1-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)uracil | 4348-70-3

• 分子结构分类: 有机化合物 - 核苷、核苷酸和类似物 - 嘧啶核苷
• 英文名称: 1-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)uracil
• 英文别名: (2R,3R,4S,5S)-2-((benzoyloxy)methyl)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)tetrahydrofuran-3,4-diyl dibenzoate；1-<2.3.5-Tri-O-benzoyl-α-D-arabinofuranosyl>-uracil；1-(tri-O-benzoyl-α-D-arabinofuranosyl)-1H-pyrimidine-2,4-dione；[(2R,3R,4S,5S)-3,4-dibenzoyloxy-5-(2,4-dioxopyrimidin-1-yl)oxolan-2-yl]methyl benzoate
• CAS: 4348-70-3
• 化学式: C₃₀H₂₄N₂O₉
• 分子量: 556.529
• InChiKey: MPYUTOYNCCRZAC-BPHNFWMXSA-N

物化性质

• 密度：
  1.44±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.5
• 重原子数：
  41
• 可旋转键数：
  11
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.17
• 拓扑面积：
  138
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  1-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)uracil 在 吡啶 、 4-二甲氨基吡啶 、 四丁基氟化铵 、 sodium methylate 、 溶剂黄146 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 为溶剂， 反应 68.75h， 生成 1-{5-O-(4,4'-dimethoxytrityl)-2-O-[2-(4-nitrophenyl)ethoxycarbonyl]-α-D-arabinofuranosyl}uracil
  参考文献：
  名称：

  Nucleotides. LXXIV Synthesis of a-D-Arabino-oligonucleotides

  摘要：

  The 5 alpha-D-arabinofuranosylnucleosides alpha-araU (15), alpha-araT (18), alpha-araC (22), alpha-araA (25), and alpha-araG (28) have been synthesized by the modified silyl-method. The amino groups at the nucleobases and the 2'-hydroxy group at the sugar moiety were protected by the 2-(4-nitro-phenyl) ethoxycarbonyl (npeoc) group (37-40) and the amide function in alpha-araG was additionally blocked by the 2-(4-nitrophenyl)ethyl group (63) to improve solubility in organic solvents. Mono-and dimethoxytritylation of the 5'-OH group was performed in the usual manner to give 41-48, 64, and 65 in high yields and further substitution of the 3'-OH group led to the monomeric building blocks 66-75 as well as the 3'-O-succinoyl derivatives 76-85 functioning as starting units in solid-support oligonucleotide synthesis. A large number of oligo-alpha-arabinonucleotides have been prepared on modified CPG-material applying the npeoc/npe strategy as a very efficient synthetic tool for highly purified, homogenous oligomers. Hybridizations between alpha-arabinonucleotide strands revealed in analogy to earlier findings an antiparallel orientation whereas the combination of an oligo-alpha-D-arabinonucleotide with a complementary oligo-2'-deoxy-beta-D-ribofuranosylnucleotide showed base-pairing only if a parallel polarity was present. The advantages in oligo-alpha-arabinonucleotide synthesis were furthermore demonstrated by the synthesis of the t alpha-ANA(his) a structural analog of the natural tRNA(his) of the phage T5.

  DOI：

  10.1080/15257770500267113
• 作为产物：
  描述：

  1-O-methyl-2,3,5-tri-O-benzoylarabinofuranose 在 N,O-双三甲硅基乙酰胺 、 硫酸 作用下， 以 乙酸乙酯 、 乙腈 为溶剂， 反应 6.5h， 生成 1-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)uracil
  参考文献：
  名称：

  [EN] MODIFIED OLIGOMERIC COMPOUNDS AND USES THEREOF
  [FR] COMPOSÉS OLIGOMÈRES MODIFIÉS ET LEURS UTILISATIONS

  摘要：

  本公开提供了包含至少一种立体非标准核苷酸的修饰寡核苷酸的寡聚化合物。包括由12-30个连接的核苷酸组成的修饰寡核苷酸的寡聚化合物，其中修饰寡核苷酸的至少一个核苷酸是立体非标准核苷酸；且所述寡聚化合物选自RNAi化合物、修饰CRISPR化合物和人工mRNA化合物。

  公开号：

  WO2021030763A1

文献信息

• A Procedure for Facile Synthesis of Nucleosides Using N, O-Bistrimethylsilylacetamide in the Presence of Natural Phosphate Coated with Potassium Iodide
  作者：Laila Baddi、Michael Smietana、Said Sebti、Jean-Jacques Vasseur、Hassan B. Lazrek

  DOI：10.2174/157017810791112441

  日期：2010.4.1

  yields under mild conditions by N-glycosylation of 1-O-acetyl D/L- arabino, and xylofuranose, with silylated nucleobases (uracil, thymine and 6- azauracil) in acetonitrile using natural phosphate (NP) coated with potassium iodide in BSA as catalyst.

  通过1-O-乙酰基D / L-阿拉伯糖和木呋喃糖的N-糖基化和甲硅烷基化的核碱基（尿嘧啶，胸腺嘧啶）在温和条件下以高收率合成了几种α-D/ L-阿拉伯糖苷和β-D/ L-木糖苷使用在BSA中用碘化钾包被的天然磷酸盐（NP）作为催化剂，在乙腈中加入6-氮杂尿嘧啶和6-氮杂嘧啶）。
• Condensation of 1-Fluorofuranoses and Silylated Nucleobases Catalyzed by Tetrafluorosilane
  作者：Ryoji Noyori、Masahiko Hayashi

  DOI：10.1246/cl.1987.57

  日期：1987.1.5

  The title reaction provides a generally useful tool for nucleoside synthesis. The stereoselectivities are highly influenced by the fluoride substrates, and steric course of the reaction of O-benzylated ribofuranosyl fluoride is solvent dependent.

  标题反应为核苷合成提供了一个普遍有用的工具。立体选择性受氟化物底物的影响很大，并且 O-苄基化呋喃核糖基氟反应的空间过程是溶剂依赖性的。
• MODIFIED OLIGOMERIC COMPOUNDS AND USES THEREOF
  申请人：Ionis Pharmaceuticals, Inc.

  公开号：EP4013428A1

  公开（公告）日：2022-06-22