Microwave-Assisted and Solvent-Free Synthesis of Quinoline Derivatives and Their Fluorescence Properties
- 1 January 2021
- journal article
- research article
- Published by The Japan Institute of Heterocyclic Chemistry in HETEROCYCLES
- Vol. 102 (4), 647-658
- https://doi.org/10.3987/com-20-14384
Abstract
A protocol for the microwave-assisted Friedlander synthesis of quinoline derivatives under solvent-free conditions has been developed. According to this modified method, quinoline derivatives were synthesized by condensation of 2-aminobenzophenone with the corresponding carbonyl compounds in the presence of phosphomolybdic acid for 8 min in a 320 W microwave with yields ranging from 61% to 90%. The fluorescence properties of the synthesized compounds were studied, and all compounds showed good fluorescence properties. The substituted groups and the concentrations of quinolines and solvents had significant effects on the compounds' fluorescence properties. This method provides a convenient way to obtain quinolines, and is beneficial to the application of these compounds.Keywords
This publication has 49 references indexed in Scilit:
- Synthesis, crystal structure and spectroscopic study of novel benzimidazoles and benzimidazo[1,2-a]quinolines as potential chemosensors for different cationsDyes and Pigments, 2012
- Polycyclic Quinolones (Part 1) — Thieno[2,3-b]benzo[h]quinoline Derivatives: Design, Synthesis, Preliminary in vitro and in silico StudiesHETEROCYCLES, 2012
- Microwave-assisted synthesis of quinoline, isoquinoline, quinoxaline and quinazoline derivatives as CB2 receptor agonistsBioorganic & Medicinal Chemistry, 2011
- New quinoline derivatives: Synthesis and investigation of antibacterial and antituberculosis propertiesEuropean Journal of Medicinal Chemistry, 2010
- Cerium(IV) Ammonium Nitrate Is an Excellent, General Catalyst for the Friedländer and Friedländer−Borsche Quinoline Syntheses: Very Efficient Access to the Antitumor Alkaloid Luotonin AThe Journal of Organic Chemistry, 2009
- Search for new pharmacophores for antimalarial activity. Part I: Synthesis and antimalarial activity of new 2-methyl-6-ureido-4-quinolinamidesBioorganic & Medicinal Chemistry, 2009
- Transition-Metal-Free Indirect Friedländer Synthesis of Quinolines from AlcoholsThe Journal of Organic Chemistry, 2008
- Synthesis, cytotoxicity, and anti-inflammatory evaluation of 2-(furan-2-yl)-4-(phenoxy)quinoline derivatives. Part 4Bioorganic & Medicinal Chemistry, 2006
- Molecular iodine: a highly efficient catalyst in the synthesis of quinolinesvia Friedländer annulationOrganic & Biomolecular Chemistry, 2005
- Ionic Liquid-Promoted Regiospecific Friedlander Annulation: Novel Synthesis of Quinolines and Fused Polycyclic QuinolinesThe Journal of Organic Chemistry, 2003