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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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. |
format | Online Article Text |
id | pubmed-7536303 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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