methyl (S)-2-((S)-2-acetyl-2'-oxo-2,4-dihydro-1H-spiro[isoquinoline-3,3'-pyrrolidin]-1'-yl)propanoate | 1191929-78-8

• 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: methyl (S)-2-((S)-2-acetyl-2'-oxo-2,4-dihydro-1H-spiro[isoquinoline-3,3'-pyrrolidin]-1'-yl)propanoate
• 英文别名: methyl (2S)-2-[(3S)-2-acetyl-2'-oxospiro[1,4-dihydroisoquinoline-3,3'-pyrrolidine]-1'-yl]propanoate
• CAS: 1191929-78-8
• 化学式: C₁₈H₂₂N₂O₄
• 分子量: 330.384
• InChiKey: NHUMDIWPLMRMGB-KPZWWZAWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.1
• 重原子数：
  24
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  66.9
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  methyl (S)-2-((S)-2-acetyl-2'-oxo-2,4-dihydro-1H-spiro[isoquinoline-3,3'-pyrrolidin]-1'-yl)propanoate 、 甲胺 以 乙醇 为溶剂， 反应 12.0h， 以90%的产率得到(S)-2-((S)-2-acetyl-2'-oxo-2,4-dihydro-1H-spiro[isoquinoline-3,3'-pyrrolidin]-1'-yl)-N-methylpropanamide
  参考文献：
  名称：

  Tetrahydroisoquinoline-Based Spirocyclic Lactam as a Type II′ β-Turn Inducing Peptide Mimetic

  摘要：

  We present here spirocyclic lactam derivatives, embodying D-Phe and L-Ala amino acids as the central core and acting as tetrapeptide and hexapeptide mimetics. An efficient route for their synthesis is demonstrated by using the strategic combination of Seebach's self-reproduction of chirality chemistry and the Pictet-Spengler condensation as key steps. The conformational behavior of peptide mimetics was Investigated by Molecular modeling, X-ray crystallography, NMR (solvent and temperature dependence), IR spectroscopy, and circular dichroism. All data suggest very stable and highly predictable type II' beta-turn conformations.

  DOI：

  10.1021/jo901480d
• 作为产物：
  描述：

  methyl (S)-2-((S)-2'-oxo-2,4-dihydro-1H-spiro[isoquinoline-3,3'-pyrrolidin]-1'-yl)propanoate 、 乙酸酐 在 N,N-二异丙基乙胺 作用下， 以 二氯甲烷 为溶剂， 以98%的产率得到methyl (S)-2-((S)-2-acetyl-2'-oxo-2,4-dihydro-1H-spiro[isoquinoline-3,3'-pyrrolidin]-1'-yl)propanoate
  参考文献：
  名称：

  Tetrahydroisoquinoline-Based Spirocyclic Lactam as a Type II′ β-Turn Inducing Peptide Mimetic

  摘要：

  We present here spirocyclic lactam derivatives, embodying D-Phe and L-Ala amino acids as the central core and acting as tetrapeptide and hexapeptide mimetics. An efficient route for their synthesis is demonstrated by using the strategic combination of Seebach's self-reproduction of chirality chemistry and the Pictet-Spengler condensation as key steps. The conformational behavior of peptide mimetics was Investigated by Molecular modeling, X-ray crystallography, NMR (solvent and temperature dependence), IR spectroscopy, and circular dichroism. All data suggest very stable and highly predictable type II' beta-turn conformations.

  DOI：

  10.1021/jo901480d

文献信息

• Tetrahydroisoquinoline-Based Spirocyclic Lactam as a Type II′ β-Turn Inducing Peptide Mimetic
  作者：Giordano Lesma、Nicola Landoni、Tullio Pilati、Alessandro Sacchetti、Alessandra Silvani

  DOI：10.1021/jo901480d

  日期：2009.11.6

  We present here spirocyclic lactam derivatives, embodying D-Phe and L-Ala amino acids as the central core and acting as tetrapeptide and hexapeptide mimetics. An efficient route for their synthesis is demonstrated by using the strategic combination of Seebach's self-reproduction of chirality chemistry and the Pictet-Spengler condensation as key steps. The conformational behavior of peptide mimetics was Investigated by Molecular modeling, X-ray crystallography, NMR (solvent and temperature dependence), IR spectroscopy, and circular dichroism. All data suggest very stable and highly predictable type II' beta-turn conformations.