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methyl 4-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methylamino)-6-methyl-2-oxocyclohex-3-enecarboxylate | 1147846-91-0

中文名称
——
中文别名
——
英文名称
methyl 4-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methylamino)-6-methyl-2-oxocyclohex-3-enecarboxylate
英文别名
methyl 4-[[(5S)-3-(3-fluoro-4-morpholin-4-ylphenyl)-2-oxo-1,3-oxazolidin-5-yl]methylamino]-6-methyl-2-oxocyclohex-3-ene-1-carboxylate
methyl 4-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methylamino)-6-methyl-2-oxocyclohex-3-enecarboxylate化学式
CAS
1147846-91-0
化学式
C23H28FN3O6
mdl
——
分子量
461.49
InChiKey
WFBKWLBQBQAQHP-XZSJUEPFSA-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:
    207-209 °C(Solvent: Ethanol)
  • 沸点:
    636.7±55.0 °C(predicted)
  • 密度:
    1.35±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    33
  • 可旋转键数:
    7
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.52
  • 拓扑面积:
    97.4
  • 氢给体数:
    1
  • 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

  • 作为产物:
    描述:
    methyl 2-hydroxy-6-methyl-4-oxocyclohex-2-ene-1-carboxylate利奈唑胺碱 以77%的产率得到methyl 4-(((S)-3-(3-fluoro-4-morpholinophenyl)-2-oxooxazolidin-5-yl)methylamino)-6-methyl-2-oxocyclohex-3-enecarboxylate
    参考文献:
    名称:
    Synthesis, antibacterial and anticonvulsant evaluations of some cyclic enaminones
    摘要:
    Several cyclic enaminone esters were synthesized, characterized, and evaluated for anticonvulsant and antibacterial activities using standardized tests, A series of enaminones were mainly phenyl analogs of anticonvulsant enaminones, while a second series comprised of compounds bearing the oxazolidinone pharmacophoric moiety found in the synthetic antibacterial linezolid. The enaminone ester bearing an unsubstituted anilino analog showed class 2 anticonvulsant activity. This represents a first report of an unsubstituted anilino enaminone with anticonvulsant activity. The enaminone esters gave interesting UV data, and four analogs displayed potent anticonvulsant activities, while another four compounds showed moderate anticonvulsant activities. Surprisingly, none of the enaminone esters had any significant antibacterial activity. (C) 2008 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2008.07.005
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文献信息

  • Synthesis, antibacterial and anticonvulsant evaluations of some cyclic enaminones
    作者:Ivan O. Edafiogho、Oludotun A. Phillips、Edet E. Udo、Santosh Samuel、Beigy Rethish
    DOI:10.1016/j.ejmech.2008.07.005
    日期:2009.3
    Several cyclic enaminone esters were synthesized, characterized, and evaluated for anticonvulsant and antibacterial activities using standardized tests, A series of enaminones were mainly phenyl analogs of anticonvulsant enaminones, while a second series comprised of compounds bearing the oxazolidinone pharmacophoric moiety found in the synthetic antibacterial linezolid. The enaminone ester bearing an unsubstituted anilino analog showed class 2 anticonvulsant activity. This represents a first report of an unsubstituted anilino enaminone with anticonvulsant activity. The enaminone esters gave interesting UV data, and four analogs displayed potent anticonvulsant activities, while another four compounds showed moderate anticonvulsant activities. Surprisingly, none of the enaminone esters had any significant antibacterial activity. (C) 2008 Elsevier Masson SAS. All rights reserved.
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