Abstract
Purpose We found that during TFA-mediated cleavage of azide-containing peptides during solid-phase peptide synthesis a byproduct characterized by a difference of 12 mass units is formed. This study identifies this byproduct, provides a rationale for its formation and a solution for its inhibition. Method NMR and HRMS analyses as well as chemical synthesis is employed to identify the byproduct and probe the mechanism of its formation. Results Data is consistent with the conversion of azide to methylamine which occurs during peptide cleavage likely via a Schmidt rearrangement involving nucleophilic azide attack of t-butyl cations generated during side chain deprotection of Boc- and t-butyl ether groups. Conclusion Installing azide-containing residues using the newly reported 2-(trimethylsilyl)ethoxycarbonyl (Teoc)-protected compound 3a proved effective at significantly thwarting the formation of methyl amine byproduct.