5-bromo-4-(4-naphthalen-2-yl-6-phenyl-1,3,5-triazin-2-yl)pyridin-3-ol | 1616763-37-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 5-bromo-4-(4-naphthalen-2-yl-6-phenyl-1,3,5-triazin-2-yl)pyridin-3-ol
• CAS: 1616763-37-1
• 化学式: C₂₄H₁₅BrN₄O
• 分子量: 455.313
• InChiKey: MMRHUWYNMDMJDA-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.89
• 重原子数：
  30.0
• 可旋转键数：
  3.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  71.79
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为产物：
  描述：

  5-bromo-2-(naphthalen-2-yl)-4H-pyrido[4,3-e][1,3]oxazin-4-one 、 苯甲脒 以 乙醇 为溶剂， 反应 0.17h， 以55%的产率得到5-bromo-4-(4-naphthalen-2-yl-6-phenyl-1,3,5-triazin-2-yl)pyridin-3-ol
  参考文献：
  名称：

  Access to Pyridyl-Substituted 1,3,5-Triazines from 4H-Pyrido[1,3]oxazin-4-ones via a Cyclocondensation Process

  摘要：

  Pyridyl-substituted 1,3,5-triazines were synthesized in good to excellent yields via an unprecedented one-step cyclocondensation of 4H-pyrido[1,3]oxazin-4-ones with amidines at room temperature or under microwave irradiations. The broad applicability was demonstrated by 33 examples with a variety of amidines and three different 4H-pyrido[1,3]oxazin-4-one chemical series. In addition, a one-pot process from 4H-pyrido[1,3]oxazin-4-one precursors (imide sodium salts) was developed and led to the desired triazines compounds, thus allowing a one-step economy in their global synthetic preparation. This approach provides rapid access to pyridyl (or pyridone)-substituted 1,3,5-triazines with high potential in various fields of application.

  DOI：

  10.1021/jo5010668