1-cyclopropyl-6-fluoro-4-oxo-7-(4-phenylaminomethyl-[1,2,3]triazol-1-yl)-1,4-dihydro-quinoline-3-carboxylic acid | 1416988-30-1

• 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-cyclopropyl-6-fluoro-4-oxo-7-(4-phenylaminomethyl-[1,2,3]triazol-1-yl)-1,4-dihydro-quinoline-3-carboxylic acid
• 英文别名: 7-[4-(Anilinomethyl)triazol-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid；7-[4-(anilinomethyl)triazol-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid
• CAS: 1416988-30-1
• 化学式: C₂₂H₁₈FN₅O₃
• 分子量: 419.415
• InChiKey: VYMRFWDUIIYMKX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  31
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.18
• 拓扑面积：
  100
• 氢给体数：
  2
• 氢受体数：
  8

反应信息

• 作为产物：
  描述：

  1-环丙基-6,7-二氟-4-氧代-1,4-二氢喹啉-3-羧酸乙酯 在 吡啶 、 盐酸 、 copper(l) iodide 、 氯化亚砜 、 sodium azide 、 sodium ascorbate 、 三乙胺 、 N,N-二异丙基乙胺 、 potassium iodide 作用下， 以 二氯甲烷 、 水 、 N,N-二甲基甲酰胺 为溶剂， 反应 32.34h， 生成 1-cyclopropyl-6-fluoro-4-oxo-7-(4-phenylaminomethyl-[1,2,3]triazol-1-yl)-1,4-dihydro-quinoline-3-carboxylic acid
  参考文献：
  名称：

  Design and synthesis of new N-substituted amino methyl-[1,2,3] triazolyl moieties of fluoroquinolones as antibacterial agents

  摘要：

  A series of twenty new N-substituted amino methyl-[1,2,3] triazolyl derivatives at C-7 position of fluoroquinolones were designed and synthesized through multistep synthesis. The synthesized compounds were characterized by H-1 NMR, C-13 NMR, ESI-MS, and IR. The antibacterial activities of these new fluoroquinolones were evaluated using a standard broth micro dilution technique. Out of the twenty derivatives, aryl substituted amino derivatives (6m to 6q) exhibited very good potency in inhibiting the growth of Methicillin-sensitive Staphylococcus aureus (MSSA), Methicillin-resistant Staphylococcus aureus (MRSA), and Vancomycin-Resistant Enterococcus faecalis (VRE faecalis) (MIC: 0.25-4.00 mu g/mL) as compared to the marketed drugs Linezolid and Ciprofloxacin.

  DOI：

  10.1007/s00044-012-0394-2

文献信息

• Design and synthesis of new N-substituted amino methyl-[1,2,3] triazolyl moieties of fluoroquinolones as antibacterial agents
  作者：G. Govinda Rajulu、Halehatty S. Bhojya Naik、Abhilash Viswanathan、Devesh S. Agarwal、Ganesh Sambasivam、Kesavan Poonimangadu Koppolu

  DOI：10.1007/s00044-012-0394-2

  日期：2013.8

  A series of twenty new N-substituted amino methyl-[1,2,3] triazolyl derivatives at C-7 position of fluoroquinolones were designed and synthesized through multistep synthesis. The synthesized compounds were characterized by H-1 NMR, C-13 NMR, ESI-MS, and IR. The antibacterial activities of these new fluoroquinolones were evaluated using a standard broth micro dilution technique. Out of the twenty derivatives, aryl substituted amino derivatives (6m to 6q) exhibited very good potency in inhibiting the growth of Methicillin-sensitive Staphylococcus aureus (MSSA), Methicillin-resistant Staphylococcus aureus (MRSA), and Vancomycin-Resistant Enterococcus faecalis (VRE faecalis) (MIC: 0.25-4.00 mu g/mL) as compared to the marketed drugs Linezolid and Ciprofloxacin.