(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate | 1260177-41-0

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘌呤核苷
• 英文名称: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
• 英文别名: 2-chloro-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)-9H-purine；[(2R,3R,4R,5R)-3,4-diacetyloxy-5-(2-chloropurin-9-yl)oxolan-2-yl]methyl acetate
• CAS: 1260177-41-0
• 化学式: C₁₆H₁₇ClN₄O₇
• 分子量: 412.787
• InChiKey: SGJGXDVELVNMPT-RGCMKSIDSA-N

物化性质

• 沸点：
  517.8±60.0 °C(Predicted)
• 密度：
  1.62±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.6
• 重原子数：
  28
• 可旋转键数：
  8
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  132
• 氢给体数：
  0
• 氢受体数：
  10

反应信息

• 作为反应物：
  描述：

  (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate 在 氨 作用下， 以 乙醇 、 氯仿 为溶剂， 以204 mg的产率得到2-Chloro-purine riboside
  参考文献：
  名称：

  Investigations into the Origin of the Molecular Recognition of Several Adenosine Deaminase Inhibitors

  摘要：

  Inhibitors of adenosine deaminase (ADA, EC 3 5 4 4) are potential therapeutic agents for the treatment of various health disorders Several highly potent inhibitors were previously identified, yet they exhibit unacceptable toxicities We performed a SAR study involving a series of C2 or C8 substituted purine-riboside analogues with a view to discover less potent inhibitors with a lesser toxicity We found that any substitution at C8 position of nebularine resulted in total loss of activity toward calf intestinal ADA However several 2-substituted-adenosine, 8-aza-adenosine, and nebularine analogues exhibited inhibitory activity Specifically, 2-Cl-purine riboside, 8-aza-2-thiohexyl adenosine, 2-thiohexyl adenosine, and 2-MeS-purine riboside were found to be competitive inhibitors of ADA with K-i values of 25, 22, 6, and 3 mu M, respectively We concluded that electronic parameters are not major recognition determinants of ADA but rather steric parameters A C2 substituent which fits ADA hydrophobic pocket and improves H-bonding with the enzyme makes a good inhibitor In addition, a gg rotamer about C4'-C5' bond is apparently an important recognition determinant

  DOI：

  10.1021/jm101286g
• 作为产物：
  描述：

  (2R,3R,4R,5R)-4-(acetyloxy)-2-[(acetyloxy)methyl]-5-(2,6-dichloro-9H-purin-9-yl)tetrahydro-3-furanyl acetate 在 水 、 氧气 、 一水合肼 、 copper(II) sulfate 作用下， 以 乙醇 为溶剂， 反应 8.0h， 生成 (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(2-chloro-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
  参考文献：
  名称：

  Efficient synthesis of nebularine and vidarabine via dehydrazination of (hetero)aromatics catalyzed by CuSO₄in water

  摘要：

  首次在催化量的CuSO4存在下实现了一步简单的脱氢反应。以CuSO4 (2 mol%)为催化剂，水为溶剂，脱氢产物获得了良好的产率（66-95%）。此外，成功合成了药物 nebularine 和 Vidarabine，并且 Vidarabine 可在0.923公斤规模生产，显示出良好的工业应用潜力。

  DOI：

  10.1039/c3gc41658e

文献信息

• Synthesis of cycloalkyl substituted purine nucleosides via a metal-free radical route
  作者：Dong-Chao Wang、Ran Xia、Ming-Sheng Xie、Gui-Rong Qu、Hai-Ming Guo

  DOI：10.1039/c6ob00596a

  日期：——

  An efficient route to synthesize cycloalkyl substituted purine nucleosides was developed. This metal-free C-H activation was accomplished by tBuOOtBu initiated radical reaction. By adjusting the amount of tBuOOtBu and reaction...

  开发了合成环烷基取代的嘌呤核苷的有效途径。这种无金属的CH活化是通过tBuOOtBu引发的自由基反应完成的。通过调整tBuOOtBu的量和反应...
• Radical Route for the Alkylation of Purine Nucleosides at C6 via Minisci Reaction
  作者：Ran Xia、Ming-Sheng Xie、Hong-Ying Niu、Gui-Rong Qu、Hai-Ming Guo

  DOI：10.1021/ol4033336

  日期：2014.1.17

  A highly regioselective Minisci reaction with the decarboxylative alkylation of purine nucleosides under mild conditions was developed. With 5 mol % AgNO3 as a catalyst and (NH4)2S2O8 as an oxidant, a series of purine nucleosides including ribosyl, deoxyribosyl, arabinosyl purine nucleosides worked well with primary, secondary, and tertiary aliphatic carboxylic acids.

  开发了在温和条件下具有嘌呤核苷脱羧烷基化的高度区域选择性Minisci反应。以5 mol％的AgNO 3为催化剂，以（NH 4）2 S 2 O 8为氧化剂，一系列嘌呤核苷，包括核糖基，脱氧核糖基，阿拉伯糖基嘌呤核苷，与伯，仲和叔脂肪族羧酸配合得很好。