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5'-O-t-butyldimethylsilyl-3'-carbomethoxymethyl-4-desamino-4-azido-2',3'-dideocytidine | 161045-33-6

中文名称
——
中文别名
——
英文名称
5'-O-t-butyldimethylsilyl-3'-carbomethoxymethyl-4-desamino-4-azido-2',3'-dideocytidine
英文别名
methyl 2-[(2S,3R,5R)-5-(4-azido-2-oxopyrimidin-1-yl)-2-[[tert-butyl(dimethyl)silyl]oxymethyl]oxolan-3-yl]acetate
5'-O-t-butyldimethylsilyl-3'-carbomethoxymethyl-4-desamino-4-azido-2',3'-dideocytidine化学式
CAS
161045-33-6
化学式
C18H29N5O5Si
mdl
——
分子量
423.544
InChiKey
AGSCXXANLZBFHJ-UMVBOHGHSA-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):
    3.67
  • 重原子数:
    29
  • 可旋转键数:
    9
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.72
  • 拓扑面积:
    91.8
  • 氢给体数:
    0
  • 氢受体数:
    6

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
  • 下游产品
    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:
    5'-O-t-butyldimethylsilyl-3'-carbomethoxymethyl-4-desamino-4-azido-2',3'-dideocytidine 在 sodium azide 、 四丁基氟化铵苯硫酚三乙胺 、 tin(ll) chloride 作用下, 以 四氢呋喃吡啶二氯甲烷N,N-二甲基甲酰胺乙腈 为溶剂, 反应 43.0h, 生成 5'-azido-3'-carbomethoxymethyl-4-N-benzoyl-2',3',5'-trideoxycytidine
    参考文献:
    名称:
    Synthesis of Deoxycytidine (dC) Building Blocks for Amide-Linked Dimers or Oligomers: Example of a Deoxycytidine-amide-thymidine Dimer
    摘要:
    5'-Azido-3'-carbomethoxymethyl-4-N-benzoyl-2',3',5'-trideoxy-cytidine 17 and 5'-O-t-butyldimethylsilyl-3'-carboxymethyl-4-N-benzoyl-2',3'-dideocytidine 22 were efficiently synthesized from 2'-deoxyuridine via a new method which transformed the uracil heterocycle to 4-N-benzoylcytosine (four steps, 60 % overall yield). The amide-linked deoxycytidine-thymidine dimer analog was synthesized.
    DOI:
    10.1080/15257779408010666
  • 作为产物:
    描述:
    5'-O-t-butyldimethylsilyl-3'-(2''-oxoethyl)-2',3'-dideoxyuridine 在 4-二甲氨基吡啶重铬酸吡啶 、 sodium azide 、 三乙胺 作用下, 以 1,2-二氯乙烷N,N-二甲基甲酰胺 为溶剂, 反应 6.0h, 生成 5'-O-t-butyldimethylsilyl-3'-carbomethoxymethyl-4-desamino-4-azido-2',3'-dideocytidine
    参考文献:
    名称:
    Synthesis of Deoxycytidine (dC) Building Blocks for Amide-Linked Dimers or Oligomers: Example of a Deoxycytidine-amide-thymidine Dimer
    摘要:
    5'-Azido-3'-carbomethoxymethyl-4-N-benzoyl-2',3',5'-trideoxy-cytidine 17 and 5'-O-t-butyldimethylsilyl-3'-carboxymethyl-4-N-benzoyl-2',3'-dideocytidine 22 were efficiently synthesized from 2'-deoxyuridine via a new method which transformed the uracil heterocycle to 4-N-benzoylcytosine (four steps, 60 % overall yield). The amide-linked deoxycytidine-thymidine dimer analog was synthesized.
    DOI:
    10.1080/15257779408010666
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文献信息

  • Synthesis of Deoxycytidine (dC) Building Blocks for Amide-Linked Dimers or Oligomers: Example of a Deoxycytidine-amide-thymidine Dimer
    作者:Evelyne Grunder-Klotz、George Just
    DOI:10.1080/15257779408010666
    日期:1994.9
    5'-Azido-3'-carbomethoxymethyl-4-N-benzoyl-2',3',5'-trideoxy-cytidine 17 and 5'-O-t-butyldimethylsilyl-3'-carboxymethyl-4-N-benzoyl-2',3'-dideocytidine 22 were efficiently synthesized from 2'-deoxyuridine via a new method which transformed the uracil heterocycle to 4-N-benzoylcytosine (four steps, 60 % overall yield). The amide-linked deoxycytidine-thymidine dimer analog was synthesized.
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