N-[2-(4-methoxyphenyl)-4-oxo-1,3-thiazolidin-3-yl]-2-(5-nitroindazol-1-yl)acetamide | 1245567-35-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡唑类
• 英文名称: N-[2-(4-methoxyphenyl)-4-oxo-1,3-thiazolidin-3-yl]-2-(5-nitroindazol-1-yl)acetamide
• CAS: 1245567-35-4
• 化学式: C₁₉H₁₇N₅O₅S
• 分子量: 427.44
• InChiKey: ZFBMCYCIMNCHEE-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.6
• 重原子数：
  30
• 可旋转键数：
  4
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  148
• 氢给体数：
  1
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  N-(N-(4-methoxybenzylideneamino)acetamidyl)-5-nitroindazole 、 巯基乙酸 在 zinc(II) chloride 作用下， 反应 0.07h， 以91%的产率得到N-[2-(4-methoxyphenyl)-4-oxo-1,3-thiazolidin-3-yl]-2-(5-nitroindazol-1-yl)acetamide
  参考文献：
  名称：

  Conventional and microwave assisted synthesis of Some new N-[(4-oxo-2-substituted aryl −1, 3-thiazolidine)-acetamidyl]-5-nitroindazoles and its antimicrobial activity

  摘要：

  Several new N-[(4-oxo-2-substituted aryl-1, 3-thiazolidine)-acetamidyl]-5-nitroindazoles (4a-1) were synthesized from N-(arylidene amino acetamidyl)-5-nitroindazoles (3a-1). The reactions were carried out by both conventional as well as microwave method. The structures of these compounds were confirmed by IR, H-1 NMR, C-13 NMR, FAB-mass spectra and also by microanalytical data. The newly synthesized compounds were evaluated for their antimicrobial activity against variety of bacterial and fungal strains. The compounds 4g and 4h showed the maximum antibacterial activity (MIC 11 and 10 mu g/mL) against Escherichia coli and antifungal activity (MIC 9 and 8 mu g/mL) against Fusarium oxysporum. (C) 2010 Elsevier Masson SAS. All rights reserved.

  DOI：

  10.1016/j.ejmech.2010.04.029

文献信息

• Conventional and microwave assisted synthesis of Some new N-[(4-oxo-2-substituted aryl −1, 3-thiazolidine)-acetamidyl]-5-nitroindazoles and its antimicrobial activity
  作者：Apoorva Upadhyay、S.K. Srivastava、S.D. Srivastava

  DOI：10.1016/j.ejmech.2010.04.029

  日期：2010.9

  Several new N-[(4-oxo-2-substituted aryl-1, 3-thiazolidine)-acetamidyl]-5-nitroindazoles (4a-1) were synthesized from N-(arylidene amino acetamidyl)-5-nitroindazoles (3a-1). The reactions were carried out by both conventional as well as microwave method. The structures of these compounds were confirmed by IR, H-1 NMR, C-13 NMR, FAB-mass spectra and also by microanalytical data. The newly synthesized compounds were evaluated for their antimicrobial activity against variety of bacterial and fungal strains. The compounds 4g and 4h showed the maximum antibacterial activity (MIC 11 and 10 mu g/mL) against Escherichia coli and antifungal activity (MIC 9 and 8 mu g/mL) against Fusarium oxysporum. (C) 2010 Elsevier Masson SAS. All rights reserved.