N-Halosuccinimides Mediated Deprotection of Cysteine-S Protecting Groups for One-Pot Regioselective Synthesis of Disulfide Bonds in Peptides Under Mild Aqueous Conditions

Abstract

Cysteine (Cys) with side chain protected by groups acetamidomethyl (Acm), 1,3-thiazolidine-4-carbonyl (Thz) and t-butyl (tBu) has been commonly used for the synthesis of correct disulfide bonds in peptides. Deprotection of these protected groups can be achieved by use of metal salts under harshly removal conditions. In this work, N-chlorosuccinimide (NCS) and N-bromosuccinimide (NBS) are demonstrated to deprotect these protecting groups to directly form an intramolecular disulfide bond in peptide. In addition, all the deprotection reactions were complete within 10 min, conferring the fast reaction rates. Moreover, it is also demonstrated that formation of a stable halosulfonium cation plays a critical role in these deprotection reactions. When NCS and NBS were employed for deprotecting these groups, two disulfide bonds in α-conotoxin SI, α-conotoxin IMI and apamin were synthesized regioselectively by an one-pot approach, rendering satisfied yields.

Keywords: N-halosuccinimides, multiple disulfide bonds, peptides, one-pot synthesis, deprotection