1-(3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-β-L-arabino-hexofuranosyl)thymine | 142138-08-7

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 1-(3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-β-L-arabino-hexofuranosyl)thymine
• 英文别名: 1-[(2S,4S,5R)-5-[(1S)-1-hydroxyethyl]-4-(1,2,4-triazol-1-yl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione
• CAS: 142138-08-7
• 化学式: C₁₃H₁₇N₅O₄
• 分子量: 307.309
• InChiKey: UUKCXTBOFZZPRV-NAKRPEOUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -0.7
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.54
• 拓扑面积：
  110
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为产物：
  描述：

  1-<5-O-acetyl-3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-β-L-arabino-hexofuranosyl>thymine 在 甲胺 作用下， 以 乙醇 为溶剂， 反应 24.0h， 以85%的产率得到1-(3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-β-L-arabino-hexofuranosyl)thymine
  参考文献：
  名称：

  Synthesis of 1-(3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-L-arabino-hexofuranosyl)uracils via an ?,?-unsaturated aldehydrohexose

  摘要：

  Mercuric catalyzed hydrolysis of acetylated L-rhamnal 1 gave the alpha,beta-unsaturated aldehyde 2. 1,2,4-Triazole was coupled, in a Michael type addition reaction, to 2 at C-3 in the presence of 1,8-diazabicyclo [5.4.0]undec-7-ene (DBU) to give, after acetylation at the anomeric center, an anomeric mixture of 1,5-di-O-acetyl-3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-L-arabino-hexofuranose (3). Reaction of 3 with silylated 2,4-dihydroxypyrimidines 4 in the presence of trimethylsilyl triflate as catalyst followed by deprotection with 33% methylamine in absolute ethanol afforded the corresponding nucleosides 7 and 8.

  DOI：

  10.1007/bf00810947

文献信息

• Synthesis of 1-(3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-L-arabino-hexofuranosyl)uracils via an ?,?-unsaturated aldehydrohexose
  作者：Krzysztof Walczak、Jesper Wengel、Erik B. Pedersen

  DOI：10.1007/bf00810947

  日期：1992.4

  Mercuric catalyzed hydrolysis of acetylated L-rhamnal 1 gave the alpha,beta-unsaturated aldehyde 2. 1,2,4-Triazole was coupled, in a Michael type addition reaction, to 2 at C-3 in the presence of 1,8-diazabicyclo [5.4.0]undec-7-ene (DBU) to give, after acetylation at the anomeric center, an anomeric mixture of 1,5-di-O-acetyl-3-(1,2,4-triazol-1-yl)-2,3,6-trideoxy-L-arabino-hexofuranose (3). Reaction of 3 with silylated 2,4-dihydroxypyrimidines 4 in the presence of trimethylsilyl triflate as catalyst followed by deprotection with 33% methylamine in absolute ethanol afforded the corresponding nucleosides 7 and 8.