[3-(13)C]-(3S,5S,6R)-4-benzyloxycarbonyl-3-[3'-(tert-butyldimethylsilyloxy)prop-1'-yl]-5,6-diphenylmorpholin-2-one | 1196980-12-7

• 分子结构分类: 有机化合物 - 苯丙烷和聚酮 - 二苯乙烯类
• 英文名称: [3-(13)C]-(3S,5S,6R)-4-benzyloxycarbonyl-3-[3'-(tert-butyldimethylsilyloxy)prop-1'-yl]-5,6-diphenylmorpholin-2-one
• 英文别名: benzyl (3S,5S,6R)-3-[3-[tert-butyl(dimethyl)silyl]oxypropyl]-2-oxo-5,6-diphenyl-(313C)1,4-oxazinane-4-carboxylate
• CAS: 1196980-12-7
• 化学式: C₃₃H₄₁NO₅Si
• 分子量: 560.767
• InChiKey: IEXZWZWWUKTSNE-LVWVUXHNSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.84
• 重原子数：
  40
• 可旋转键数：
  11
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.39
• 拓扑面积：
  65.1
• 氢给体数：
  0
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  [3-(13)C]-(3S,5S,6R)-4-benzyloxycarbonyl-3-[3'-(tert-butyldimethylsilyloxy)prop-1'-yl]-5,6-diphenylmorpholin-2-one 在 potassium hydrogensulfate 、 水 作用下， 以 甲醇 为溶剂， 反应 5.0h， 以78%的产率得到[3-(13)C]-(3S,5S,6R)-4-benzyloxycarbonyl-5,6-diphenyl-3-(3'-hydroxyprop-1'-yl)morpholin-2-one
  参考文献：
  名称：

  Enantioselective Syntheses of α-Fmoc-Pbf-[2-¹³C]-l-arginine and Fmoc-[1,3-¹³C₂]-l-proline and Incorporation into the Neurotensin Receptor 1 Ligand, NT₈₋₁₃

  摘要：

  Enantioselective syntheses of selectively labeled, orthogonally protected [2-C-13]L-arginine and [1,3-C-13(2)]-L-proline are described from the commercially available precursors [2-C-13]bromoacetic acid and potassium [C-13]cyanide, Interestingly the enhanced signal assigned to C-2 in the C-13 NMR spectrum of alpha-Fmoc-Pbf-[2-C-13]-L-arginine was very broad at room temperature. The two Fmoc-labeled amino acids were used to prepare [2-C-13]-Arg9 and [1,3-C-13(2)]-Pro 10 labeled ligand (NT8-13) by manual Fmoc-SPSS.

  DOI：

  10.1021/jo9014497
• 作为产物：
  描述：

  [3-(13)C]-(5S,6R)-4-benzyloxycarbonyl-5,6-diphenylmorpholin-2-one 、 1-碘-3-[(叔-丁基二甲基硅烷基)氧基]丙烷 在 lithium hexamethyldisilazane 作用下， 以 四氢呋喃 、 六甲基磷酰三胺 为溶剂， 反应 6.0h， 以63%的产率得到[3-(13)C]-(3S,5S,6R)-4-benzyloxycarbonyl-3-[3'-(tert-butyldimethylsilyloxy)prop-1'-yl]-5,6-diphenylmorpholin-2-one
  参考文献：
  名称：

  Enantioselective Syntheses of α-Fmoc-Pbf-[2-¹³C]-l-arginine and Fmoc-[1,3-¹³C₂]-l-proline and Incorporation into the Neurotensin Receptor 1 Ligand, NT₈₋₁₃

  摘要：

  Enantioselective syntheses of selectively labeled, orthogonally protected [2-C-13]L-arginine and [1,3-C-13(2)]-L-proline are described from the commercially available precursors [2-C-13]bromoacetic acid and potassium [C-13]cyanide, Interestingly the enhanced signal assigned to C-2 in the C-13 NMR spectrum of alpha-Fmoc-Pbf-[2-C-13]-L-arginine was very broad at room temperature. The two Fmoc-labeled amino acids were used to prepare [2-C-13]-Arg9 and [1,3-C-13(2)]-Pro 10 labeled ligand (NT8-13) by manual Fmoc-SPSS.

  DOI：

  10.1021/jo9014497

文献信息

• Enantioselective Syntheses of α-Fmoc-Pbf-[2-¹³C]-<scp>l</scp>-arginine and Fmoc-[1,3-¹³C₂]-<scp>l</scp>-proline and Incorporation into the Neurotensin Receptor 1 Ligand, NT₈₋₁₃
  作者：Chuanjun Song、Satita Tapaneeyakorn、Annabel C. Murphy、Craig Butts、Anthony Watts、Christine L. Willis

  DOI：10.1021/jo9014497

  日期：2009.12.4

  Enantioselective syntheses of selectively labeled, orthogonally protected [2-C-13]L-arginine and [1,3-C-13(2)]-L-proline are described from the commercially available precursors [2-C-13]bromoacetic acid and potassium [C-13]cyanide, Interestingly the enhanced signal assigned to C-2 in the C-13 NMR spectrum of alpha-Fmoc-Pbf-[2-C-13]-L-arginine was very broad at room temperature. The two Fmoc-labeled amino acids were used to prepare [2-C-13]-Arg9 and [1,3-C-13(2)]-Pro 10 labeled ligand (NT8-13) by manual Fmoc-SPSS.