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2-(N-tert-butylhydroxylamino)-2'-deoxyinosine | 844877-68-5

中文名称
——
中文别名
——
英文名称
2-(N-tert-butylhydroxylamino)-2'-deoxyinosine
英文别名
2-[tert-butyl(hydroxy)amino]-9-[(2R,4S,5R)-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-1H-purin-6-one
2-(N-tert-butylhydroxylamino)-2'-deoxyinosine化学式
CAS
844877-68-5
化学式
C14H21N5O5
mdl
——
分子量
339.351
InChiKey
KXGQTZUFYRHURA-DJLDLDEBSA-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):
    -0.2
  • 重原子数:
    24
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    132
  • 氢给体数:
    4
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    2-(N-tert-butylhydroxylamino)-2'-deoxyinosinesodium periodate 作用下, 以 为溶剂, 反应 0.17h, 以95%的产率得到2-N-tert-butylaminoxyl-2'-deoxyinosine
    参考文献:
    名称:
    Synthesis and EPR Studies of 2-N-tert-Butylaminoxylpurine Derivatives
    摘要:
    2'-Deoxyribofuranosylpurine derivatives bearing an N-tert-butylaminoxyl group (1a and 2a) were synthesized via oxidation of the corresponding N-tert-butylhydroxylamines (1b and 2b), which were synthesized by lithiation of 8-TIPS-6-chloropurine (3) at the 2-position and the following reaction with 2-methyl-2-nitrosopropane. Treatment of 1b and 2b with 1 equiv of NalO(4) resulted in efficient formation of la and 2a. which were isolated as purple and red solids, respectively. The EPR spectra of la showed pH dependency due to structural change of purine moiety.
    DOI:
    10.1021/ol047668t
  • 作为产物:
    描述:
    [[9-[(6aR,8R,9aS)-2,2,4,4-tetra(propan-2-yl)-6a,8,9,9a-tetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl]-6-oxo-1H-purin-2-yl]-tert-butylamino] acetate 在 氟化铵 作用下, 以 甲醇 为溶剂, 反应 4.0h, 以77%的产率得到2-(N-tert-butylhydroxylamino)-2'-deoxyinosine
    参考文献:
    名称:
    Synthesis and EPR Studies of 2-N-tert-Butylaminoxylpurine Derivatives
    摘要:
    2'-Deoxyribofuranosylpurine derivatives bearing an N-tert-butylaminoxyl group (1a and 2a) were synthesized via oxidation of the corresponding N-tert-butylhydroxylamines (1b and 2b), which were synthesized by lithiation of 8-TIPS-6-chloropurine (3) at the 2-position and the following reaction with 2-methyl-2-nitrosopropane. Treatment of 1b and 2b with 1 equiv of NalO(4) resulted in efficient formation of la and 2a. which were isolated as purple and red solids, respectively. The EPR spectra of la showed pH dependency due to structural change of purine moiety.
    DOI:
    10.1021/ol047668t
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