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One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives

A variety of bis-heterocycles such as bis(pyrimido[4,5-b]quinolone), bis(chromeno[3′,4':5,6]pyrido[2,3-d]pyrimidine), bis(pyrido[2,3-d:6,5-d']dipyrimidine), and bis(benzo[g]pyrimido[4,5-b]quinolone) derivatives were synthesized via one-pot, multi-component reaction of various 6-aminouracil...

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Detalles Bibliográficos
Autores principales: Masoumi, Milad, Bayat, Mohammad, Hosseini, Fahimeh Sadat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536303/
https://www.ncbi.nlm.nih.gov/pubmed/33033771
http://dx.doi.org/10.1016/j.heliyon.2020.e05047
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author Masoumi, Milad
Bayat, Mohammad
Hosseini, Fahimeh Sadat
author_facet Masoumi, Milad
Bayat, Mohammad
Hosseini, Fahimeh Sadat
author_sort Masoumi, Milad
collection PubMed
description A variety of bis-heterocycles such as bis(pyrimido[4,5-b]quinolone), bis(chromeno[3′,4':5,6]pyrido[2,3-d]pyrimidine), bis(pyrido[2,3-d:6,5-d']dipyrimidine), and bis(benzo[g]pyrimido[4,5-b]quinolone) derivatives were synthesized via one-pot, multi-component reaction of various 6-aminouracils or 6-aminothiouracils, terephthalaldehyde, and CH-acids such as 4-hydroxycoumarin, dimedone, 2-hydroxy-1,4-naphthoquinone, barbituric acid, and thiobarbituric acid in EtOH as a solvent at reflux. The mild conditions, fast rate of reaction, absence of catalyst, different functional group compatibility, simple operation and work-up involving no chromatographic process, are worth mentioning.
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spelling pubmed-75363032020-10-07 One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives Masoumi, Milad Bayat, Mohammad Hosseini, Fahimeh Sadat Heliyon Research Article A variety of bis-heterocycles such as bis(pyrimido[4,5-b]quinolone), bis(chromeno[3′,4':5,6]pyrido[2,3-d]pyrimidine), bis(pyrido[2,3-d:6,5-d']dipyrimidine), and bis(benzo[g]pyrimido[4,5-b]quinolone) derivatives were synthesized via one-pot, multi-component reaction of various 6-aminouracils or 6-aminothiouracils, terephthalaldehyde, and CH-acids such as 4-hydroxycoumarin, dimedone, 2-hydroxy-1,4-naphthoquinone, barbituric acid, and thiobarbituric acid in EtOH as a solvent at reflux. The mild conditions, fast rate of reaction, absence of catalyst, different functional group compatibility, simple operation and work-up involving no chromatographic process, are worth mentioning. Elsevier 2020-10-01 /pmc/articles/PMC7536303/ /pubmed/33033771 http://dx.doi.org/10.1016/j.heliyon.2020.e05047 Text en Crown Copyright © 2020 Published by Elsevier Ltd. http://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
Masoumi, Milad
Bayat, Mohammad
Hosseini, Fahimeh Sadat
One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
title One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
title_full One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
title_fullStr One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
title_full_unstemmed One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
title_short One-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
title_sort one-pot multi-component synthesis of new bis-pyridopyrimidine and bis-pyrimidoquinolone derivatives
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7536303/
https://www.ncbi.nlm.nih.gov/pubmed/33033771
http://dx.doi.org/10.1016/j.heliyon.2020.e05047
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