2-(3-nitrobenzylidene)-3-oxo-N-phenylbutanamide | 1101202-84-9

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 肉桂酸及其衍生物
• 英文名称: 2-(3-nitrobenzylidene)-3-oxo-N-phenylbutanamide
• CAS: 1101202-84-9
• 化学式: C₁₇H₁₄N₂O₄
• 分子量: 310.309
• InChiKey: PAGIMLYNIWTYOR-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.21
• 重原子数：
  23.0
• 可旋转键数：
  5.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.06
• 拓扑面积：
  89.31
• 氢给体数：
  1.0
• 氢受体数：
  4.0

反应信息

• 作为反应物：
  描述：

  2-(3-nitrobenzylidene)-3-oxo-N-phenylbutanamide 在 potassium carbonate 作用下， 以 乙醇 为溶剂， 反应 12.0h， 生成
  参考文献：
  名称：

  Synthesis, structural characterization and biological studies of copper complexes with 2-aminobenzothiazole derivatives

  摘要：

  Novel copper complexes of 2-aminobenzothiazole derivatives were synthesized by the condensation of Knoevenagel condensate acetoacetanilide (obtained from substituted benzaldehydes and acetoacetanilide) and 2-aminobenzothiazole. They were thoroughly characterized by elemental analysis, IR, H-1 NMR, UV-Vis., MS Spectra, molar conductance, magnetic moment and electrochemical studies. These spectral studies suggested that distorted square planar geometry for all the complexes. Molar conductance data and magnetic susceptibility measurements provide evidence for monomeric and neutral nature of the complexes. The electrochemical behaviour of the ligand and complexes in DMSO at 298 K was studied. The present ligand systems stabilize the unusual oxidation states of copper ion during electrolysis. Antibacterial screening of the ligands and their complexes reveal that all the complexes show higher activities than the free ligands. (C) 2014 Elsevier B.V. All rights reserved.

  DOI：

  10.1016/j.molstruc.2014.01.028
• 作为产物：
  描述：

  间硝基苯甲醛 、 N-乙酰乙酰苯胺 在 哌啶 、 溶剂黄146 作用下， 生成 2-(3-nitrobenzylidene)-3-oxo-N-phenylbutanamide
  参考文献：
  名称：

  Triflic酸酐促进N-芳基肉桂酸酯的分子内环化：访问多取代的喹啉2（1H）-一。

  摘要：

  摘要 通过在温和的条件下在N，N-二甲基三氟乙酰胺（DTA）中由三氟甲磺酸酐促进的易于获得的N-芳基肉桂酸酯的分子内环化作用，开发了一种简便，有效的多取代喹啉2（1 H）-酮合成方法。 通过在温和的条件下在N，N-二甲基三氟乙酰胺（DTA）中由三氟甲磺酸酐促进的易于获得的N-芳基肉桂酸酯的分子内环化作用，开发了一种简便，有效的多取代喹啉2（1 H）-酮合成方法。

  DOI：

  10.1055/s-0036-1590821

文献信息

• Synthesis and 3D-QSAR study of 1,4-dihydropyridine derivatives as MDR cancer reverters
  作者：Ashish Radadiya、Vijay Khedkar、Abhay Bavishi、Hardevsinh Vala、Shailesh Thakrar、Dhairya Bhavsar、Anamik Shah、Evans Coutinho

  DOI：10.1016/j.ejmech.2014.01.011

  日期：2014.3

  A series of symmetrical and unsymmetrical 1,4-dihydropyridines were synthesized by a rapid, single pot microwave irradiation (MWI) based protocol along with conventional approach and characterized by NMR, IR and mass spectroscopic techniques. The compounds were evaluated for their tumor cell cytotoxicity in HL-60 tumor cells. A 3D-QSAR study using CoMFA and CoMSIA was carried out to decipher the factors governing MDR reversing ability in cancer. The resulting contour maps derived by the best 3D-QSAR models provide a good insight into the molecular features relevant to the biological activity in this series of analogs. 3D contour maps as a result of 3D-QSAR were utilized to identify some novel features that can be incorporated into the 1,4-dihydropyridine framework to enhance the activity. (C) 2014 Elsevier Masson SAS. All rights reserved.