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6-Cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-6,9-dihydro-1H-pyrrolo[2,3-f]quinoline-2,8-dicarboxylic acid 2-benzyl ester 8-ethyl ester | 186749-27-9

中文名称
——
中文别名
——
英文名称
6-Cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-6,9-dihydro-1H-pyrrolo[2,3-f]quinoline-2,8-dicarboxylic acid 2-benzyl ester 8-ethyl ester
英文别名
2-O-benzyl 8-O-ethyl 6-cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-1H-pyrrolo[2,3-f]quinoline-2,8-dicarboxylate
6-Cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-6,9-dihydro-1H-pyrrolo[2,3-f]quinoline-2,8-dicarboxylic acid 2-benzyl ester 8-ethyl ester化学式
CAS
186749-27-9
化学式
C25H20F2N2O6
mdl
——
分子量
482.44
InChiKey
WCYVTTAXJPOEKC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    4.9
  • 重原子数:
    35
  • 可旋转键数:
    8
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    109
  • 氢给体数:
    2
  • 氢受体数:
    9

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    6-Cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-6,9-dihydro-1H-pyrrolo[2,3-f]quinoline-2,8-dicarboxylic acid 2-benzyl ester 8-ethyl ester硫酸 作用下, 以 溶剂黄146 为溶剂, 反应 2.0h, 以97%的产率得到6-Cyclopropyl-4,5-difluoro-3-hydroxy-9-oxo-6,9-dihydro-1H-pyrrolo[2,3-f]quinoline-2,8-dicarboxylic acid 2-benzyl ester
    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:
    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
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