-(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-methanol；Phenyl-<1-phenyl-1H-pyrazolo<3,4-d>pyrimidin-4-yl>-methanol；Phenyl-(1-phenylpyrazolo[3,4-d]pyrimidin-4-yl)methanol
• CAS: 59563-79-0
• 化学式: C₁₈H₁₄N₄O
• 分子量: 302.335
• InChiKey: ULXOGDJGULLAPC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.7
• 重原子数：
  23
• 可旋转键数：
  3
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  63.8
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  4-氯-1-苯基-1H-吡唑并[3,4-d]嘧啶 在 正丁基锂 作用下， 以 四氢呋喃 为溶剂， 生成 phenyl(1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-4-yl)methanol
  参考文献：
  名称：

  Lithiation of 1H-pyrazolo[3,4-d]pyrimidine derivative using lithium alkanetellurolate

  摘要：

  4-Chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine was converted into alkyl 1-phenyl-1H-pyrazolo[3,4-d] pyrimidin-4-yl telluride, which was lithiated using alkyllithium followed by the reaction with electrophiles. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4039(99)00132-x

文献信息

• The tellurium–lithium exchange reaction: selective functionalization of electron-deficient heteroaromatics
  作者：Osamu Sugimoto、Muneyoshi Sudo、Ken-ichi Tanji

  DOI：10.1016/s0040-4020(01)00089-8

  日期：2001.3

  Electron-deficient heteroaromatic tellurides, which was obtained from the corresponding haloheteroaromatics, reacted selectively with n-butyllithium to give the lithio derivatives. (C) 2001 Elsevier Science Ltd. All rights reserved.
• HIGASHINO T.; GOI M.; HAYASHI E., CHEM. AND PHARM. BULL. <CPBT-AL>, 1976, 24, NO 2, 238-252
  作者：HIGASHINO T.、 GOI M.、 HAYASHI E.

  DOI：——

  日期：——
• Lithiation of 1H-pyrazolo[3,4-d]pyrimidine derivative using lithium alkanetellurolate
  作者：Osamu Sugimoto、Muneyoshi Sudo、Ken-ichi Tanji

  DOI：10.1016/s0040-4039(99)00132-x

  日期：1999.3

  4-Chloro-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine was converted into alkyl 1-phenyl-1H-pyrazolo[3,4-d] pyrimidin-4-yl telluride, which was lithiated using alkyllithium followed by the reaction with electrophiles. (C) 1999 Elsevier Science Ltd. All rights reserved.