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(S)-N-benzoyl-2,5-dimethyl-6-fluoro-1,2,3,4-tetrahydroquinoline | 107224-25-9

中文名称
——
中文别名
——
英文名称
(S)-N-benzoyl-2,5-dimethyl-6-fluoro-1,2,3,4-tetrahydroquinoline
英文别名
[(2S)-6-fluoro-2,5-dimethyl-3,4-dihydro-2H-quinolin-1-yl]-phenylmethanone
(S)-N-benzoyl-2,5-dimethyl-6-fluoro-1,2,3,4-tetrahydroquinoline化学式
CAS
107224-25-9
化学式
C18H18FNO
mdl
——
分子量
283.345
InChiKey
WABZQFUQYLZMEC-LBPRGKRZSA-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

物化性质

  • 熔点:
    99-100 °C(Solv: hexane (110-54-3))
  • 沸点:
    440.6±45.0 °C(Predicted)
  • 密度:
    1.157±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    20.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为产物:
    参考文献:
    名称:
    Synthesis, absolute configuration, and antibacterial activity of 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H-benzo[ij]quinolizine-2-carboxylic acid
    摘要:
    The tricyclic quinolone antibacterial agent 6,7-dihydro-5,8-dimethyl-9-fluoro-1-oxo-1H,5H-benzo[ij]quinolizine -2-carboxylic acid has an asymmetric center at position 5 of the molecule. The R and S isomers of the compound have been prepared from the corresponding (R)- and (S)-2,5-dimethyl-6-fluoro-1,2,3,4-tetrahydroquinolines, which were separated via their diastereomeric amides of N-tosyl-(S)-proline. The absolute configuration was established by X-ray analysis of one of the diastereomeric amides. The 5-desmethyl analogue was prepared for antibacterial comparison with the isomers and the racemic mixture. It has now been established that the S isomer is much more active than the R isomer. The 5-desmethyl analogue was found to be more active than the R isomer but not as active as the S isomer or the racemic mixture. The importance of stereochemistry at position 5 in this system has been established.
    DOI:
    10.1021/jm00388a016
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文献信息

  • GERSTER J. F.; ROHLFING S. R.; PECORE S. E.; WINANDY R. M.; STERN R. M.; +, J. MED. CHEM., 30,(1987) N 5, 839-843
    作者:GERSTER J. F.、 ROHLFING S. R.、 PECORE S. E.、 WINANDY R. M.、 STERN R. M.、 +
    DOI:——
    日期:——
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