4(S)-(2-amino-6-chloro-9H-purin-9-yl)tetrahydro-2(S)-furanmethanol | 151223-89-1

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 咪唑并嘧啶类
• 英文名称: 4(S)-(2-amino-6-chloro-9H-purin-9-yl)tetrahydro-2(S)-furanmethanol
• 英文别名: (2R-cis)-4-(2-amino-6-chloro-9H-purin-9-yl)tetrahydro-2-furanmethanol；[(2S,4S)-4-(2-amino-6-chloropurin-9-yl)oxolan-2-yl]methanol
• CAS: 151223-89-1
• 化学式: C₁₀H₁₂ClN₅O₂
• 分子量: 269.691
• InChiKey: GFUMLXGMHGHWEK-WDSKDSINSA-N

物化性质

• 沸点：
  594.9±60.0 °C(predicted)
• 密度：
  1.88±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  -0.2
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  99.1
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  4(S)-(2-amino-6-chloro-9H-purin-9-yl)tetrahydro-2(S)-furanmethanol 在 palladium on activated charcoal 氢气 、 sodium acetate 作用下， 以 乙醇 为溶剂， 反应 24.0h， 以78%的产率得到(2R-cis)-4-(2-amino-9H-purin-9-yl)tetrahydro-2-furanmethanol
  参考文献：
  名称：

  Synthesis and anti-HIV activity of isonucleosides

  摘要：

  A series of isomeric 2',3'-dideoxynucleosides which contains a modified carbohydrate moiety has been prepared. This class of compounds was designed to mimic the activity of known anti-HIV dideoxynucleosides, while imparting enhanced chemical and enzymatic stability. Isonucleosides containing the standard heterocyclic bases (A, C, G, T) were synthesized via nucleophilic addition of the base to an isomeric sugar unit. Modified derivatives were generated by manipulation of the intact isonucleoside. Two of the compounds prepared, iso-ddA (1) and iso-ddG (6), exhibit significant and selective anti-HIV activity, as well as beneficial hydrolytic stability.

  DOI：

  10.1021/jm00091a001
• 作为产物：
  描述：

  5-O-benzoyl-α-D-xylofuranose 在 盐酸 、 三乙基硅烷 、 三甲基氯硅烷 、 18-冠醚-6 、 偶氮二异丁腈 、 三氟甲磺酸三甲基硅酯 、 氨 、 potassium carbonate 作用下， 以 吡啶 、 甲醇 、 乙醇 、 二氯甲烷 、 N,N-二甲基甲酰胺 、 甲苯 为溶剂， 反应 142.0h， 生成 4(S)-(2-amino-6-chloro-9H-purin-9-yl)tetrahydro-2(S)-furanmethanol
  参考文献：
  名称：

  Novel isomeric dideoxynucleosides as potential antiviral agents

  摘要：

  Novel isomeric dideoxynucleosides with S,S absolute stereochemistry and involving the transposition of the base moiety from the normal 1'- to the 2'-position have been regiospecifically and stereospecifically synthesized. The synthetic approaches involved either direct coupling with inversion at the 2-position of a preformed dideoxygenated sugar using the base moiety as nucleophile (for purine isodideoxynucleosides) or construction of the base moiety onto a stereochemically defined amino sugar precursor (pyrimidine isodideoxynucleosides). These compounds possess extremely high stability with respect to ''glycosidic'' bond cleavage and enzymatic deamination. Antiviral data suggest that the most active compound was levorotatory S,S-isodideoxyadenosine.

  DOI：

  10.1016/s0040-4020(01)85259-5