2-amino-8-[3,5-bis-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-4-[2-(4-nitrophenyl)ethoxy]pteridin-7(8H)-one | 195821-72-8

• 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: 2-amino-8-[3,5-bis-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-4-[2-(4-nitrophenyl)ethoxy]pteridin-7(8H)-one
• CAS: 195821-72-8
• 化学式: C₃₃H₂₆Cl₂N₆O₉
• 分子量: 721.51
• InChiKey: KTEYRANFSWYSSF-ZWEKWIFMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.98
• 重原子数：
  50.0
• 可旋转键数：
  11.0
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.21
• 拓扑面积：
  200.89
• 氢给体数：
  1.0
• 氢受体数：
  14.0

反应信息

• 作为反应物：
  描述：

  2-amino-8-[3,5-bis-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-4-[2-(4-nitrophenyl)ethoxy]pteridin-7(8H)-one 在 氰化钠 作用下， 以 甲醇 为溶剂， 以65%的产率得到2-amino-8-[2-deoxy-β-D-ribofuranosyl]-4-[2-(4-nitrophenyl)ethoxy]pteridin-7(8H)-one
  参考文献：
  名称：

  Synthesis of 8-(2-Deoxy-β-D-Ribofuranosyl)-Isoxanthopterins New Fluorescent Analogs of 2′-Deoxyguanosine

  摘要：

  We have synthesized isoxanthopterin and 6-phenylisoxanthopterin nucleosides in form of their 5'-O-dimethoxytritylated 3'-phosphoramidites to be used as fluorescence markers directly in the synthesis of oligonucleotides by a machine-aided solid-support approach. The preparation of the monomers and some results of the oligonucleotide synthesis will be described.

  DOI：

  10.1080/07328319708002965
• 作为产物：
  描述：

  1-氯-2-脱氧-3,5-二-O-对氯苯甲酰基-D-核糖 在 偶氮二甲酸二异丙酯 、 氨 、 二甲基二环氧乙烷 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 、 三苯基膦 作用下， 以 1,4-二氧六环 、 二氯甲烷 、 丙酮 、 乙腈 为溶剂， 反应 5.0h， 生成 2-amino-8-[3,5-bis-O-(4-chlorobenzoyl)-2-deoxy-β-D-ribofuranosyl]-4-[2-(4-nitrophenyl)ethoxy]pteridin-7(8H)-one
  参考文献：
  名称：

  Nucleotides, Part LXIX, Synthesis of Phosphoramidite Building Blocks of IsoxanthopterinN8-(2′-Deoxy-β-D-ribonucleosides): New Fluorescence Markers for Oligonucleotide Synthesis

  摘要：

  The chemical synthesis of isoxanthopterin and 6-phenylisoxanthopterin N-8-(2'-deoxy-beta -D-ribofuranosyl nucleosides) is described as well as their conversion into suitably protected 3'-phosphoramidite building blocks to be used as marker molecules for DNA synthesis. Applying the npe/npeoc (=2-(4-nitrophenyl)ethyl/[2-(4-nitrophenyl)ethoxy]carbonyl) strategy, we used the new building blocks in the preparation of oligonucleotides by an automated solid-support approach, The hybridization properties of a series of labelled oligomers were studied by UV-melting techniques. It was found that the newly synthesized markers only slightly interfered with the abilities of the labelled oligomers to form stable duplexes with complementary oligonucleotides.

  DOI：

  10.1002/1522-2675(20010815)84:8<2330::aid-hlca2330>3.0.co;2-u