1(5-O-tert-butyldimethylsilyl-1-cyano-β-D-ribofuranosyl)thymine | 152039-38-8

• 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(5-O-tert-butyldimethylsilyl-1-cyano-β-D-ribofuranosyl)thymine
• 英文别名: (2R,3R,4S,5R)-5-[[tert-butyl(dimethyl)silyl]oxymethyl]-3,4-dihydroxy-2-(5-methyl-2,4-dioxopyrimidin-1-yl)oxolane-2-carbonitrile
• CAS: 152039-38-8
• 化学式: C₁₇H₂₇N₃O₆Si
• 分子量: 397.503
• InChiKey: LWGKAYAVFAQRFM-HPTBWKMGSA-N

物化性质

• 密度：
  1.27±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  0.16
• 重原子数：
  27
• 可旋转键数：
  5
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.71
• 拓扑面积：
  132
• 氢给体数：
  3
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  1(5-O-tert-butyldimethylsilyl-1-cyano-β-D-ribofuranosyl)thymine 在 四丁基氟化铵 、 二正丁基氧化锡 、 亚磷酸三乙酯 作用下， 以 四氢呋喃 、 乙腈 为溶剂， 反应 13.25h， 生成 1(1-cyano-2,3-dideoxy-β-D-glycero-pent-2-enofuranosyl)thymine
  参考文献：
  名称：

  Synthesis and structure determination of the first 1′-C-cyano-β-D-nucleosides

  摘要：

  The 1'-cyano -2',3'-D-unsaturated nucleoside 8 was synthesised according to the following steps. Photobromination of the ribofuranosyl cyanide 1 using N-bromosuccinimide (NBS) as a radical source gave the two isomers of the new C-1 gem disubstituted sugar 2. Its condensation with silylated thymine afforded the blocked nucleoside 3, the stereochemistry and molecular shape of which were deduced from NMR studies and molecular simulation. After deprotection of 3 into 4, thiocarbonylation of the silylated derivative 5, followed by olefination of 6, led to 7 which was deblocked to the 1'-cyano substituted d4T 8.

  DOI：

  10.1016/s0040-4020(01)96264-7
• 作为产物：
  描述：

  O,O-二(三甲基甲硅烷基)胸苷 在 咪唑 、 ammonium hydroxide 、 氰化汞 作用下， 以 甲醇 、 硝基甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 96.0h， 生成 1(5-O-tert-butyldimethylsilyl-1-cyano-β-D-ribofuranosyl)thymine
  参考文献：
  名称：

  Synthesis and structure determination of the first 1′-C-cyano-β-D-nucleosides

  摘要：

  The 1'-cyano -2',3'-D-unsaturated nucleoside 8 was synthesised according to the following steps. Photobromination of the ribofuranosyl cyanide 1 using N-bromosuccinimide (NBS) as a radical source gave the two isomers of the new C-1 gem disubstituted sugar 2. Its condensation with silylated thymine afforded the blocked nucleoside 3, the stereochemistry and molecular shape of which were deduced from NMR studies and molecular simulation. After deprotection of 3 into 4, thiocarbonylation of the silylated derivative 5, followed by olefination of 6, led to 7 which was deblocked to the 1'-cyano substituted d4T 8.

  DOI：

  10.1016/s0040-4020(01)96264-7

文献信息

• Synthesis and structure determination of the first 1′-C-cyano-β-D-nucleosides
  作者：Valérie Uteza、Guo-Rong Chen、Jérémie Le Quan Tuoi、Gérard Descotes、Bernard Fenet、Annie Grouiller

  DOI：10.1016/s0040-4020(01)96264-7

  日期：1993.9

  The 1'-cyano -2',3'-D-unsaturated nucleoside 8 was synthesised according to the following steps. Photobromination of the ribofuranosyl cyanide 1 using N-bromosuccinimide (NBS) as a radical source gave the two isomers of the new C-1 gem disubstituted sugar 2. Its condensation with silylated thymine afforded the blocked nucleoside 3, the stereochemistry and molecular shape of which were deduced from NMR studies and molecular simulation. After deprotection of 3 into 4, thiocarbonylation of the silylated derivative 5, followed by olefination of 6, led to 7 which was deblocked to the 1'-cyano substituted d4T 8.