(9H-fluoren-9-yl)methyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)ethylcarbamate | 1161880-97-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 芴
• 英文名称: (9H-fluoren-9-yl)methyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)ethylcarbamate
• 英文别名: 9H-fluoren-9-ylmethyl N-[(2S)-1-[2-(2-bromo-3,5-dinitrophenyl)ethylamino]-1-oxopropan-2-yl]carbamate
• CAS: 1161880-97-2
• 化学式: C₂₆H₂₃BrN₄O₇
• 分子量: 583.395
• InChiKey: FSJSNTUGXVKQHU-HNNXBMFYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.1
• 重原子数：
  38
• 可旋转键数：
  8
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.23
• 拓扑面积：
  159
• 氢给体数：
  2
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  2-(2-溴-3,5-二硝基苯基)乙胺盐酸盐 、 Fmoc-L-丙氨酸 在 N-甲基吗啉 、 氯甲酸异丁酯 、 三乙胺 作用下， 以 二氯甲烷 、 N,N-二甲基甲酰胺 为溶剂， 反应 1.0h， 以92%的产率得到(9H-fluoren-9-yl)methyl (S)-1-(2-bromo-3,5-dinitrophenethylcarbamoyl)ethylcarbamate
  参考文献：
  名称：

  Preparation of Photoactivable Amino Acid Derivatives

  摘要：

  A range of N-protected-alpha-amino acyl-5,7-dinitroindolines 3a-z were prepared in good yields from commercially available N-protected-alpha-amino acids 1a-z by a two-step sequence of acylation and intramolecular amide N-arylation. Subsequent photochemical acylation of the N-protected-alpha-amino acyl-5,7-dinitroindolines 3e,g,r afforded the corresponding N-protected-alpha-amino acid amides 22e,g,r (77-92%) under mild conditions. All these reactions occurred with complete retention of chirality as evidenced by NMR analysis. This scheme provides an attractive and alternative method to the conventional acylation of alpha-amino acids, especially in cases where the amide bond needs to be formed without the use of a coupling reagent.

  DOI：

  10.1021/jo900442p

文献信息

• Preparation of Photoactivable Amino Acid Derivatives
  作者：Jean-Luc Débieux、Christian G. Bochet

  DOI：10.1021/jo900442p

  日期：2009.6.19

  A range of N-protected-alpha-amino acyl-5,7-dinitroindolines 3a-z were prepared in good yields from commercially available N-protected-alpha-amino acids 1a-z by a two-step sequence of acylation and intramolecular amide N-arylation. Subsequent photochemical acylation of the N-protected-alpha-amino acyl-5,7-dinitroindolines 3e,g,r afforded the corresponding N-protected-alpha-amino acid amides 22e,g,r (77-92%) under mild conditions. All these reactions occurred with complete retention of chirality as evidenced by NMR analysis. This scheme provides an attractive and alternative method to the conventional acylation of alpha-amino acids, especially in cases where the amide bond needs to be formed without the use of a coupling reagent.