(3R)-3-tert-butyl(dimethyl)silyloxybutyl chlorocarbonate | 752235-84-0

• 分子结构分类: 有机化合物 - 有机金属化合物 - 有机类金属化合物
• 英文名称: (3R)-3-tert-butyl(dimethyl)silyloxybutyl chlorocarbonate
• 英文别名: [(3R)-3-[tert-butyl(dimethyl)silyl]oxybutyl] carbonochloridate
• CAS: 752235-84-0
• 化学式: C₁₁H₂₃ClO₃Si
• 分子量: 266.84
• InChiKey: JGLMEJBHHCVUPW-SECBINFHSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.16
• 重原子数：
  16
• 可旋转键数：
  7
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.91
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  (3R)-3-tert-butyl(dimethyl)silyloxybutyl chlorocarbonate 在 盐酸羟胺 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 为溶剂， 反应 2.5h， 生成 tert-butyl 3-{[((5R)-3-{4-[(E)-amino(hydroxyimino)methyl]phenyl}-4,5-dihydro-5-isoxazolyl)acetyl]amino}-N-((3R)-3-{[tert-butyl(dimethyl)silyl]oxy}butoxycarbonyl)-L-alaninate
  参考文献：
  名称：

  Synthesis of N-Butyl Side Chain Hydroxylated Metabolites of Roxifiban, a Platelet Glycoprotein IIb/IIIa Receptor Antagonist

  摘要：

  Syntheses of three n-butyl side chain hydroxylated metabolites of Roxifiban (5, 6a and 6b) are reported. Initial use of benzyl as hydroxyl protecting group gave poor yield during its removal by catalytic hydrogenation, due to complication from N-O cleavage of the isoxazoline. This problem was eliminated by the use of TBDMS as the hydroxyl protecting group. The chemical structures of these metabolites as well as the intermediates have been fully characterized.

  DOI：

  10.3987/com-04-10087
• 作为产物：
  描述：

  三光气 、 (R)-3-(tert-butyldimethylsilyloxy)-1-butanol 在 三乙胺 作用下， 以 四氢呋喃 为溶剂， 反应 1.5h， 以50%的产率得到(3R)-3-tert-butyl(dimethyl)silyloxybutyl chlorocarbonate
  参考文献：
  名称：

  Synthesis of N-Butyl Side Chain Hydroxylated Metabolites of Roxifiban, a Platelet Glycoprotein IIb/IIIa Receptor Antagonist

  摘要：

  Syntheses of three n-butyl side chain hydroxylated metabolites of Roxifiban (5, 6a and 6b) are reported. Initial use of benzyl as hydroxyl protecting group gave poor yield during its removal by catalytic hydrogenation, due to complication from N-O cleavage of the isoxazoline. This problem was eliminated by the use of TBDMS as the hydroxyl protecting group. The chemical structures of these metabolites as well as the intermediates have been fully characterized.

  DOI：

  10.3987/com-04-10087

文献信息

• Synthesis of N-Butyl Side Chain Hydroxylated Metabolites of Roxifiban, a Platelet Glycoprotein IIb/IIIa Receptor Antagonist
  作者：Jung-Hui Sun、George C. Emmett、Janice L. Hytrek、Jia-Sheng Yan、A. Christine Tabaka-Blom、Christopher A. Teleha

  DOI：10.3987/com-04-10087

  日期：——

  Syntheses of three n-butyl side chain hydroxylated metabolites of Roxifiban (5, 6a and 6b) are reported. Initial use of benzyl as hydroxyl protecting group gave poor yield during its removal by catalytic hydrogenation, due to complication from N-O cleavage of the isoxazoline. This problem was eliminated by the use of TBDMS as the hydroxyl protecting group. The chemical structures of these metabolites as well as the intermediates have been fully characterized.