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ethyl 8-fluoro-4-methyl-1-oxo-7-[4-(3-trifluoromethylphenyl)piperazin-1-yl]-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylate | 318685-14-2

中文名称
——
中文别名
——
英文名称
ethyl 8-fluoro-4-methyl-1-oxo-7-[4-(3-trifluoromethylphenyl)piperazin-1-yl]-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylate
英文别名
Ethyl 8-fluoro-4-methyl-1-oxo-7-[4-[3-(trifluoromethyl)phenyl]piperazin-1-yl]benzo[f][1,7]naphthyridine-2-carboxylate
ethyl 8-fluoro-4-methyl-1-oxo-7-[4-(3-trifluoromethylphenyl)piperazin-1-yl]-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylate化学式
CAS
318685-14-2
化学式
C27H24F4N4O3
mdl
——
分子量
528.506
InChiKey
AQWYIORQVZNMQX-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):
    5.1
  • 重原子数:
    38
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    66
  • 氢给体数:
    0
  • 氢受体数:
    11

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:
    ethyl 8-fluoro-4-methyl-1-oxo-7-[4-(3-trifluoromethylphenyl)piperazin-1-yl]-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylate氢氧化钾 作用下, 以 乙醇 为溶剂, 生成 8-fluoro-4-methyl-1-oxo-7-[4-(3-trifluoromethylphenyl)piperazin-1-yl]-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylic acid
    参考文献:
    名称:
    Benzo[f]naphtyridones: a new family of topical antibacterial agents active on multi-resistant Gram-positive pathogens
    摘要:
    The synthesis and antibacterial activity of benzo[f][1,7]naphtyridone derivatives are reported. These compounds are potent antibacterial agents with a Gram-positive spectrum of activity. They are active against multi-resistant cocci, especially Staphylococcus aureus strains. Their physico-chemical and biological properties make them particularly suitable for topical antibacterial use. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00057-x
  • 作为产物:
    描述:
    1-(3-三氟甲基苯基)哌嗪ethyl 7,8-difluoro-4-methyl-1-oxo-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylate二甲基亚砜 为溶剂, 生成 ethyl 8-fluoro-4-methyl-1-oxo-7-[4-(3-trifluoromethylphenyl)piperazin-1-yl]-1,4-dihydrobenzo[f] [1,7]naphthyridine-2-carboxylate 、 7-Fluoro-4-methyl-1-oxo-8-[4-(3-trifluoromethyl-phenyl)-piperazin-1-yl]-1,4-dihydro-benzo[f][1,7]naphthyridine-2-carboxylic acid ethyl ester
    参考文献:
    名称:
    Benzo[f]naphtyridones: a new family of topical antibacterial agents active on multi-resistant Gram-positive pathogens
    摘要:
    The synthesis and antibacterial activity of benzo[f][1,7]naphtyridone derivatives are reported. These compounds are potent antibacterial agents with a Gram-positive spectrum of activity. They are active against multi-resistant cocci, especially Staphylococcus aureus strains. Their physico-chemical and biological properties make them particularly suitable for topical antibacterial use. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(03)00057-x
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文献信息

  • Benzo[f]naphthyridine derivatives, their preparation and compositions containing them
    申请人:——
    公开号:US20020137741A1
    公开(公告)日:2002-09-26
    Benzo[f]naphthyridine derivatives of formula (I): 1 benzo[f]naphthyridine derivatives and benzo[f]naphthyridine esters of formula (IVa): 2 aminoquinoline derivatives of formula (X): 3 processes for preparing such compounds; and compositions comprising them.
    苯并[f]啉衍生物化学式(I):1苯并[f]啉衍生物和苯并[f]啉酯的化学式(IVa);2喹啉生物化学式(X);3制备这些化合物的方法;以及包含它们的组合物。
  • US6566362B2
    申请人:——
    公开号:US6566362B2
    公开(公告)日:2003-05-20
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