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2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine | 160905-77-1

中文名称
——
中文别名
——
英文名称
2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine
英文别名
N-[9-[(2R,3R,4R,5R)-3-[1-(2-fluorophenyl)-4-methoxypiperidin-4-yl]oxy-5-(hydroxymethyl)-4-(9-phenylxanthen-9-yl)oxyoxolan-2-yl]purin-6-yl]-2,2-dimethylpropanamide
2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine化学式
CAS
160905-77-1
化学式
C46H47FN6O7
mdl
——
分子量
814.914
InChiKey
CNRZKFXBVNXCJU-CISTVLBBSA-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):
    6.4
  • 重原子数:
    60
  • 可旋转键数:
    11
  • 环数:
    9.0
  • sp3杂化的碳原子比例:
    0.35
  • 拓扑面积:
    142
  • 氢给体数:
    2
  • 氢受体数:
    12

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:
    氯(二异丙基氨基)甲氧基膦2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosineN,N-二异丙基乙胺 作用下, 以 1,2-二氯乙烷 为溶剂, 反应 0.83h, 以95.4%的产率得到3-N-pivaloyl-2'-O-[1-(2-fluorophenyl)-4-methoxypiperidin-4-yl]-3'-O-(9-phenylxanthen-9-yl)adenosine-5'-O-(methyl N,N-diisopropylphosphoramidite)
    参考文献:
    名称:
    Solid-phase synthesis of branched RNA and branched DNA/RNA chimeras
    摘要:
    An effective method for synthesising branched oligonucleotides on solid phase in the 5' to 3' direction has been developed. Special branch-point monomers enable the synthesis of branched oligonucleotides which can have sequences of different length and base composition attached to the 2'-and 3'-hydroxyl groups of the branch point ribonucleoside. The branched oligonucleotides are assembled on commercial DNA synthesisers, the crude products are readily purified by reversed phase HPLC and the fully deprotected products are conveniently analysed by mass spectrometry. (C) 1997 Elsevier Science Ltd.
    DOI:
    10.1016/s0040-4020(97)00731-x
  • 作为产物:
    描述:
    5'-O-(tert-butyldiphenylsilyl)-2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 以92.9%的产率得到2'-O-<1-(2-fluorophenyl)-4-methoxypiperidin-4-yl>-3'-O-(9-phenylxanthen-9-yl)-6-N-pivaloyladenosine
    参考文献:
    名称:
    Sproat, Brian S.; Beijer, Barbro; Groetli, Morten, Journal of the Chemical Society. Perkin transactions I, 1994, # 4, p. 419 - 432
    摘要:
    DOI:
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文献信息

  • Sproat, Brian S.; Beijer, Barbro; Groetli, Morten, Journal of the Chemical Society. Perkin transactions I, 1994, # 4, p. 419 - 432
    作者:Sproat, Brian S.、Beijer, Barbro、Groetli, Morten、Ryder, Ursula、Morand, Kenneth L.、Lamond, Angus I.
    DOI:——
    日期:——
  • Solid-phase synthesis of branched RNA and branched DNA/RNA chimeras
    作者:Morten Grøtli、Ramon Eritja、Brian Sproat
    DOI:10.1016/s0040-4020(97)00731-x
    日期:1997.8
    An effective method for synthesising branched oligonucleotides on solid phase in the 5' to 3' direction has been developed. Special branch-point monomers enable the synthesis of branched oligonucleotides which can have sequences of different length and base composition attached to the 2'-and 3'-hydroxyl groups of the branch point ribonucleoside. The branched oligonucleotides are assembled on commercial DNA synthesisers, the crude products are readily purified by reversed phase HPLC and the fully deprotected products are conveniently analysed by mass spectrometry. (C) 1997 Elsevier Science Ltd.
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