[[(E)-4-[2-oxo-6-(4-pentylphenyl)furo[2,3-d]pyrimidin-3-yl]but-2-enyl]-(propan-2-yloxycarbonyloxymethoxy)phosphoryl]oxymethyl propan-2-yl carbonate | 1314531-95-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 呋喃[2,3-d]嘧啶
• 英文名称: [[(E)-4-[2-oxo-6-(4-pentylphenyl)furo[2,3-d]pyrimidin-3-yl]but-2-enyl]-(propan-2-yloxycarbonyloxymethoxy)phosphoryl]oxymethyl propan-2-yl carbonate
• CAS: 1314531-95-7
• 化学式: C₃₁H₄₁N₂O₁₁P
• 分子量: 648.647
• InChiKey: XLXZAUDLEZWJKS-MDZDMXLPSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6
• 重原子数：
  45
• 可旋转键数：
  21
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.48
• 拓扑面积：
  149
• 氢给体数：
  0
• 氢受体数：
  11

反应信息

• 作为产物：
  描述：

  N1-crotyl-5-((4-n-pentylphenyl)ethynyl)uracil 在 RuCl2(1,3-dimesityl-imidazolidin-2-yl)(PCy3)(=CHPh) 、 copper(l) iodide 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 为溶剂， 反应 21.0h， 生成 、 [[(E)-4-[2-oxo-6-(4-pentylphenyl)furo[2,3-d]pyrimidin-3-yl]but-2-enyl]-(propan-2-yloxycarbonyloxymethoxy)phosphoryl]oxymethyl propan-2-yl carbonate
  参考文献：
  名称：

  Expeditious convergent procedure for the preparation of bis(POC) prodrugs of new (E)-4-phosphono-but-2-en-1-yl nucleosides

  摘要：

  A series of unsaturated acyclonucleoside bis(POC) prodrugs of E configuration were synthesized through an expeditious, highly efficient and stereoselective one-step procedure from corresponding bis(POC)allylphosphonate through Ru catalyzed cross-coupling metathesis reaction. The [RuCl(2)(PCy(3))(SIPr)(Inde-nylidene)] and [RuCl(2)(PCy(3))(IMes)(benzylidene)] catalysts were employed; the unsaturated ANP were used bore C5-halovinyl uracil, C5-dihalovinyluracil or furanopyrimidine motifs. The chemical cleavage of biolabile (POC) group is a useful pathway to acid phosphonate derivatives. (C) 2011 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2011.05.017

文献信息

• Expeditious convergent procedure for the preparation of bis(POC) prodrugs of new (E)-4-phosphono-but-2-en-1-yl nucleosides
  作者：Aurélien Montagu、Ugo Pradére、Vincent Roy、Steven P. Nolan、Luigi A. Agrofoglio

  DOI：10.1016/j.tet.2011.05.017

  日期：2011.7

  A series of unsaturated acyclonucleoside bis(POC) prodrugs of E configuration were synthesized through an expeditious, highly efficient and stereoselective one-step procedure from corresponding bis(POC)allylphosphonate through Ru catalyzed cross-coupling metathesis reaction. The [RuCl(2)(PCy(3))(SIPr)(Inde-nylidene)] and [RuCl(2)(PCy(3))(IMes)(benzylidene)] catalysts were employed; the unsaturated ANP were used bore C5-halovinyl uracil, C5-dihalovinyluracil or furanopyrimidine motifs. The chemical cleavage of biolabile (POC) group is a useful pathway to acid phosphonate derivatives. (C) 2011 Elsevier Ltd. All rights reserved.