tert-butyl (2S,2'R,1''S)-2-[2-(1-benzyloxycarbonylamino-2-methylpropyl)-5-oxopyrrolidin-1-yl]-4-methylpentanoate | 1242316-72-8

• 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: tert-butyl (2S,2'R,1''S)-2-[2-(1-benzyloxycarbonylamino-2-methylpropyl)-5-oxopyrrolidin-1-yl]-4-methylpentanoate
• 英文别名: tert-butyl (2S)-4-methyl-2-[(2R)-2-[(1S)-2-methyl-1-(phenylmethoxycarbonylamino)propyl]-5-oxopyrrolidin-1-yl]pentanoate
• CAS: 1242316-72-8
• 化学式: C₂₆H₄₀N₂O₅
• 分子量: 460.614
• InChiKey: IYXVLDWOAGJGQC-GIWBLDEGSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  33
• 可旋转键数：
  12
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.65
• 拓扑面积：
  84.9
• 氢给体数：
  1
• 氢受体数：
  5

反应信息

• 作为反应物：
  描述：

  tert-butyl (2S,2'R,1''S)-2-[2-(1-benzyloxycarbonylamino-2-methylpropyl)-5-oxopyrrolidin-1-yl]-4-methylpentanoate 在 三氟乙酸 作用下， 以 水 为溶剂， 生成
  参考文献：
  名称：

  γ-Lactam-containing peptidomimetics

  摘要：

  Protected diaminoalcohols obtained through allyl addition to alpha-amino acid-derived imines and subsequent hydroboration were used for the preparation of pyrrolidinones and pyrrolidines. Pyrrolidinones were synthesized with moderate yields by oxidation of the hydroxy function with tetrapropylammonium perruthenate/N-methylmorpholine-N-oxide and concomitant cyclization while pyrrolidines were synthesized in good yields by tosylation of the hydroxy group and subsequent intramolecular nucleophilic substitution. Thus accessible substrates were transferred into peptidomimetics by attachment of amino acid moieties at both termini using conventional peptide coupling strategies. Molecular mechanics optimizations suggest that these substrates preferentially adopt a turn conformation. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.05.099
• 作为产物：
  描述：

  tert-butyl (2S,2'S)-2-(1-benzyloxycarbonylamino-2-isopropyl-6-oxopiperidin-3-ylamino)-4-methylpentanoate 反应 2191.5h， 生成 tert-butyl (2S,2'R,1''S)-2-[2-(1-benzyloxycarbonylamino-2-methylpropyl)-5-oxopyrrolidin-1-yl]-4-methylpentanoate
  参考文献：
  名称：

  γ-Lactam-containing peptidomimetics

  摘要：

  Protected diaminoalcohols obtained through allyl addition to alpha-amino acid-derived imines and subsequent hydroboration were used for the preparation of pyrrolidinones and pyrrolidines. Pyrrolidinones were synthesized with moderate yields by oxidation of the hydroxy function with tetrapropylammonium perruthenate/N-methylmorpholine-N-oxide and concomitant cyclization while pyrrolidines were synthesized in good yields by tosylation of the hydroxy group and subsequent intramolecular nucleophilic substitution. Thus accessible substrates were transferred into peptidomimetics by attachment of amino acid moieties at both termini using conventional peptide coupling strategies. Molecular mechanics optimizations suggest that these substrates preferentially adopt a turn conformation. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2010.05.099