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1-methyl-2'-O-tosylpseudouridine | 127517-32-2

中文名称
——
中文别名
——
英文名称
1-methyl-2'-O-tosylpseudouridine
英文别名
[(2S,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-2-(1-methyl-2,4-dioxopyrimidin-5-yl)oxolan-3-yl] 4-methylbenzenesulfonate
1-methyl-2'-O-tosylpseudouridine化学式
CAS
127517-32-2
化学式
C17H20N2O8S
mdl
——
分子量
412.42
InChiKey
BPGKUIFAEQJJGN-APIJFGDWSA-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):
    -0.6
  • 重原子数:
    28
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.41
  • 拓扑面积:
    151
  • 氢给体数:
    3
  • 氢受体数:
    8

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:
    3',5'-O-(1,1,3,3-tetraisopropyldisiloxan-1,3-ylene)-2'-O-tosyl-1-methylpseudouridinetriethylamine tris(hydrogen fluoride) 作用下, 以 四氢呋喃 为溶剂, 以62%的产率得到1-methyl-2'-O-tosylpseudouridine
    参考文献:
    名称:
    Nucleosides. 153. Synthesis of 1-methyl-5-(3-azido-2,3-dideoxy-.beta.-D-erythro-pentofuranosyl)uracil and 1-methyl-5-(3-azido-2,3-dideoxy-2-fluoro-.beta.-D-arabinofuranosyl)uracil. The C-nucleoside isostere of 3'-azido-3'-deoxythymidine and its 2'-"up"-fluoro analog
    摘要:
    1-Methyl-5-(3-azido-2,3-dideoxy-beta-D-erythro-pentofuranosyl)uracil (C-AZT), a C-nucleoside isostere of the potent anti-AIDS nucleoside 3'-azido-3'-deoxythymidine (AZT), was synthesized. 1-Methyl-2'-deoxy-5'-O-tritylpseudouridine (2a) was oxidized with CrO3/pyridine/Ac2O complex to 1-methyl-5-(5-O-trityl-beta-D-glycero-pentofuranos-3-ulosyl) uracil (12a), which was selectively reduced to 1-methyl-5-(5-O-trityl-beta-D-threo-pentofuranosyl)uracil (13a). Mesylation of 13a to 14a followed by nucleophilic displacement of the mesyloxy group with azide afforded 3'-azido-2',3'-dideoxy-5'-O-trityl-1-methylpseudoridine (15a), which was detritylated to C-AZT. In a similar manner, 1-methyl-5-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil (C-FMAU, a potent antiherpetic nucleoside) was converted into the 3'-azido analogue (3'-azido-C-FMAU). Both C-AZT and 3'-azido-C-FMAU, however, did not exhibit any significant inhibitory activity against HIV in H9 cells.
    DOI:
    10.1021/jm00169a030
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文献信息

  • SOCHACKA, ELZBIETA;NAWROT, BARBARA;PANKIEWICZ, KRZYSZTOF W.;WATANABE, KYO+, J. MED. CHEM., 33,(1990) N, C. 1995-1999
    作者:SOCHACKA, ELZBIETA、NAWROT, BARBARA、PANKIEWICZ, KRZYSZTOF W.、WATANABE, KYO+
    DOI:——
    日期:——
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