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11-(2-methoxyethylsulfanyl)-5,6-dihydronaphtho[1',2':4,5]thieno[2,3-d]pyrimidine

中文名称
——
中文别名
——
英文名称
11-(2-methoxyethylsulfanyl)-5,6-dihydronaphtho[1',2':4,5]thieno[2,3-d]pyrimidine
英文别名
16-(2-Methoxyethylsulfanyl)-11-thia-13,15-diazatetracyclo[8.7.0.02,7.012,17]heptadeca-1(10),2,4,6,12(17),13,15-heptaene
11-(2-methoxyethylsulfanyl)-5,6-dihydronaphtho[1',2':4,5]thieno[2,3-d]pyrimidine化学式
CAS
——
化学式
C17H16N2OS2
mdl
——
分子量
328.459
InChiKey
ZDEHQXSEBHVZAR-UHFFFAOYSA-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):
    4.2
  • 重原子数:
    22
  • 可旋转键数:
    4
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    88.6
  • 氢给体数:
    0
  • 氢受体数:
    5

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:
    5,6,10-trihydronaphtho[1',2':4,5]thieno[2,3-d]pyrimidin-11-one 在 吡啶diphosphorus pentasulfide 、 sodium hydride 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 生成 11-(2-methoxyethylsulfanyl)-5,6-dihydronaphtho[1',2':4,5]thieno[2,3-d]pyrimidine
    参考文献:
    名称:
    Synthesis and Antiviral Screening of Some Thieno[2,3-d]Pyrimidine Nucleosides
    摘要:
    Some cyclic and acyclic nucleosides of thieno[2,3-d]-pyrimidine derivatives were synthesized via the reaction of compounds 1 and 2 or 3 and 4 with 2-chloroethyl methyl ether or 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide. Nucleosides 9, 10, 15, and 16 were tested as antiviral agents against herpes simplex virus type-1 ( HSV-1) and hepatitis-A virus ( HAV). Compound 15 showed the highest effect on HSV-1 than the other three compounds, while the four tested compounds did not show any activity against HAV.
    DOI:
    10.1080/15257770500377730
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文献信息

  • Synthesis and Antiviral Screening of Some Thieno[2,3-<i>d</i>]Pyrimidine Nucleosides
    作者:A. E. Rashad、M. A. Ali
    DOI:10.1080/15257770500377730
    日期:2006.1
    Some cyclic and acyclic nucleosides of thieno[2,3-d]-pyrimidine derivatives were synthesized via the reaction of compounds 1 and 2 or 3 and 4 with 2-chloroethyl methyl ether or 2,3,4,6-tetra-O-acetyl-alpha-D-glucopyranosyl bromide. Nucleosides 9, 10, 15, and 16 were tested as antiviral agents against herpes simplex virus type-1 ( HSV-1) and hepatitis-A virus ( HAV). Compound 15 showed the highest effect on HSV-1 than the other three compounds, while the four tested compounds did not show any activity against HAV.
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