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(R)-6,8-dibromo-5-(2,3-epoxyprop-1-yloxy)-quinoline | 188594-92-5

中文名称
——
中文别名
——
英文名称
(R)-6,8-dibromo-5-(2,3-epoxyprop-1-yloxy)-quinoline
英文别名
6,8-dibromo-5-[[(2R)-oxiran-2-yl]methoxy]quinoline
(R)-6,8-dibromo-5-(2,3-epoxyprop-1-yloxy)-quinoline化学式
CAS
188594-92-5
化学式
C12H9Br2NO2
mdl
——
分子量
359.017
InChiKey
SAFOEPXFXOQIKN-SSDOTTSWSA-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):
    3.2
  • 重原子数:
    17
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    34.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    (R)-6,8-dibromo-5-(2,3-epoxyprop-1-yloxy)-quinoline 在 10% palladium on active carbon 氢氧化钾超重氢 作用下, 以 甲醇乙酸乙酯异丙醇 为溶剂, 反应 8.0h, 生成 1-[4-(trans-11,11-difluorodibenzo[b,e]bicyclo[5.1.0]oct-5-yl)-piperazin-1-yl]-3-(6,8-ditritioquinolin-5-yl)oxy-(R)-2-propanol
    参考文献:
    名称:
    Synthesis of multidrug resistance modulator LY335979 labeled with deuterium and tritium
    摘要:
    Dideutero and ditritioisotopomers of the multidrug resistance modulator LY335979 were prepared by initial bromination of 5-hydroxyquinoline under acidic conditions followed by Mitsunobu coupling of 6,8-dibromo-5-hydroxyquinoline with (S)-glycidol. Opening of the resulting epoxide with dibenzosuberylpiperazine LY335995 resulted in dibromoanalog of LY335979, which was finally reductively debrominated with deuterium or tritium in the presence of palladium on carbon.
    DOI:
    10.1002/(sici)1099-1344(199701)39:1<49::aid-jlcr938>3.0.co;2-m
  • 作为产物:
    描述:
    6,8-Dibromo-quinolin-5-ol; hydrobromide(S)-缩水甘油三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃 为溶剂, 以97%的产率得到(R)-6,8-dibromo-5-(2,3-epoxyprop-1-yloxy)-quinoline
    参考文献:
    名称:
    Synthesis of multidrug resistance modulator LY335979 labeled with deuterium and tritium
    摘要:
    Dideutero and ditritioisotopomers of the multidrug resistance modulator LY335979 were prepared by initial bromination of 5-hydroxyquinoline under acidic conditions followed by Mitsunobu coupling of 6,8-dibromo-5-hydroxyquinoline with (S)-glycidol. Opening of the resulting epoxide with dibenzosuberylpiperazine LY335995 resulted in dibromoanalog of LY335979, which was finally reductively debrominated with deuterium or tritium in the presence of palladium on carbon.
    DOI:
    10.1002/(sici)1099-1344(199701)39:1<49::aid-jlcr938>3.0.co;2-m
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