(E)-N-{3-[4-(2-oxo-2-(pyrrolidin-1-yl)ethyl)phenyl]allyl}-1H-pyrrolo[3,4-b]quinolin-3(2H)-one | 1370636-20-6

• 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: (E)-N-{3-[4-(2-oxo-2-(pyrrolidin-1-yl)ethyl)phenyl]allyl}-1H-pyrrolo[3,4-b]quinolin-3(2H)-one
• 英文别名: 2-[(E)-3-[4-(2-oxo-2-pyrrolidin-1-ylethyl)phenyl]prop-2-enyl]-1H-pyrrolo[3,4-b]quinolin-3-one
• CAS: 1370636-20-6
• 化学式: C₂₆H₂₅N₃O₂
• 分子量: 411.503
• InChiKey: KSTLYYKGFUEUHO-AATRIKPKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  31
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.27
• 拓扑面积：
  53.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为产物：
  描述：

  1-(二甲氧基甲基)-2-氨基苯 在 palladium diacetate 、 1-羟基苯并三唑 、 caesium carbonate 、 对甲苯磺酸 、 盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺 、 N,N-二异丙基乙胺 、 三苯基膦 作用下， 以 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 40.0h， 生成 (E)-N-{3-[4-(2-oxo-2-(pyrrolidin-1-yl)ethyl)phenyl]allyl}-1H-pyrrolo[3,4-b]quinolin-3(2H)-one
  参考文献：
  名称：

  Synthesis of novel building blocks of 1H-pyrrolo[3,4-b]quinolin-3(2H)-one and evaluation of their antitumor activity

  摘要：

  A series of new building blocks consisting of 1H-pyrrolo[3,4-b]quinolin-3(2H)-one with potential as selective antitumor agents is described. Compounds were synthesized by using Heck reaction of N-allyl-1H-pyrrolo[3,4-b]quinolin-3(2H)-one with p-bromophenyl acetic acid followed by formation of amide (1a-h, 2a-d) by reaction with several secondary amines in good yields. The cytotoxicity of these compounds was evaluated against human cancer cell lines in vitro (SK-N-NH, A549). Studies suggest that most of these compounds were effective in inhibiting neuroblastoma cell growth, compound 1d was the most potent one (% IC50 = 8.62 mu M).

  DOI：

  10.1007/s00044-012-0018-x

文献信息

• Synthesis of novel building blocks of 1H-pyrrolo[3,4-b]quinolin-3(2H)-one and evaluation of their antitumor activity
  作者：Lingaiah Nagarapua、Hanmant K. Gaikwad、Sheeba Rani Manikonda、Rajashaker Bantu、Krishna Madhuri Manda、Shasi Vardhan Kalivendi

  DOI：10.1007/s00044-012-0018-x

  日期：2013.1

  A series of new building blocks consisting of 1H-pyrrolo[3,4-b]quinolin-3(2H)-one with potential as selective antitumor agents is described. Compounds were synthesized by using Heck reaction of N-allyl-1H-pyrrolo[3,4-b]quinolin-3(2H)-one with p-bromophenyl acetic acid followed by formation of amide (1a-h, 2a-d) by reaction with several secondary amines in good yields. The cytotoxicity of these compounds was evaluated against human cancer cell lines in vitro (SK-N-NH, A549). Studies suggest that most of these compounds were effective in inhibiting neuroblastoma cell growth, compound 1d was the most potent one (% IC50 = 8.62 mu M).