1-(4-(2-methoxyphenyl)piperazin-1-yl)-3-(6-nitrobenzo[d][1,3]dioxol-5-yl)propan-1-one | 1489128-58-6

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪烷类
• 英文名称: 1-(4-(2-methoxyphenyl)piperazin-1-yl)-3-(6-nitrobenzo[d][1,3]dioxol-5-yl)propan-1-one
• 英文别名: 1-[4-(2-Methoxyphenyl)piperazin-1-yl]-3-(6-nitro-1,3-benzodioxol-5-yl)propan-1-one；1-[4-(2-methoxyphenyl)piperazin-1-yl]-3-(6-nitro-1,3-benzodioxol-5-yl)propan-1-one
• CAS: 1489128-58-6
• 化学式: C₂₁H₂₃N₃O₆
• 分子量: 413.43
• InChiKey: NXSXWNJZRWXWLJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  30
• 可旋转键数：
  5
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.38
• 拓扑面积：
  97.1
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  3-[3,4-(亚甲二氧基)苯基]丙酸 在 吡啶 、 氯化亚砜 、 硝酸 、 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 5.5h， 生成 1-(4-(2-methoxyphenyl)piperazin-1-yl)-3-(6-nitrobenzo[d][1,3]dioxol-5-yl)propan-1-one
  参考文献：
  名称：

  New orally effective 3-(2-nitro)phenylpropanamide analgesic derivatives: Synthesis and antinociceptive evaluation

  摘要：

  A series of substituted 6-nitrophenylpropanamide derivatives (1-20) were synthesized using either the TDAE strategy or classical organic reactions. All these compounds were characterized by fusion point, 1H NMR,13C NMR, elemental analysis or mass spectrometry data. Because of their structural analogy with recently published compounds possessing antinociceptive properties, our derivatives were screened for peripheral analgesic activities on acetic acid-induced writhing in mice. Compound 13 showed the best result at 100 junol/kg ip (50% inhibition vs 59% for aspirin). This antinociceptive activity was maintained after oral administration (40% inhibition vs 31.6% for aspirin). Both hot-plate and actimetry-based tests were non-significant suggesting the analgesic activity of 13 linked to a peripheral mechanism. (C) 2013 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2013.08.041