6-chloro-9-(5'-O-acetyl-2',3'-dideoxy-β-D-glycero-pent-2'-enofuranosyl)purine | 389128-20-5

• 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: 6-chloro-9-(5'-O-acetyl-2',3'-dideoxy-β-D-glycero-pent-2'-enofuranosyl)purine
• CAS: 389128-20-5
• 化学式: C₁₂H₁₁ClN₄O₃
• 分子量: 294.697
• InChiKey: NIKGNVHURYKMTD-DTWKUNHWSA-N

物化性质

• 沸点：
  481.3±55.0 °C(Predicted)
• 密度：
  1.60±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.5
• 重原子数：
  20.0
• 可旋转键数：
  3.0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  79.13
• 氢给体数：
  0.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  6-chloro-9-(5'-O-acetyl-2',3'-dideoxy-β-D-glycero-pent-2'-enofuranosyl)purine 在 palladium on activated charcoal 氨 、 水 、 氢气 、 三乙胺 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 14.0h， 生成 2',3'-dideoxy-5'-O-dihydroxyphosphoryl-N⁶-[1-(4-aminobutyl)]adenosine
  参考文献：
  名称：

  Synthesis of haptens for the development of immunoassays for the monitoring of intracellular anti-HIV nucleosides and nucleotides

  摘要：

  A series of nine modified dideoxynucleosides and dideoxynucleotides has been synthesized for preparing antigenic conjugates with keyhole lympet haemocyanin in order to produce specific antibodies, and develop immunoassays. Derivatives of ddI, ddA, d4T, 3TC, and the corresponding 5 ' -O-monophosphates were designed incorporating an amino spacer at the base for conjugation with the proteinic antigenic carrier. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(01)00800-6
• 作为产物：
  描述：

  乙酸酐 、 肌苷 以104 mg的产率得到6-chloro-9-(5'-O-acetyl-2',3'-dideoxy-β-D-glycero-pent-2'-enofuranosyl)purine
  参考文献：
  名称：

  Synthesis of haptens for the development of immunoassays for the monitoring of intracellular anti-HIV nucleosides and nucleotides

  摘要：

  A series of nine modified dideoxynucleosides and dideoxynucleotides has been synthesized for preparing antigenic conjugates with keyhole lympet haemocyanin in order to produce specific antibodies, and develop immunoassays. Derivatives of ddI, ddA, d4T, 3TC, and the corresponding 5 ' -O-monophosphates were designed incorporating an amino spacer at the base for conjugation with the proteinic antigenic carrier. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(01)00800-6

文献信息

• CONVENIENT SYNTHESIS OF FLUORINATED NUCLEOSIDES WITH PERFLUOROALKANESULFONYL FLUORIDES
  作者：Satoshi Takamatsu、Satoshi Katayama、Naoko Hirose、Etienne De Cock、Geert Schelkens、Marc Demillequand、Jozef Brepoels、Kunisuke Izawa

  DOI：10.1081/ncn-120016572

  日期：2002.12.31

  Perfluoroalkanesulfonyl fluorides are effective dehydroxy-fluorination agents for the hydroxyl group at the sugar moiety of nucleoside derivatives and give the corresponding fluorinated nucleosides in good yield with an inversion of configuration in a single step.