methyl (2S)-3-(4-methoxyphenyl)-2-[methyl(phenylmethoxycarbonyl)amino]propanoate | 192211-84-0

• 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 (2S)-3-(4-methoxyphenyl)-2-[methyl(phenylmethoxycarbonyl)amino]propanoate
• CAS: 192211-84-0
• 化学式: C₂₀H₂₃NO₅
• 分子量: 357.406
• InChiKey: QFFJUFJTMHMQHQ-SFHVURJKSA-N

物化性质

• 沸点：
  489.4±45.0 °C(Predicted)
• 密度：
  1.175±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.5
• 重原子数：
  26
• 可旋转键数：
  9
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.3
• 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：

  methyl (2S)-3-(4-methoxyphenyl)-2-[methyl(phenylmethoxycarbonyl)amino]propanoate 在 palladium on activated charcoal lithium hydroxide 、 氢气 、 三乙胺 作用下， 以 四氢呋喃 、 甲醇 、 二氯甲烷 、 乙酸乙酯 为溶剂， 反应 21.0h， 生成 (2S)-2-[acetyl(methyl)amino]-3-(4-methoxyphenyl)propanoic acid
  参考文献：
  名称：

  Synthesis of a Reduced Ring Analog of Didemnin B

  摘要：

  As part of investigations directed toward the determination of the essential/nonessential structural features for the bioactivities of didemnin B, we designed a reduced ring analog in which three moieties, namely the tyrosine side chain, the isostatine hydroxyl, and the side chain (L-lactyl-L-prolyl-N-Me-D-leucine), were in their presumed bioactive conformation. In designing the reduced ring analog, we eliminated the leucine-proline portion of the macrocycle core and replaced if with an n-butyl linker in order to elucidate its role. According to MM2 calculations (MacroModel molecular modeling), this analog was of lower energy than the natural product didemnin B, and both structures were superimposable. The synthetic strategy involved four disconnections. Macrocyclization was accomplished at the activated carboxylic acid of the alpha-(alpha-hydroxyisovaleryl)-propionyl unit (HIP) and the protected amine of the n-butyl linker using a modification of Schmidt's protocol. After selective deprotection of the hydroxyl and amino groups of the macrocycle, the peptide side chain was introduced using (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) as the activating reagent.

  DOI：

  10.1021/jo9623696
• 作为产物：
  描述：

  氯甲酸苄酯 在 四丁基硫酸氢铵 、 sodium carbonate 、 potassium hydroxide 作用下， 以 氯仿 、 水 为溶剂， 生成 methyl (2S)-3-(4-methoxyphenyl)-2-[methyl(phenylmethoxycarbonyl)amino]propanoate
  参考文献：
  名称：

  Synthesis of O-Me Ulongamide B and O-Me Ulongamide C, Natural Modified Cyclodepsipeptides

  摘要：

  Synthesis of O-Me ulongamide B and O-Me ulongamide C, modified natural cyclodepsipeptides, was achieved by a convergent route. The respective dipeptides and tridepsipeptides were coupled, obtaining linear depsipentapeptides, which were then deprotected and cyclized. These compounds were tested against three different types of human carcinoma cells and showed only moderate activity.

  DOI：

  10.1080/00397911.2011.618284

文献信息

• Synthetic studies of didemnins. IV. Synthesis of the macrocycle
  作者：William R. Ewing、Bruce D. Harris、Wen-Ren Li、Madeleine M. Joullie

  DOI：10.1016/s0040-4039(01)80647-x

  日期：1989.1

  A stereocontrolled route to the 23-membered macrocycle found in the didemnins is described.

  描述了在双氢精蛋白中发现的到23元大环的立体控制途径。
• Syntheses of Acyclic Analogs of Didemnin B
  作者：Joshi M. Ramanjulu、Madeleine M. Joullié、Wen-Ren Li

  DOI：10.1080/00397919708004186

  日期：1997.9

  Abstract The syntheses of three modified peptide fragments of the cyclodepsipeptide didemnin B are reported. The HIP and isostatine (1st) units of the didemnin B macrocycle were simplified to a Z-alanine residue and the ester linkage (through threonine of the tetrapeptide) was replaced with amide linkages through the amines of glycine, D-alanine and an ethylenediamine linker. The latter permitted the

  摘要 报道了环缩肽didemnin B的三个修饰肽片段的合成。didemnin B 大环的 HIP 和异抑制素（第一）单元被简化为 Z-丙氨酸残基，酯键（通过四肽的苏氨酸）通过甘氨酸、D-丙氨酸和乙二胺接头的胺被酰胺键取代. 后者允许连接 N-Me-D-Leu-Pro-Lac 部分以分别提供类似物 2、3 和 4。
• Synthesis of <i>O</i>-Me Ulongamide B and <i>O</i>-Me Ulongamide C, Natural Modified Cyclodepsipeptides
  作者：Cuauhtémoc Alvarado、Gerardo Hernández、Eduardo Díaz、José D. Soano、Miguel A. Vilchis-Reyes、Miguel A. Martínez-Urbina、Angel Guzmán

  DOI：10.1080/00397911.2011.618284

  日期：2013.3.1

  Synthesis of O-Me ulongamide B and O-Me ulongamide C, modified natural cyclodepsipeptides, was achieved by a convergent route. The respective dipeptides and tridepsipeptides were coupled, obtaining linear depsipentapeptides, which were then deprotected and cyclized. These compounds were tested against three different types of human carcinoma cells and showed only moderate activity.
• Synthesis of a Reduced Ring Analog of Didemnin B
  作者：Joshi M. Ramanjulu、Xiaobin Ding、Madeleine M. Joullié、Wen-Ren Li

  DOI：10.1021/jo9623696

  日期：1997.7.1

  As part of investigations directed toward the determination of the essential/nonessential structural features for the bioactivities of didemnin B, we designed a reduced ring analog in which three moieties, namely the tyrosine side chain, the isostatine hydroxyl, and the side chain (L-lactyl-L-prolyl-N-Me-D-leucine), were in their presumed bioactive conformation. In designing the reduced ring analog, we eliminated the leucine-proline portion of the macrocycle core and replaced if with an n-butyl linker in order to elucidate its role. According to MM2 calculations (MacroModel molecular modeling), this analog was of lower energy than the natural product didemnin B, and both structures were superimposable. The synthetic strategy involved four disconnections. Macrocyclization was accomplished at the activated carboxylic acid of the alpha-(alpha-hydroxyisovaleryl)-propionyl unit (HIP) and the protected amine of the n-butyl linker using a modification of Schmidt's protocol. After selective deprotection of the hydroxyl and amino groups of the macrocycle, the peptide side chain was introduced using (benzotriazol-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate (BOP) as the activating reagent.