(1S,2R,3S,4R)-3-{(S)-2-[(S)-1-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carbonyl}-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid | 203053-84-3

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (1S,2R,3S,4R)-3-{(S)-2-[(S)-1-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carbonyl}-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid
• 英文别名: (1S,2R,3S,4R)-3-[(2S)-2-[[(2S)-1-[[(2S)-1-methoxy-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]carbamoyl]pyrrolidine-1-carbonyl]bicyclo[2.2.1]hept-5-ene-2-carboxylic acid
• CAS: 203053-84-3
• 化学式: C₃₃H₃₇N₃O₇
• 分子量: 587.673
• InChiKey: XKLUPHYTEWKCEC-PCBADCMMSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.4
• 重原子数：
  43
• 可旋转键数：
  12
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.42
• 拓扑面积：
  142
• 氢给体数：
  3
• 氢受体数：
  7

反应信息

• 作为反应物：
  描述：

  (S)-3-Methyl-2-{(S)-2-[((S)-pyrrolidine-2-carbonyl)-amino]-propionylamino}-butyric acid methyl ester; compound with trifluoro-acetic acid 、 (1S,2R,3S,4R)-3-{(S)-2-[(S)-1-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carbonyl}-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid 在 N-羟基丁二酰亚胺 、 三乙胺 、 N,N'-二环己基碳二亚胺 作用下， 生成 methyl (2S)-2-[[(2S)-2-[[(2S)-1-[(1S,2R,3S,4R)-3-[(2S)-2-[[(2S)-1-[[(2S)-1-methoxy-1-oxo-3-phenylpropan-2-yl]amino]-1-oxo-3-phenylpropan-2-yl]carbamoyl]pyrrolidine-1-carbonyl]bicyclo[2.2.1]hept-5-ene-2-carbonyl]pyrrolidine-2-carbonyl]amino]propanoyl]amino]-3-methylbutanoate
  参考文献：
  名称：

  Synthesis of Peptides and Pseudopeptides Incorporating an endo-(2S,3R)-Norborn-5-ene Residue as a Turn Inducer

  摘要：

  The desymmetrization of endo-norborn-5-ene-2,3-dicarboxylic anhydride (5) by proline derivatives is used to prepare peptides and pseudopeptides incorporating an endo-(2S,3R)-2-amino-3-carboxynorborn-5-ene (1) residue. The peptides contain a single conformationally constrained beta-amino acid residue, while the pseudopeptides also contain a urea linkage and two peptide chains running in parallel directions. The key step in the synthesis is a Curtius rearrangement on the amido acids 6a,b to generate an isocyanate that is then directly reacted with suitably protected amino acids and peptides to give the peptides and pseudopeptides. The synthesis of the peptide analogue 4 is also described; in this compound, the two peptide chains run parallel to one another, and the stereochemistry of the norbornene unit within compound 4 was determined by X-ray analysis of the related peptide analogue 23.

  DOI：

  10.1021/jo9717651
• 作为产物：
  描述：

  TFA·Pro-Phe-Phe-OMe 、 3,6-endomethylene-1,2,3,6-tetrahydrophthalic anhydride 在 三乙胺 作用下， 以 二氯甲烷 为溶剂， 反应 24.0h， 以31%的产率得到(1S,2R,3S,4R)-3-{(S)-2-[(S)-1-((S)-1-Methoxycarbonyl-2-phenyl-ethylcarbamoyl)-2-phenyl-ethylcarbamoyl]-pyrrolidine-1-carbonyl}-bicyclo[2.2.1]hept-5-ene-2-carboxylic acid
  参考文献：
  名称：

  Synthesis of Peptides and Pseudopeptides Incorporating an endo-(2S,3R)-Norborn-5-ene Residue as a Turn Inducer

  摘要：

  The desymmetrization of endo-norborn-5-ene-2,3-dicarboxylic anhydride (5) by proline derivatives is used to prepare peptides and pseudopeptides incorporating an endo-(2S,3R)-2-amino-3-carboxynorborn-5-ene (1) residue. The peptides contain a single conformationally constrained beta-amino acid residue, while the pseudopeptides also contain a urea linkage and two peptide chains running in parallel directions. The key step in the synthesis is a Curtius rearrangement on the amido acids 6a,b to generate an isocyanate that is then directly reacted with suitably protected amino acids and peptides to give the peptides and pseudopeptides. The synthesis of the peptide analogue 4 is also described; in this compound, the two peptide chains run parallel to one another, and the stereochemistry of the norbornene unit within compound 4 was determined by X-ray analysis of the related peptide analogue 23.

  DOI：

  10.1021/jo9717651