Diethyl 5-(cyanomethylamino)-1-cyclopropyl-7,8-difluoro-4-oxoquinoline-3,6-dicarboxylate | 186749-26-8

• 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: Diethyl 5-(cyanomethylamino)-1-cyclopropyl-7,8-difluoro-4-oxoquinoline-3,6-dicarboxylate
• CAS: 186749-26-8
• 化学式: C₂₀H₁₉F₂N₃O₅
• 分子量: 419.385
• InChiKey: UCKJZRUEQWGACY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  30
• 可旋转键数：
  9
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.4
• 拓扑面积：
  109
• 氢给体数：
  1
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  Diethyl 5-(cyanomethylamino)-1-cyclopropyl-7,8-difluoro-4-oxoquinoline-3,6-dicarboxylate 在 硫酸 、 potassium tert-butylate 作用下， 以 四氢呋喃 、 溶剂黄146 、 叔丁醇 为溶剂， 反应 2.33h， 生成 2-Cyano-6-cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-6,9-dihydro-1H-pyrrolo[2,3-f]quinoline-8-carboxylic acid
  参考文献：
  名称：

  Pyrroloquinolones and pyrazoloquinolones as potential antibacterial agents. Synthesis and antibacterial activity

  摘要：

  Diethyl 1-cyclopropyl-5,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3,6-dicarboxylate as a key-intermediate was synthesized via the Dieckmann reaction. The reaction of 4 with nucleophiles proceeded regioselectively at C-5. Facile cyclization between the C-5 and C-6 side chains of the resulting products gave novel pyrroloquinolones 10 and 12 and pyrazoloquinolones 15. They were converted into a series of cyclic amino-substituted pyrroloquinolones 17-21 and pyrazoloquinolones 22-24, and their in vitro antibacterial activities were tested. 1H-Pyrrolo[2,3-f]quinolone 17a and 2H-pyrrolo[3,4-f]quinolone 21a exhibited a potent in vitro antibacterial activity.

  DOI：

  10.1016/s0223-5234(97)86177-6
• 作为产物：
  描述：

  ethyl 3-cyclopropylaminopropionate 在 potassium tert-butylate 、 溴 、 碳酸氢钠 、 potassium carbonate 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 、 叔丁醇 为溶剂， 反应 9.5h， 生成 Diethyl 5-(cyanomethylamino)-1-cyclopropyl-7,8-difluoro-4-oxoquinoline-3,6-dicarboxylate
  参考文献：
  名称：

  Pyrroloquinolones and pyrazoloquinolones as potential antibacterial agents. Synthesis and antibacterial activity

  摘要：

  Diethyl 1-cyclopropyl-5,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3,6-dicarboxylate as a key-intermediate was synthesized via the Dieckmann reaction. The reaction of 4 with nucleophiles proceeded regioselectively at C-5. Facile cyclization between the C-5 and C-6 side chains of the resulting products gave novel pyrroloquinolones 10 and 12 and pyrazoloquinolones 15. They were converted into a series of cyclic amino-substituted pyrroloquinolones 17-21 and pyrazoloquinolones 22-24, and their in vitro antibacterial activities were tested. 1H-Pyrrolo[2,3-f]quinolone 17a and 2H-pyrrolo[3,4-f]quinolone 21a exhibited a potent in vitro antibacterial activity.

  DOI：

  10.1016/s0223-5234(97)86177-6

文献信息

• Pyrroloquinolones and pyrazoloquinolones as potential antibacterial agents. Synthesis and antibacterial activity
  作者：M Fujita、H Egawa、T Miyamoto、J Nakano、J Matsumoto

  DOI：10.1016/s0223-5234(97)86177-6

  日期：1996.1

  Diethyl 1-cyclopropyl-5,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3,6-dicarboxylate as a key-intermediate was synthesized via the Dieckmann reaction. The reaction of 4 with nucleophiles proceeded regioselectively at C-5. Facile cyclization between the C-5 and C-6 side chains of the resulting products gave novel pyrroloquinolones 10 and 12 and pyrazoloquinolones 15. They were converted into a series of cyclic amino-substituted pyrroloquinolones 17-21 and pyrazoloquinolones 22-24, and their in vitro antibacterial activities were tested. 1H-Pyrrolo[2,3-f]quinolone 17a and 2H-pyrrolo[3,4-f]quinolone 21a exhibited a potent in vitro antibacterial activity.