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4-acetyl-1-(2-azido-2-deoxy-3,5-di-O-benzoyl-4-thio-β-D-arabino-pentofuranosyl)cytosine | 237406-96-1

中文名称
——
中文别名
——
英文名称
4-acetyl-1-(2-azido-2-deoxy-3,5-di-O-benzoyl-4-thio-β-D-arabino-pentofuranosyl)cytosine
英文别名
[(2R,3S,4S,5R)-5-(4-acetamido-2-oxopyrimidin-1-yl)-4-azido-3-benzoyloxythiolan-2-yl]methyl benzoate
4-acetyl-1-(2-azido-2-deoxy-3,5-di-O-benzoyl-4-thio-β-D-arabino-pentofuranosyl)cytosine化学式
CAS
237406-96-1
化学式
C25H22N6O6S
mdl
——
分子量
534.552
InChiKey
KBCSVRBIWMCTHX-FVTFTPSCSA-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):
    3.8
  • 重原子数:
    38
  • 可旋转键数:
    10
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    154
  • 氢给体数:
    1
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    4-acetyl-1-(2-azido-2-deoxy-3,5-di-O-benzoyl-4-thio-β-D-arabino-pentofuranosyl)cytosine 作用下, 以 甲醇 为溶剂, 反应 48.0h, 以79%的产率得到1-(2-azido-2-deoxy-4-thio-β-D-arabino-pentofuranosyl)cytosine
    参考文献:
    名称:
    An Alternative Synthesis of the Antineoplastic Nucleoside 4‘-ThioFAC and Its Application to the Synthesis of 4‘-ThioFAG and 4‘-Thiocytarazid
    摘要:
    Previously, we synthesized 4'-thioFAC, a novel antineoplastic cytosine nucleoside, by developing an original method. However, several problems remained. To overcome these problems, we have developed an alternative method far the synthesis of 4'-thionucleosides. In the original synthesis, carbons from C1 to C5 of D-glucose were used. The new method also starts from D-glucose but uses carbons closer to the tail (C2-C6). A dibenzoyl derivative obtained by this approach was brominated at the anomeric position to give a 1-bromide derivative. Fusion of the I-bromide and persilylated acetylcytosine, followed by deprotection, predominantly gave a beta-anomer of 4'-thioFAC. The reaction of 2,6-diaminopurine with the I-bromide in the presence of TMS triflate gave a glycosylated product in good yield. After deprotection, the resulting 1:1 anomeric mixture of free nucleosides was treated with adenosine deaminase to give a beta-anomer of 4'-thioFAG, a guanine congener of 4'-thioFAC, selectively. Using a similar approach, we synthesized 4'-thiocytarazid, which was not possible using the original method.
    DOI:
    10.1021/jo990958g
  • 作为产物:
    参考文献:
    名称:
    Synthetic Studies on 2′-Substituted-4′-thiocytidine Derivatives as Antineoplastic Agents
    摘要:
    As potential antineoplastic agents, we have synthesized 4'-thioFAC and 4'-thiocytarazid by developing an alternative synthetic method. 4'-ThioFAC showed potent antineoplastic activities in vivo as well as in vitro.
    DOI:
    10.1080/15257779908041569
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