9-bromo-2-methoxy-7,12-dihydro-5H-indolo[3,2-d][1]benzazepin-6-one | 498557-46-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯氮卓类
• 英文名称: 9-bromo-2-methoxy-7,12-dihydro-5H-indolo[3,2-d][1]benzazepin-6-one
• CAS: 498557-46-3
• 化学式: C₁₇H₁₃BrN₂O₂
• 分子量: 357.206
• InChiKey: BDGMLSKKNBJWEY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  22
• 可旋转键数：
  1
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.12
• 拓扑面积：
  54.1
• 氢给体数：
  2
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  9-bromo-2-methoxy-7,12-dihydro-5H-indolo[3,2-d][1]benzazepin-6-one 在 三溴化硼 、 potassium carbonate 作用下， 以 二氯甲烷 、 二甲基亚砜 为溶剂， 反应 12.0h， 生成 9-bromo-2-(4-phthalimidobutoxy)-7,12-dihydroindolo[3,2-d][1]benzazepin-6(5H)-one
  参考文献：
  名称：

  Synthesis of Paullones with Aminoalkyl Side Chains

  摘要：

  Paullones 3 and 4 with aminoalkyl side chains in 2- or 3-position were synthesized as derivatives of kenpaullone 1. Both 3 and 4 showed the characteristic CDK1-inhibitory activity of the paullones and a modest antiproliferative activity on cultured human tumor cell lines. Hence, 3 and 4 appear to be suitable tools for affinity studies directed to find additional intracellular paullone targets.

  DOI：

  10.1002/1521-4184(200209)335:7<311::aid-ardp311>3.0.co;2-f
• 作为产物：
  描述：

  2-氨基-5-甲氧基苯甲酸乙酯 在 吡啶 、 sodium acetate 、 potassium hydride 作用下， 以 水 、 溶剂黄146 、 二甲基亚砜 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 11.0h， 生成 9-bromo-2-methoxy-7,12-dihydro-5H-indolo[3,2-d][1]benzazepin-6-one
  参考文献：
  名称：

  Synthesis of Paullones with Aminoalkyl Side Chains

  摘要：

  Paullones 3 and 4 with aminoalkyl side chains in 2- or 3-position were synthesized as derivatives of kenpaullone 1. Both 3 and 4 showed the characteristic CDK1-inhibitory activity of the paullones and a modest antiproliferative activity on cultured human tumor cell lines. Hence, 3 and 4 appear to be suitable tools for affinity studies directed to find additional intracellular paullone targets.

  DOI：

  10.1002/1521-4184(200209)335:7<311::aid-ardp311>3.0.co;2-f

文献信息

• Synthesis of Paullones with Aminoalkyl Side Chains
  作者：Karen Wieking、Marie Knockaert、Maryse Leost、Daniel W. Zaharevitz、Laurent Meijer、Conrad Kunick

  DOI：10.1002/1521-4184(200209)335:7<311::aid-ardp311>3.0.co;2-f

  日期：2002.9

  Paullones 3 and 4 with aminoalkyl side chains in 2- or 3-position were synthesized as derivatives of kenpaullone 1. Both 3 and 4 showed the characteristic CDK1-inhibitory activity of the paullones and a modest antiproliferative activity on cultured human tumor cell lines. Hence, 3 and 4 appear to be suitable tools for affinity studies directed to find additional intracellular paullone targets.