11,12-dihydro-9-hydroxy-8-methoxy-2,3-methylenedioxybenzo[c]phenanthridine | 1581303-15-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 11,12-dihydro-9-hydroxy-8-methoxy-2,3-methylenedioxybenzo[c]phenanthridine
• CAS: 1581303-15-2
• 化学式: C₁₉H₁₅NO₄
• 分子量: 321.332
• InChiKey: ZMECPVCPJQILPZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.44
• 重原子数：
  24.0
• 可旋转键数：
  1.0
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  60.81
• 氢给体数：
  1.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  11,12-dihydro-9-hydroxy-8-methoxy-2,3-methylenedioxybenzo[c]phenanthridine 在 Jones reagent 、 palladium 10% on activated carbon 作用下， 以 邻二氯苯 、 丙酮 为溶剂， 反应 20.0h， 生成 isoterihanine chloride
  参考文献：
  名称：

  Total Synthesis of the Benzo[c]phenanthridine Alkaloids, Terihanine and Isoterihanine, and Their Antitumor Activity

  摘要：

  A new total synthesis of terihanine (2a) and isoterihanine (2b) was established by our new bond formation between the C4b and N5 positions of the benzo[c]phenanthridine ring based on a microwave-assisted thermal electrocyclic reaction of 2-cycloalkenylbenzaldoxime as an aza 6 pi-electron system. In addition, the antitumor activity of these synthesized compounds, including nitidine and nornitidine was evaluated in HCT-116 cells.

  DOI：

  10.3987/com-13-s(s)16
• 作为产物：
  描述：

  2-(3,4-dihydro-6,7-methylenedioxy-2-naphthyl)-4-hydroxy-5-methoxybenzaldehyde 在 sodium acetate 作用下， 以 乙醇 、 邻二氯苯 为溶剂， 反应 8.0h， 生成 11,12-dihydro-9-hydroxy-8-methoxy-2,3-methylenedioxybenzo[c]phenanthridine
  参考文献：
  名称：

  Total Synthesis of the Benzo[c]phenanthridine Alkaloids, Terihanine and Isoterihanine, and Their Antitumor Activity

  摘要：

  A new total synthesis of terihanine (2a) and isoterihanine (2b) was established by our new bond formation between the C4b and N5 positions of the benzo[c]phenanthridine ring based on a microwave-assisted thermal electrocyclic reaction of 2-cycloalkenylbenzaldoxime as an aza 6 pi-electron system. In addition, the antitumor activity of these synthesized compounds, including nitidine and nornitidine was evaluated in HCT-116 cells.

  DOI：

  10.3987/com-13-s(s)16