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Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity

We present in this paper a direct and efficient study regarding synthesis and spectral characterization of three series of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety, with potential antimicrobial activity, by using ultrasound (US) irradiation and conventional methods (CV). The synt...

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Autores principales: Diaconu, Dumitrela, Mangalagiu, Violeta, Dunca, Simona, Amariucai-Mantu, Dorina, Antoci, Vasilichia, Roman, Tiberiu, Mangalagiu, Ionel I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660482/
https://www.ncbi.nlm.nih.gov/pubmed/38027984
http://dx.doi.org/10.1016/j.heliyon.2023.e21518
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author Diaconu, Dumitrela
Mangalagiu, Violeta
Dunca, Simona
Amariucai-Mantu, Dorina
Antoci, Vasilichia
Roman, Tiberiu
Mangalagiu, Ionel I.
author_facet Diaconu, Dumitrela
Mangalagiu, Violeta
Dunca, Simona
Amariucai-Mantu, Dorina
Antoci, Vasilichia
Roman, Tiberiu
Mangalagiu, Ionel I.
author_sort Diaconu, Dumitrela
collection PubMed
description We present in this paper a direct and efficient study regarding synthesis and spectral characterization of three series of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety, with potential antimicrobial activity, by using ultrasound (US) irradiation and conventional methods (CV). The synthesis pathway is efficient and direct, in two steps: an initial N-acylation of 8-aminoquinoline followed by metal complexation with variously M(2+) metals (Cd(2+), Co(2+), Cu(2+), Ni(2+), Pd(2+), Zn(2+)). For both type of reactions, N-acylation and complexation, under US irradiations the synthesis have some undeniable advantages: the most relevant being the higher yields, a dramatically decrease for reaction time (with about 150 (one hundred fifty) folds for complexation) comparative with conventional methods (CV) (therefore the spent energy decrease in the same way), a decrease of the amount of used solvents. Taking into account the above considerations these reactions setup could be appreciated as eco-friendly. The structures of the obtained hybrid quinoline – sulfonamide complexes (HQBSM) were determined by elemental analysis and by using spectral investigations: FT-IR, NMR experiments, and X-ray diffraction (in three cases). The FT-IR and NMR spectra of complexes show a similar spectroscopic pattern for all complexes and fully confirm the proposed structures. The X-ray spectra analyses prove without doubts the structure of metal complexes, indicating that their structure depends essentially by two factors: the nature of metal and the nature of sulfonamide-quinoline moieties. Complexes containing 4-methoxy-benzoyl moiety and Zn(2+) (e.g. 6a) are tetra-coordinated while in the Ni(2+) complex (e.g. 6e) the metallic ion forms a distorted square-based bi-pyramid. In the complexes containing 4-nitro-benzoyl moiety and Cd(2+) (e.g. 5d) the metallic ion forms a triangular bipyramid. The antibacterial and antifungal assay reveal that only hybrid HQBSM complex (4e) (with 4-chlorophenyl moiety and Ni(2+) in molecule) have a significant antibacterial activity.
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spelling pubmed-106604822023-11-03 Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity Diaconu, Dumitrela Mangalagiu, Violeta Dunca, Simona Amariucai-Mantu, Dorina Antoci, Vasilichia Roman, Tiberiu Mangalagiu, Ionel I. Heliyon Research Article We present in this paper a direct and efficient study regarding synthesis and spectral characterization of three series of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety, with potential antimicrobial activity, by using ultrasound (US) irradiation and conventional methods (CV). The synthesis pathway is efficient and direct, in two steps: an initial N-acylation of 8-aminoquinoline followed by metal complexation with variously M(2+) metals (Cd(2+), Co(2+), Cu(2+), Ni(2+), Pd(2+), Zn(2+)). For both type of reactions, N-acylation and complexation, under US irradiations the synthesis have some undeniable advantages: the most relevant being the higher yields, a dramatically decrease for reaction time (with about 150 (one hundred fifty) folds for complexation) comparative with conventional methods (CV) (therefore the spent energy decrease in the same way), a decrease of the amount of used solvents. Taking into account the above considerations these reactions setup could be appreciated as eco-friendly. The structures of the obtained hybrid quinoline – sulfonamide complexes (HQBSM) were determined by elemental analysis and by using spectral investigations: FT-IR, NMR experiments, and X-ray diffraction (in three cases). The FT-IR and NMR spectra of complexes show a similar spectroscopic pattern for all complexes and fully confirm the proposed structures. The X-ray spectra analyses prove without doubts the structure of metal complexes, indicating that their structure depends essentially by two factors: the nature of metal and the nature of sulfonamide-quinoline moieties. Complexes containing 4-methoxy-benzoyl moiety and Zn(2+) (e.g. 6a) are tetra-coordinated while in the Ni(2+) complex (e.g. 6e) the metallic ion forms a distorted square-based bi-pyramid. In the complexes containing 4-nitro-benzoyl moiety and Cd(2+) (e.g. 5d) the metallic ion forms a triangular bipyramid. The antibacterial and antifungal assay reveal that only hybrid HQBSM complex (4e) (with 4-chlorophenyl moiety and Ni(2+) in molecule) have a significant antibacterial activity. Elsevier 2023-11-03 /pmc/articles/PMC10660482/ /pubmed/38027984 http://dx.doi.org/10.1016/j.heliyon.2023.e21518 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Diaconu, Dumitrela
Mangalagiu, Violeta
Dunca, Simona
Amariucai-Mantu, Dorina
Antoci, Vasilichia
Roman, Tiberiu
Mangalagiu, Ionel I.
Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity
title Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity
title_full Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity
title_fullStr Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity
title_full_unstemmed Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity
title_short Ultrasound assisted synthesis of hybrid quinoline anchored with 4-R-benzenesulfonamide moiety with potential antimicrobial activity
title_sort ultrasound assisted synthesis of hybrid quinoline anchored with 4-r-benzenesulfonamide moiety with potential antimicrobial activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660482/
https://www.ncbi.nlm.nih.gov/pubmed/38027984
http://dx.doi.org/10.1016/j.heliyon.2023.e21518
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