(2S)-2-((E)-2-(4-trifluoromethylphenyl)vinyl)piperidine | 1565872-65-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: (2S)-2-((E)-2-(4-trifluoromethylphenyl)vinyl)piperidine
• 英文别名: (2S)-2-[(E)-2-[4-(trifluoromethyl)phenyl]ethenyl]piperidine
• CAS: 1565872-65-2
• 化学式: C₁₄H₁₆F₃N
• 分子量: 255.283
• InChiKey: SCERKYLBVGCZDI-PPGNKHEKSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.7
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  12
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  1-Boc-哌啶 在 lithium aluminium tetrahydride 、 四丁基溴化铵 、 仲丁基锂 、 palladium diacetate 、 三乙胺 、 1,3-二-叔丁基咪唑氯化物 、 (+)-鹰爪豆碱 作用下， 以 四氢呋喃 、 乙醚 、 乙醇 、 水 为溶剂， 反应 14.08h， 生成 (2S)-2-((E)-2-(4-trifluoromethylphenyl)vinyl)piperidine
  参考文献：
  名称：

  Pd- N -heterocyclic carbene catalyzed synthesis of piperidine alkene–alkaloids and their anti-cancer evaluation

  摘要：

  A facile synthesis of piperidine alkene-alkaloids including natural (+)-Caulophyllumine B in high yields has been developed by Heck cross-coupling reaction catalyzed by simple in situ formed palladium-N-heterocyclic carbenes (Pd-NHCs). Formation of Pd(0) nanoparticles has been noticed during the reaction course. The synthesized piperidine alkene-alkaloids were evaluated for in vitro anti-cancer activity against a panel of human tumor cell lines of lung, breast and ovarian. Several of these piperidine alkene-alkaloids were found to possess highest growth inhibition activity than the standard drug cisplatin and support the concept to modulate drug receptor interaction. (C) 2013 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmcl.2013.12.108

文献信息

• Pd- N -heterocyclic carbene catalyzed synthesis of piperidine alkene–alkaloids and their anti-cancer evaluation
  作者：Shravankumar Kankala、Ranjith Kumar Kankala、Ramesh Balaboina、Narasimha Swamy Thirukovela、Ravinder Vadde、Chandra Sekhar Vasam

  DOI：10.1016/j.bmcl.2013.12.108

  日期：2014.2

  A facile synthesis of piperidine alkene-alkaloids including natural (+)-Caulophyllumine B in high yields has been developed by Heck cross-coupling reaction catalyzed by simple in situ formed palladium-N-heterocyclic carbenes (Pd-NHCs). Formation of Pd(0) nanoparticles has been noticed during the reaction course. The synthesized piperidine alkene-alkaloids were evaluated for in vitro anti-cancer activity against a panel of human tumor cell lines of lung, breast and ovarian. Several of these piperidine alkene-alkaloids were found to possess highest growth inhibition activity than the standard drug cisplatin and support the concept to modulate drug receptor interaction. (C) 2013 Elsevier Ltd. All rights reserved.