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4-(benzoyl)-1-(5-deoxy-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)-5-(3-nitrophenyl)-1H-1,2,3-triazole | 1242261-29-5

中文名称
——
中文别名
——
英文名称
4-(benzoyl)-1-(5-deoxy-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)-5-(3-nitrophenyl)-1H-1,2,3-triazole
英文别名
[1-[[(3aR,5R,6S,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]methyl]-5-(3-nitrophenyl)triazol-4-yl]-phenylmethanone
4-(benzoyl)-1-(5-deoxy-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)-5-(3-nitrophenyl)-1H-1,2,3-triazole化学式
CAS
1242261-29-5
化学式
C23H22N4O7
mdl
——
分子量
466.45
InChiKey
PVHVOSKUCJHYBQ-IDZYALCFSA-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):
    2.3
  • 重原子数:
    34
  • 可旋转键数:
    5
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    142
  • 氢给体数:
    1
  • 氢受体数:
    9

反应信息

  • 作为产物:
    描述:
    5-azido-5-deoxy-1,2-O-isopropylidene-α-D-xylofuranose(E)-3-nitrochalcone 在 tetrabutylammonium hydrogen sulfate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 24.0h, 以83%的产率得到4-(benzoyl)-1-(5-deoxy-1,2-O-isopropylidene-α-D-xylofuranos-5-yl)-5-(3-nitrophenyl)-1H-1,2,3-triazole
    参考文献:
    名称:
    Regioselective [3+2] cycloaddition of chalcones with a sugar azide: easy access to 1-(5-deoxy-d-xylofuranos-5-yl)-4,5-disubstituted-1H-1,2,3-triazoles
    摘要:
    [3+2] Cycloaddition of 5-azido-5-deoxy-1,2-O-isopropylidene-alpha-D-xylofuranose with 1,3-diphenylprop-3-enones, followed by oxidation of the intermediate triazolines in a tandem manner, led to the regioselective formation of 4-benzoyl-1-(5-deoxy-1,2-O-isopropylidene-alpha-D-xylofuranos-5-yl)-5-phenyl-1H-1,2,3-triazoles in moderate to good yields. (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.carres.2010.04.019
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文献信息

  • Regioselective [3+2] cycloaddition of chalcones with a sugar azide: easy access to 1-(5-deoxy-d-xylofuranos-5-yl)-4,5-disubstituted-1H-1,2,3-triazoles
    作者:Nimisha Singh、S.K. Pandey、Rama P. Tripathi
    DOI:10.1016/j.carres.2010.04.019
    日期:2010.8
    [3+2] Cycloaddition of 5-azido-5-deoxy-1,2-O-isopropylidene-alpha-D-xylofuranose with 1,3-diphenylprop-3-enones, followed by oxidation of the intermediate triazolines in a tandem manner, led to the regioselective formation of 4-benzoyl-1-(5-deoxy-1,2-O-isopropylidene-alpha-D-xylofuranos-5-yl)-5-phenyl-1H-1,2,3-triazoles in moderate to good yields. (C) 2010 Elsevier Ltd. All rights reserved.
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