Rapid and Mild Synthesis of Amino Acid N-Carboxy Anhydrides: Basic-to-Acidic Flash Switching in a Microflow Reactor

被引:58
|
作者
Otake, Yuma [1 ,2 ]
Nakamura, Hiroyuki [1 ]
Fuse, Shinichiro [1 ]
机构
[1] Tokyo Inst Technol, Lab Chem & Life Sci, Inst Innovat Res, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
[2] Tokyo Inst Technol, Sch Life Sci & Technol, Midori Ku, 4259 Nagatsuta Cho, Yokohama, Kanagawa 2268503, Japan
基金
日本学术振兴会;
关键词
acylation; amino acids; anhydrides; flow chemistry; peptides; AMIDE BOND FORMATION; EPOXIDATION REACTION; CARBOXYANHYDRIDE; CHEMISTRY; POLYMERIZATION; POLYPEPTIDES; CYCLIZATION; ACTIVATION; PROLINE; PEPTIDE;
D O I
10.1002/anie.201803549
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Polymerization of N-carboxy anhydrides (NCAs) is the primary process used to prepare polypeptides. The synthesis of various pure NCAs is key to the efficient synthesis of polypeptides. The only practical method that can be used to synthesize NCAs requires harsh acidic conditions that make acid-labile substrates unusable and results in an undesired ring opening of NCAs. Basic-to-acidic flash switching and subsequent flash dilution technology in a microflow reactor was used to demonstrate the synthesis of NCAs. It is both rapid (0.1s) and mild (20 degrees C) and includes substrates containing acid-labile functional groups. The basic-to-acidic flash switching enabled both an acceleration of the desired NCA formation and avoided the undesired ring opening of NCAs. The flash dilution precluded the undesired decomposition of acid-labile functional groups. The developed process allowed the synthesis of various NCAs which cannot be readily synthesized using conventional batch methods.
引用
收藏
页码:11389 / 11393
页数:5
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