Ribose conversion with amino acids into pyrraline platform chemicals – expeditious synthesis of diverse pyrrole-fused alkaloid compounds. Issue 50 (23rd September 2021)

• Record Type: Journal Article
• Authors: Cho, Soohyeon; Gu, Lina; IN, Ik Joon; Wu, Bo; Lee, Taehoon; Kim, Hakwon; Koo, Sangho
• Is Part Of: RSC advances. Volume 11:Issue 50(2021)
• Page Start: 31511
• Page End: 31525
• Publication Date: 2021-09-23
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d1ra06110k
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : One-pot conversion of sustainable d -ribose with l -amino acid, methyl esters produced pyrrole-2-carbaldehydes 5 in reasonable yields (32–63%) under pressurized conditions of 2.5 atm at 80 °C. Abstract : One-pot conversion of sustainable d -ribose with l -amino acid, methyl esters produced pyrrole-2-carbaldehydes 5 in reasonable yields (32–63%) under pressurized conditions of 2.5 atm at 80 °C. The value-added pyrraline compounds 5 as platform chemicals were utilized for quick installation of poly-heterocyclic cores for the development of pyrrole-motif natural and artificial therapeutic agents. A pyrrole-fused piperazin-2-one scaffold 6 was prepared by reductive amination of pyrralines 5 with benzylamine. While further cyclization of pyrralines 5 with ethane-1, 2-diamine produced pyrrolo-piperazin-2-ones 7 with an extra imidazolidine ring, the reaction with 2-amino alcohols derived from natural l -amino acids, alanine, valine, and phenylalanine, respectively provided pyrrolo-piperazin-2-ones 8, 9, and 10 with oxazolidine as the third structural core. Cell viability and an anti-inflammatory effect of the synthesized compounds were briefly tested by the MTT method and the Griess assay, among which 8h and 10g exhibited significant anti-inflammatory effects with negligible cell toxicity.