(S)-2-tert-Butoxycarbonylamino-2-[(2S,5'S,5''S)-5',5''-diisobutyl-2-isopropyl-3,4',4''-trioxo-5''-(2-oxo-ethyl)-2,3,4',5',4'',5''-hexahydro-1H,1'H,1''H-[2,3';5',3'']terpyrrol-4-yl]-3-phenyl-propionic acid methyl ester | 159216-06-5

• 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: (S)-2-tert-Butoxycarbonylamino-2-[(2S,5'S,5''S)-5',5''-diisobutyl-2-isopropyl-3,4',4''-trioxo-5''-(2-oxo-ethyl)-2,3,4',5',4'',5''-hexahydro-1H,1'H,1''H-[2,3';5',3'']terpyrrol-4-yl]-3-phenyl-propionic acid methyl ester
• 英文别名: methyl (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-2-[(5S)-5-[(5S)-5-(2-methylpropyl)-5-[(5S)-5-(2-methylpropyl)-4-oxo-5-(2-oxoethyl)-1H-pyrrol-3-yl]-4-oxo-1H-pyrrol-3-yl]-4-oxo-5-propan-2-yl-1H-pyrrol-3-yl]-3-phenylpropanoate
• CAS: 159216-06-5
• 化学式: C₄₀H₅₄N₄O₈
• 分子量: 718.891
• InChiKey: KJHSCHQJGIOBFG-BSUMSBOOSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  6.4
• 重原子数：
  52
• 可旋转键数：
  17
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.55
• 拓扑面积：
  169
• 氢给体数：
  4
• 氢受体数：
  11

反应信息

• 作为反应物：
  描述：

  (S)-2-tert-Butoxycarbonylamino-2-[(2S,5'S,5''S)-5',5''-diisobutyl-2-isopropyl-3,4',4''-trioxo-5''-(2-oxo-ethyl)-2,3,4',5',4'',5''-hexahydro-1H,1'H,1''H-[2,3';5',3'']terpyrrol-4-yl]-3-phenyl-propionic acid methyl ester 在 sodium periodate 、 四氧化锇 、 双(三甲基硅烷基)氨基钾 作用下， 以 四氢呋喃 、 氯仿 、 水 、 丙酮 、 甲苯 、 苯 为溶剂， 反应 26.75h， 生成
  参考文献：
  名称：

  De Novo Design, Synthesis, and X-ray Crystal Structures of Pyrrolinone-Based .beta.-Strand Peptidomimetics

  摘要：

  The de novo design and synthesis of a novel non-peptide scaffolding for beta-strand/sheet mimics are described. The scaffold consists of repeating 3,5,5-trisubstituted pyrrolinone (enaminone) units punctuated with appropriate amino acid side chains. The iterative construction of the pyrrolinones exploits a highly efficient cyclization of metalloimines, the latter derived from C-terminal aldehydes and readily available alpha-substituted alpha-amino ester building blocks. As predicted by interactive computer modeling and confirmed by X-ray crystallography, the polypyrrolinones present the side chains and carbonyl hydrogen-bond accepters in a solid-state conformation which mimics polypeptide beta-sheets. Importantly, the enaminone NH protons form hydrogen bonds both intramolecularly, stabilizing the beta-strand conformation, and intermolecularly, promoting sheet formation. The presence or absence of the nitrogen protecting group controlled antiparallel versus parallel sheet formation.

  DOI：

  10.1021/ja00101a017
• 作为产物：
  描述：

  (R)-2-Amino-2-benzyl-5-methyl-hex-4-enoic acid methyl ester 在 sodium periodate 、 四氧化锇 、 双(三甲基硅烷基)氨基钾 、 臭氧 、 N-甲基吗啉氧化物 、 三苯基膦 作用下， 以 四氢呋喃 、 氯仿 、 水 、 丙酮 、 甲苯 为溶剂， 反应 92.09h， 生成 (S)-2-tert-Butoxycarbonylamino-2-[(2S,5'S,5''S)-5',5''-diisobutyl-2-isopropyl-3,4',4''-trioxo-5''-(2-oxo-ethyl)-2,3,4',5',4'',5''-hexahydro-1H,1'H,1''H-[2,3';5',3'']terpyrrol-4-yl]-3-phenyl-propionic acid methyl ester
  参考文献：
  名称：

  De Novo Design, Synthesis, and X-ray Crystal Structures of Pyrrolinone-Based .beta.-Strand Peptidomimetics

  摘要：

  The de novo design and synthesis of a novel non-peptide scaffolding for beta-strand/sheet mimics are described. The scaffold consists of repeating 3,5,5-trisubstituted pyrrolinone (enaminone) units punctuated with appropriate amino acid side chains. The iterative construction of the pyrrolinones exploits a highly efficient cyclization of metalloimines, the latter derived from C-terminal aldehydes and readily available alpha-substituted alpha-amino ester building blocks. As predicted by interactive computer modeling and confirmed by X-ray crystallography, the polypyrrolinones present the side chains and carbonyl hydrogen-bond accepters in a solid-state conformation which mimics polypeptide beta-sheets. Importantly, the enaminone NH protons form hydrogen bonds both intramolecularly, stabilizing the beta-strand conformation, and intermolecularly, promoting sheet formation. The presence or absence of the nitrogen protecting group controlled antiparallel versus parallel sheet formation.

  DOI：

  10.1021/ja00101a017

文献信息

• A Second-Generation Synthesis of Polypyrrolinone Nonpeptidomimetics:  Prelude to the Synthesis of Polypyrrolinones on Solid Support
  作者：Amos B. Smith、Hu Liu、Ralph Hirschmann

  DOI：10.1021/ol0059293

  日期：2000.7.1

  [reaction: see text] A second-generation asymmetric synthesis of polypyrrolinones (3) has been achieved exploiting scalemic alpha-aminolactones (1) as building blocks. Imine formation between an appropriate lactone (1) and aldehyde (2), followed in turn by pyrrolinone ring construction promoted by KHMDS in the presence of 18-crown-6 and modified Swern oxidation furnished pyrrolinone aldehyde 3. This iterative

  [反应：见正文]利用垢型α-氨基内酯（1）作为结构单元，已经实现了第二代不对称合成的聚吡咯烷酮（3）。在适当的内酯（1）和醛（2）之间形成亚胺，然后依次在18-crown-6和修饰的Swern氧化作用下，由KHMDS促进吡咯烷酮环的构建，从而得到吡咯烷酮醛3。这种迭代，有效的三步法该方案为在固体载体上合成聚吡咯烷酮铺平了道路。