N⁴-(10-Methyl-2,3-dihydro-[1,4]dioxino[2,3-f]quinolin-6-yl)-pentane-1,4-diamine | 82095-10-1

• 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: N⁴-(10-Methyl-2,3-dihydro-[1,4]dioxino[2,3-f]quinolin-6-yl)-pentane-1,4-diamine
• 英文别名: 4-N-(10-methyl-2,3-dihydro-[1,4]dioxino[2,3-f]quinolin-6-yl)pentane-1,4-diamine
• CAS: 82095-10-1
• 化学式: C₁₇H₂₃N₃O₂
• 分子量: 301.389
• InChiKey: BAQIAANQWICKSC-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.5
• 重原子数：
  22
• 可旋转键数：
  5
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  69.4
• 氢给体数：
  2
• 氢受体数：
  5

反应信息

• 作为产物：
  描述：

  7-硝基-2,3-二氢-苯并[1,4]二噁英-6-胺 在 镍 磷酸 、 氢气 、 砷酸、原砷酸 、 一水合肼 、 三乙胺 作用下， 以 乙二醇乙醚 、 乙醇 为溶剂， 100.0~110.0 ℃ 、310.27 kPa 条件下， 反应 4.5h， 生成 N⁴-(10-Methyl-2,3-dihydro-[1,4]dioxino[2,3-f]quinolin-6-yl)-pentane-1,4-diamine
  参考文献：
  名称：

  Antimalarials. 13. 5-Alkoxy analogs of 4-methylprimaquine

  摘要：

  A series of nuclear and side-chain analogues of 4-methylprimaquine incorporating an alkoxy group in the 5-position of the quinoline nucleus has been prepared. The compounds were tested for suppressive antimalarial activity against Plasmodium berghei in mice and for radical curative antimalarial activity against Plasmodium cynomolgi in the rhesus monkey. Although the toxicity problems characteristic of the 8-aminoquinolines were not overcome, several of the compounds, surprisingly, were highly effective as both blood and tissue schizonticidal agents.

  DOI：

  10.1021/jm00350a016

文献信息

• Antimalarials. 13. 5-Alkoxy analogs of 4-methylprimaquine
  作者：Maurice P. LaMontagne、Anica Markovac、M. Sami Khan

  DOI：10.1021/jm00350a016

  日期：1982.8

  A series of nuclear and side-chain analogues of 4-methylprimaquine incorporating an alkoxy group in the 5-position of the quinoline nucleus has been prepared. The compounds were tested for suppressive antimalarial activity against Plasmodium berghei in mice and for radical curative antimalarial activity against Plasmodium cynomolgi in the rhesus monkey. Although the toxicity problems characteristic of the 8-aminoquinolines were not overcome, several of the compounds, surprisingly, were highly effective as both blood and tissue schizonticidal agents.