1-(2-methylallyl)quinolin-4(1H)-one | 1206-82-2

• 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: 1-(2-methylallyl)quinolin-4(1H)-one
• 英文别名: 1-(2-Methylallyl)quinolin-4-one；1-(2-methylprop-2-enyl)quinolin-4-one
• CAS: 1206-82-2
• 化学式: C₁₃H₁₃NO
• 分子量: 199.252
• InChiKey: JUEVAUOJUBUOJY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  15
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.15
• 拓扑面积：
  20.3
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  1-(2-methylallyl)quinolin-4(1H)-one 在 N-溴代丁二酰亚胺(NBS) 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以98%的产率得到N-(2-methylallyl)-3-bromo-4-quinolone
  参考文献：
  名称：

  Synthesis of halogenated 4-quinolones and evaluation of their antiplasmodial activity

  摘要：

  Treatment of 4-hydroxyquinolines with (2-methyl) allyl bromide in the presence of K2CO3 resulted in the formation of novel N-[(2-methyl) allyl]-4-quinolones through selective N-alkylation. Further reaction of N-(2-methylallyl)-4-quinolones with bromine or N-bromosuccinimide yielded the corresponding 3-bromo- 1-(2,3-dibromo-2-methylpropyl)-4-quinolones and 3-bromo-1-(2-methylallyl)-4-quinolones, respectively. Furthermore, a copper-catalyzed C-N coupling of the latter 3-bromo-4-quinolones with (5-chloro) indole afforded novel 3-[(5-chloro) indol-1-yl]-4-quinolone hybrids. Antifungal and antiplasmodial assays of all new 4-quinolones were performed and revealed no antifungal properties but moderate antiplasmodial activities. All 15 compounds displayed micromolar activities against a chloroquine- sensitive strain of Plasmodium falciparum, and the five most potent compounds also showed micromolar activities against a chloroquine-resistant strain of P. falciparum with IC50-values ranging between 4 and 70 mu M. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.12.067
• 作为产物：
  描述：

  3-溴-2-甲基丙烯 、 1,4-dihydroquinolin-4-ol 在 potassium carbonate 作用下， 以 丙酮 为溶剂， 反应 24.0h， 以79%的产率得到1-(2-methylallyl)quinolin-4(1H)-one
  参考文献：
  名称：

  Synthesis of halogenated 4-quinolones and evaluation of their antiplasmodial activity

  摘要：

  Treatment of 4-hydroxyquinolines with (2-methyl) allyl bromide in the presence of K2CO3 resulted in the formation of novel N-[(2-methyl) allyl]-4-quinolones through selective N-alkylation. Further reaction of N-(2-methylallyl)-4-quinolones with bromine or N-bromosuccinimide yielded the corresponding 3-bromo- 1-(2,3-dibromo-2-methylpropyl)-4-quinolones and 3-bromo-1-(2-methylallyl)-4-quinolones, respectively. Furthermore, a copper-catalyzed C-N coupling of the latter 3-bromo-4-quinolones with (5-chloro) indole afforded novel 3-[(5-chloro) indol-1-yl]-4-quinolone hybrids. Antifungal and antiplasmodial assays of all new 4-quinolones were performed and revealed no antifungal properties but moderate antiplasmodial activities. All 15 compounds displayed micromolar activities against a chloroquine- sensitive strain of Plasmodium falciparum, and the five most potent compounds also showed micromolar activities against a chloroquine-resistant strain of P. falciparum with IC50-values ranging between 4 and 70 mu M. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.12.067

文献信息

• Synergistic Organoboron/Palladium Catalysis for Regioselective N-Allylation of 2-Pyridones, 4-Pyridones, and Related Ambident Heterocycles
  作者：Mark S. Taylor、Giorgos Yatzoglou、Matthew T. Zambri、Shrey P. Desai

  DOI：10.1055/s-0043-1763618

  日期：2024.5

  The use of a boronic acid co-catalyst along with a palladium complex enables efficient dehydrative couplings of allylic alcohols and tautomerizable heterocycles. The protocol has been applied to achieve N-allylations of 2-pyridones, 4-pyridones, 4-pyrimidinones, and their benzofused derivatives.

  硼酸助催化剂与钯络合物的使用能够实现烯丙醇和可互变杂环的有效脱水偶联。该方案已用于实现 2-吡啶酮、4-吡啶酮、4-嘧啶酮及其苯并稠合衍生物的 N-烯丙基化。
• Direct Synthesis of N‐Alkyl‐2‐Pyridones Using 2‐Halogenated Pyridines
  作者：Xia Chen、Jianyi Shi、Yuqun Lin、Yibiao Li、Shaohua Jiang、Tianxiang Chen、Zhongzhi Zhu、Aijun Ma

  DOI：10.1002/ejoc.202301184

  日期：2024.2.12

  This study presents a method for synthesizing pyridine, quinoline, and isoquinoline ketones from 2-halogenated N-heterocycles under mild conditions. The use of H2O as both solvent and oxygen source makes the reaction environmentally friendly, with broad substrate applicability and high functional group tolerance.

  本研究提出了一种在温和条件下从 2-卤代 N-杂环合成吡啶、喹啉和异喹啉酮的方法。使用H 2 O作为溶剂和氧源使反应环境友好，具有广泛的底物适用性和高官能团耐受性。
• Synthesis of halogenated 4-quinolones and evaluation of their antiplasmodial activity
  作者：Stéphanie Vandekerckhove、Tom Desmet、Hai Giang Tran、Carmen de Kock、Peter J. Smith、Kelly Chibale、Matthias D’hooghe

  DOI：10.1016/j.bmcl.2013.12.067

  日期：2014.2

  Treatment of 4-hydroxyquinolines with (2-methyl) allyl bromide in the presence of K2CO3 resulted in the formation of novel N-[(2-methyl) allyl]-4-quinolones through selective N-alkylation. Further reaction of N-(2-methylallyl)-4-quinolones with bromine or N-bromosuccinimide yielded the corresponding 3-bromo- 1-(2,3-dibromo-2-methylpropyl)-4-quinolones and 3-bromo-1-(2-methylallyl)-4-quinolones, respectively. Furthermore, a copper-catalyzed C-N coupling of the latter 3-bromo-4-quinolones with (5-chloro) indole afforded novel 3-[(5-chloro) indol-1-yl]-4-quinolone hybrids. Antifungal and antiplasmodial assays of all new 4-quinolones were performed and revealed no antifungal properties but moderate antiplasmodial activities. All 15 compounds displayed micromolar activities against a chloroquine- sensitive strain of Plasmodium falciparum, and the five most potent compounds also showed micromolar activities against a chloroquine-resistant strain of P. falciparum with IC50-values ranging between 4 and 70 mu M. (C) 2013 Elsevier Ltd. All rights reserved.