(2S)-2-(4-methoxycarbonyl-4-{4-[methyl-(2,2,2-trifluoroacetyl)amino]benzoylamino}butyrylamino)hex-5-enoic acid methyl ester | 1100131-22-3

• 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: (2S)-2-(4-methoxycarbonyl-4-{4-[methyl-(2,2,2-trifluoroacetyl)amino]benzoylamino}butyrylamino)hex-5-enoic acid methyl ester
• CAS: 1100131-22-3
• 化学式: C₂₃H₂₈F₃N₃O₇
• 分子量: 515.486
• InChiKey: YVEZSVHHUVWLOD-IRXDYDNUSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.89
• 重原子数：
  36.0
• 可旋转键数：
  12.0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.43
• 拓扑面积：
  131.11
• 氢给体数：
  2.0
• 氢受体数：
  7.0

反应信息

• 作为反应物：
  描述：

  (2S)-2-(4-methoxycarbonyl-4-{4-[methyl-(2,2,2-trifluoroacetyl)amino]benzoylamino}butyrylamino)hex-5-enoic acid methyl ester 在 二甲基二环氧乙烷 作用下， 以 二氯甲烷 、 丙酮 为溶剂， 反应 2.5h， 以100%的产率得到
  参考文献：
  名称：

  Synthesis of Isopeptide Epoxide Peptidomimetics

  摘要：

  Two epoxide-containing peptidomimetics of the isopeptide, glutatnyl-gamma-glutamate, have been synthesized via a route that should be generally applicable to the synthesis of isopeptide analogues in which an oxirane replaces the scissile peptide bond. Enzymes that catalyze the hydrolysis of peptides and isopeptides are often susceptible to inactivation by electrophilic substrate analogues. In this research, an epoxide was installed as an electrophilic replacement of the scissile isopeptide bond. The C-terminal glutamyl mimic was accessed by the stereospecific synthesis of suitably substituted cyclopentenes, 8 and 10, as surrogates for either the L- or D- enantiomer. The enantiomeric cyclopentenes were further elaborated to incorporate an appended sulfone that was reacted with a suitably protected glutamyl-gamma-semialdehyde in a Julia-Kocienski olefination reaction. This olefination afforded predominantly the desired E-olefin isosteres of L-glutamyl-gamma-D-glutamate and L-glutamyl-gamma-L-glutamate, following which peracid-mediated epoxidation and deprotection provided the epoxide-containing peptidomimetics, 4 and 5.

  DOI：

  10.1021/jo801907p
• 作为产物：
  描述：

  (2S)-2-[4-methoxycarbonyl-4-(4-methylaminobenzoylamino)butyrylamino]hex-5-enoic acid methyl ester 、 三氟乙酸酐 在 三乙胺 作用下， 以 四氢呋喃 、 二氯甲烷 为溶剂， 反应 1.0h， 以84%的产率得到(2S)-2-(4-methoxycarbonyl-4-{4-[methyl-(2,2,2-trifluoroacetyl)amino]benzoylamino}butyrylamino)hex-5-enoic acid methyl ester
  参考文献：
  名称：

  Synthesis of Isopeptide Epoxide Peptidomimetics

  摘要：

  Two epoxide-containing peptidomimetics of the isopeptide, glutatnyl-gamma-glutamate, have been synthesized via a route that should be generally applicable to the synthesis of isopeptide analogues in which an oxirane replaces the scissile peptide bond. Enzymes that catalyze the hydrolysis of peptides and isopeptides are often susceptible to inactivation by electrophilic substrate analogues. In this research, an epoxide was installed as an electrophilic replacement of the scissile isopeptide bond. The C-terminal glutamyl mimic was accessed by the stereospecific synthesis of suitably substituted cyclopentenes, 8 and 10, as surrogates for either the L- or D- enantiomer. The enantiomeric cyclopentenes were further elaborated to incorporate an appended sulfone that was reacted with a suitably protected glutamyl-gamma-semialdehyde in a Julia-Kocienski olefination reaction. This olefination afforded predominantly the desired E-olefin isosteres of L-glutamyl-gamma-D-glutamate and L-glutamyl-gamma-L-glutamate, following which peracid-mediated epoxidation and deprotection provided the epoxide-containing peptidomimetics, 4 and 5.

  DOI：

  10.1021/jo801907p