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N-[9-[(2R,3R,4R,5R)-4-[tert-butyl(diphenyl)silyl]oxy-3-methoxy-5-[(methylideneamino)oxymethyl]oxolan-2-yl]purin-6-yl]benzamide | 199581-55-0

中文名称
——
中文别名
——
英文名称
N-[9-[(2R,3R,4R,5R)-4-[tert-butyl(diphenyl)silyl]oxy-3-methoxy-5-[(methylideneamino)oxymethyl]oxolan-2-yl]purin-6-yl]benzamide
英文别名
——
N-[9-[(2R,3R,4R,5R)-4-[tert-butyl(diphenyl)silyl]oxy-3-methoxy-5-[(methylideneamino)oxymethyl]oxolan-2-yl]purin-6-yl]benzamide化学式
CAS
199581-55-0
化学式
C35H38N6O5Si
mdl
——
分子量
650.809
InChiKey
MCCBNMBGTLZLCV-WIFIACMTSA-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):
    4.57
  • 重原子数:
    47
  • 可旋转键数:
    12
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    122
  • 氢给体数:
    1
  • 氢受体数:
    9

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

  • 作为反应物:
    描述:
    N-[9-[(2R,3R,4R,5R)-4-[tert-butyl(diphenyl)silyl]oxy-3-methoxy-5-[(methylideneamino)oxymethyl]oxolan-2-yl]purin-6-yl]benzamide盐酸 、 sodium cyanoborohydride 作用下, 以 甲醇 为溶剂, 生成 N-(9-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-9H-purin-6-yl)-benzamide
    参考文献:
    名称:
    An Efficient Multigram Synthesis of Monomers for the Preparation of Novel Oligonucleotides Containing Isosteric Non-Phosphorous Backbones
    摘要:
    The facile preparation of two novel classes of nucleoside analogs for the inclusion as dimeric non-phosphorous containing subunits in chimeric backbones has been accomplished. The concise preparation of 3'-formylnucleosides and 5'-O-(N-methylhydroxylamino)-nucleosides is reported.
    DOI:
    10.1080/07328319708006242
  • 作为产物:
    参考文献:
    名称:
    An Efficient Multigram Synthesis of Monomers for the Preparation of Novel Oligonucleotides Containing Isosteric Non-Phosphorous Backbones
    摘要:
    The facile preparation of two novel classes of nucleoside analogs for the inclusion as dimeric non-phosphorous containing subunits in chimeric backbones has been accomplished. The concise preparation of 3'-formylnucleosides and 5'-O-(N-methylhydroxylamino)-nucleosides is reported.
    DOI:
    10.1080/07328319708006242
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文献信息

  • A mild and highly selective N-benzoylation of cytosine and adenine bases in nucleosides with N-benzoyltetrazole
    作者:Balkrishen Bhat、Yogesh S. Sanghvi
    DOI:10.1016/s0040-4039(97)10423-3
    日期:1997.12
    N-Benzoyltetrazole has been developed as a mild and selective reagent for monobenzoylation of the exocyclic amino group in nucleic acid bases. its usefulness is demonstrated by protection of adenine and cytosine bases, an important procedure in the nucleic acid chemistry field. (C) 1997 Elsevier Science Ltd.
  • An Efficient Multigram Synthesis of Monomers for the Preparation of Novel Oligonucleotides Containing Isosteric Non-Phosphorous Backbones
    作者:Stuart Dimock、Balkrishen Bhat、Didier Peoc'h、Yogesh S. Sanghvi、Eric E. Swayze
    DOI:10.1080/07328319708006242
    日期:1997.7
    The facile preparation of two novel classes of nucleoside analogs for the inclusion as dimeric non-phosphorous containing subunits in chimeric backbones has been accomplished. The concise preparation of 3'-formylnucleosides and 5'-O-(N-methylhydroxylamino)-nucleosides is reported.
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