An Alternative Total Synthesis of Pentosidine

作者:Liu Yahua*; Zhang Weihan; Sayre Lawrence M
来源:Journal of Heterocyclic Chemistry, 2011, 48(2): 426-433.
DOI:10.1002/jhet.611

摘要

Pentosidine, a fluorescent advanced glycation endproduct that serves as a biomarker of diabetic complications, kidney dysfunction, oxidative stress, and aging and age-related diseases, was synthesized from 2.3-diaminopyridine and benzyloxycarbonyl (Cbz) protected chiral amino acids N-alpha-Cbz-lysine and N-delta-Cbz-ornithine. Regioselective alkylation of 2-(methylthio)imidazo[4,5-b]pyridine, chlorination of methylthio group, and amination of 2-chloro-imidazo[4,5-b]pyridine are the key steps. Hydantoin protection of amino acids was used and the deprotection under acidic condition was achieved in the presence of glycine.

  • 出版日期2011-3