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7-Chloro-1-cyclopropyl-8-ethyl-6-nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid | 258346-01-9

中文名称
——
中文别名
——
英文名称
7-Chloro-1-cyclopropyl-8-ethyl-6-nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
英文别名
——
7-Chloro-1-cyclopropyl-8-ethyl-6-nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid化学式
CAS
258346-01-9
化学式
C15H13ClN2O5
mdl
——
分子量
336.732
InChiKey
YYAYQSOAUHOCOQ-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):
    3.16
  • 重原子数:
    23.0
  • 可旋转键数:
    4.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    102.44
  • 氢给体数:
    1.0
  • 氢受体数:
    5.0

反应信息

  • 作为反应物:
    描述:
    7-Chloro-1-cyclopropyl-8-ethyl-6-nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid 氢气三乙胺 作用下, 以 乙醇N,N-二甲基甲酰胺乙腈 为溶剂, 20.0 ℃ 、207.72 kPa 条件下, 反应 36.0h, 生成 6-Amino-1-cyclopropyl-7-(3,4-dihydro-1H-isoquinolin-2-yl)-8-ethyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
    参考文献:
    名称:
    Studies on 6-Aminoquinolones: synthesis and antibacterial evaluation of 6-amino-8-ethyl- and 6-amino-8-methoxyquinolones
    摘要:
    From our quantitative structure-activity relationship (QSAR) study on a large set of 6-aminoquinolones, which indicated that a group larger than methyl could be allocated at C-8 position, we have synthesized two new series of 6-aminoquinolones characterized by the presence of an ethyl or a methoxy group at C-8 position. The antibacterial evaluation shows that, while the 8-ethyl derivatives were devoid of any antibacterial activity, the introduction of methoxy group gave compounds with good antibacterial activity, especially against Gram-positive bacteria. A tentative explanation of the different behaviours among the 8-substituted analogues is given taking into account both the length and electronic properties of the C-8 groups. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(99)00207-2
  • 作为产物:
    描述:
    ethyl 1-cyclopropyl-6-chloro-8-ethyl-6-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylate盐酸 作用下, 以 乙醇 为溶剂, 反应 3.0h, 以93%的产率得到7-Chloro-1-cyclopropyl-8-ethyl-6-nitro-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid
    参考文献:
    名称:
    Studies on 6-Aminoquinolones: synthesis and antibacterial evaluation of 6-amino-8-ethyl- and 6-amino-8-methoxyquinolones
    摘要:
    From our quantitative structure-activity relationship (QSAR) study on a large set of 6-aminoquinolones, which indicated that a group larger than methyl could be allocated at C-8 position, we have synthesized two new series of 6-aminoquinolones characterized by the presence of an ethyl or a methoxy group at C-8 position. The antibacterial evaluation shows that, while the 8-ethyl derivatives were devoid of any antibacterial activity, the introduction of methoxy group gave compounds with good antibacterial activity, especially against Gram-positive bacteria. A tentative explanation of the different behaviours among the 8-substituted analogues is given taking into account both the length and electronic properties of the C-8 groups. (C) 1999 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(99)00207-2
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