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(2R,3R,4R,5R)-2-(5-((1H-imidazol-4-yl)selanyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate | 1233477-39-8

中文名称
——
中文别名
——
英文名称
(2R,3R,4R,5R)-2-(5-((1H-imidazol-4-yl)selanyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
英文别名
——
(2R,3R,4R,5R)-2-(5-((1H-imidazol-4-yl)selanyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate化学式
CAS
1233477-39-8
化学式
C18H20N4O9Se
mdl
——
分子量
515.338
InChiKey
VIGXVFLXKLHGHB-BNGXUDDSSA-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):
    -2.76
  • 重原子数:
    32.0
  • 可旋转键数:
    7.0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    171.67
  • 氢给体数:
    2.0
  • 氢受体数:
    11.0

反应信息

  • 作为反应物:
    描述:
    (2R,3R,4R,5R)-2-(5-((1H-imidazol-4-yl)selanyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetatesodium methylate 作用下, 以 甲醇 为溶剂, 反应 0.5h, 以100%的产率得到1-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-(1H-imidazol-5-ylselanyl)pyrimidine-2,4-dione
    参考文献:
    名称:
    Electrophilic Aromatic Selenylation: New OPRT Inhibitors
    摘要:
    2-Ethoxyethaneseleninic acid reacts with electron-rich aromatic substrates to deliver, by way of the selenoxides, the (2-ethoxyethyl)seleno ethers, which can in turn be transformed into a diverse set of aryl-selenylated products. Among these, a family of 5-uridinyl derivatives shows submicromolar inhibition of human and malarial orotate phosphoribosyltransferase.
    DOI:
    10.1021/ol1010032
  • 作为产物:
    描述:
    三甲基硅咪唑二氯甲烷 为溶剂, 反应 0.5h, 以8.7 mg的产率得到(2R,3R,4R,5R)-2-(5-((1H-imidazol-4-yl)selanyl)-2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-5-(acetoxymethyl)tetrahydrofuran-3,4-diyl diacetate
    参考文献:
    名称:
    Electrophilic Aromatic Selenylation: New OPRT Inhibitors
    摘要:
    2-Ethoxyethaneseleninic acid reacts with electron-rich aromatic substrates to deliver, by way of the selenoxides, the (2-ethoxyethyl)seleno ethers, which can in turn be transformed into a diverse set of aryl-selenylated products. Among these, a family of 5-uridinyl derivatives shows submicromolar inhibition of human and malarial orotate phosphoribosyltransferase.
    DOI:
    10.1021/ol1010032
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