2-(4-phenylbut-1-yn-1-yl)quinoline-3-carbaldehyde | 1434153-25-9

• 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: 2-(4-phenylbut-1-yn-1-yl)quinoline-3-carbaldehyde
• 英文别名: 2-(4-Phenylbut-1-ynyl)quinoline-3-carbaldehyde；2-(4-phenylbut-1-ynyl)quinoline-3-carbaldehyde
• CAS: 1434153-25-9
• 化学式: C₂₀H₁₅NO
• 分子量: 285.345
• InChiKey: XGGYYKRRKMFVHC-UHFFFAOYSA-N

物化性质

• 沸点：
  501.8±45.0 °C(predicted)
• 密度：
  1.19±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  22
• 可旋转键数：
  4
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.1
• 拓扑面积：
  30
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  2-(4-phenylbut-1-yn-1-yl)quinoline-3-carbaldehyde 在 碘 、 sodium acetate 、 palladium diacetate 、 potassium carbonate 、 lithium chloride 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 0.33h， 生成 4-benzyl-1,2-di-p-tolyl-3H-pyrrolo[3,2,1-de]acridin-3-one
  参考文献：
  名称：

  Tandem Synthesis of Pyrroloacridones via [3 + 2] Alkyne Annulation/Ring-Opening with Concomitant Intramolecular Aldol Condensation

  摘要：

  An efficient cascade strategy for the direct synthesis of pyrrolo[3,2,1-de]acridones 4a-v, 5a-h from iodopyranoquinolines 2a-i by the palladium-catalyzed regioselective [3 + 2] alkyne annulation/ring-opening followed by intramolecular aldol condensation under microwave irradiation is described. The chemistry involves the in situ formation of pyrroloquinolines Y, via palladium-catalyzed selective [3 + 2] annulation of iodopyranoquinolines and internal akynes with ring-opening and successive intramolecular cross-aldol condensation. Both the symmetrical and unsymmetrical internal alkynes were reacted smoothly to provide the desired pyrroloacridones in good yields. This methodology provides the facile conversion of easily accessble iodopyranoquinoline into highly functionalized biologically important pyrroloacridones in a single process.

  DOI：

  10.1021/jo400539x

文献信息

• Triple‐Bond Directed Csp ² −N Bond Formation with <i>N</i> ‐Fluorobenzenesulfonimide as Aminating Source: One‐Step Transformation of Aldehydes into Amines
  作者：Sushmita、Trapti Aggarwal、Norio Shibata、Akhilesh K. Verma

  DOI：10.1002/chem.201903495

  日期：2019.12.13

  amination of ortho‐alkynyl quinoline/pyridine aldehydes using N‐fluorobenzenesulfonimide as nitrogen source under mild reaction conditions has been described. The designed reaction strategy was triggered by trapping of fluorine by base with subsequent attack of bis(phenylsulfonyl)‐λ2‐azane on the carbonyl carbon of a heterocycle, which was gradually converted into the corresponding amine through a Curtius

  本文描述了一种无金属，多功能的三键定向方法，该方法在温和的反应条件下，使用N-氟苯磺酰亚胺作为氮源，对邻炔基喹啉/吡啶醛进行脱羰CH-氨基化。所设计的反应策略通过用碱与双（苯基磺酰基）随后攻击-λ捕集氟的触发2 -azane上的杂环，其逐渐通过库尔提斯重排型转化成相应的胺的羰基碳。该方案提供了一步一步的方法，可将醛以高收率转化为胺。合成的胺已成功转化为生物学上重要的吡咯并喹啉/吡啶。