8-fluoro-N-phenylpyrimido[4,5-b][1,4]benzoxazepin-4-amine | 875925-97-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶嗪类
• 英文名称: 8-fluoro-N-phenylpyrimido[4,5-b][1,4]benzoxazepin-4-amine
• CAS: 875925-97-6
• 化学式: C₁₇H₁₁FN₄O
• 分子量: 306.299
• InChiKey: ZBGYUDMCRFFQLC-UHFFFAOYSA-N

物化性质

• 沸点：
  490.5±45.0 °C(Predicted)
• 密度：
  1.38±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.22
• 重原子数：
  23.0
• 可旋转键数：
  2.0
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  59.4
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  8-fluoro-N-phenylpyrimido[4,5-b][1,4]benzoxazepin-4-amine 在 sodium tetrahydroborate 、 乙醇 作用下， 生成 (8-Fluoro-10,11-dihydro-5-oxa-2,4,11-triaza-dibenzo[a,d]cyclohepten-1-yl)-phenyl-amine
  参考文献：
  名称：

  Microwave-assisted three component one-pot synthesis of pyrimido-oxazepines

  摘要：

  A synthetic approach toward pyrimido-oxazepine analogs was developed through the use of microwave heating. Certain analogs can be made in one step, which make this a valuable tool in the investigation of this therapeutically relevant scaffold. (c) 2007 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tetlet.2006.12.058
• 作为产物：
  描述：

  6-氯-N4-苯基-4,5-嘧啶二胺 、 5-氟水杨醛 在 sodium hydride 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 生成 8-fluoro-N-phenylpyrimido[4,5-b][1,4]benzoxazepin-4-amine
  参考文献：
  名称：

  Tricyclic azepine derivatives: Pyrimido[4,5-b]-1,4-benzoxazepines as a novel class of epidermal growth factor receptor kinase inhibitors

  摘要：

  A novel class of pyrimido[4,5-b]-1,4-benzoxazepines is described as inhibitors of epidermal growth factor receptor (EGFR) tyrosine kinase. Two compounds display potent EGFR inhibitory activity of less than 1 mu M in cellular phosphorylation assays (IC50 0.47-0.69 mu M) and are highly selective against a small kinase panel. Such compounds demonstrate anti-EGFR activity within a class that is different from any known EGFR inhibitor scaffolds. They also provide a basis for the design of kinase inhibitors with the desired selectivity profile. (C) 2005 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2005.12.018