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Novel Brönsted Acidic Ionic Liquids Confined in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions
[Image: see text] The effective and simple one-pot, three-component protocol for the synthesis of dihydropyrido[2,3-d]pyrimidine derivatives is presented using a triethylenediamine or imidazole Brönsted acidic, ionic-liquid-supported Zr metal–organic framework (TEDA/IMIZ-BAIL@UiO-66) as a green, nov...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648245/ https://www.ncbi.nlm.nih.gov/pubmed/31460153 http://dx.doi.org/10.1021/acsomega.9b00178 |
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author | Mirhosseini-Eshkevari, Boshra Esnaashari, Manzarbanoo Ghasemzadeh, Mohammad Ali |
author_facet | Mirhosseini-Eshkevari, Boshra Esnaashari, Manzarbanoo Ghasemzadeh, Mohammad Ali |
author_sort | Mirhosseini-Eshkevari, Boshra |
collection | PubMed |
description | [Image: see text] The effective and simple one-pot, three-component protocol for the synthesis of dihydropyrido[2,3-d]pyrimidine derivatives is presented using a triethylenediamine or imidazole Brönsted acidic, ionic-liquid-supported Zr metal–organic framework (TEDA/IMIZ-BAIL@UiO-66) as a green, novel, and retrievable heterogeneous catalyst under mild conditions. The multicomponent reactions of 6-amino-1,3-dimethyl uracil, various aromatic aldehydes, and acetyl acetone were conducted under solvent-free conditions so that dihydropyrido[2,3-d]pyrimidine derivatives can be obtained. It is possible to separate and purify the respective products easily using crystallization. We can recycle the catalysts six times without losing any major activity. Also, the characterization of the catalyst was done by energy-dispersive X-ray, field emission scanning electron microscopy, Fourier transform infrared, Brunauer–Emmett–Teller, X-ray diffraction, and thermogravimetric analysis analyses. |
format | Online Article Text |
id | pubmed-6648245 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66482452019-08-27 Novel Brönsted Acidic Ionic Liquids Confined in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions Mirhosseini-Eshkevari, Boshra Esnaashari, Manzarbanoo Ghasemzadeh, Mohammad Ali ACS Omega [Image: see text] The effective and simple one-pot, three-component protocol for the synthesis of dihydropyrido[2,3-d]pyrimidine derivatives is presented using a triethylenediamine or imidazole Brönsted acidic, ionic-liquid-supported Zr metal–organic framework (TEDA/IMIZ-BAIL@UiO-66) as a green, novel, and retrievable heterogeneous catalyst under mild conditions. The multicomponent reactions of 6-amino-1,3-dimethyl uracil, various aromatic aldehydes, and acetyl acetone were conducted under solvent-free conditions so that dihydropyrido[2,3-d]pyrimidine derivatives can be obtained. It is possible to separate and purify the respective products easily using crystallization. We can recycle the catalysts six times without losing any major activity. Also, the characterization of the catalyst was done by energy-dispersive X-ray, field emission scanning electron microscopy, Fourier transform infrared, Brunauer–Emmett–Teller, X-ray diffraction, and thermogravimetric analysis analyses. American Chemical Society 2019-06-18 /pmc/articles/PMC6648245/ /pubmed/31460153 http://dx.doi.org/10.1021/acsomega.9b00178 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Mirhosseini-Eshkevari, Boshra Esnaashari, Manzarbanoo Ghasemzadeh, Mohammad Ali Novel Brönsted Acidic Ionic Liquids Confined in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions |
title | Novel Brönsted Acidic Ionic Liquids Confined
in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions |
title_full | Novel Brönsted Acidic Ionic Liquids Confined
in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions |
title_fullStr | Novel Brönsted Acidic Ionic Liquids Confined
in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions |
title_full_unstemmed | Novel Brönsted Acidic Ionic Liquids Confined
in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions |
title_short | Novel Brönsted Acidic Ionic Liquids Confined
in UiO-66 Nanocages for the Synthesis of Dihydropyrido[2,3-d]Pyrimidine Derivatives under Solvent-Free Conditions |
title_sort | novel brönsted acidic ionic liquids confined
in uio-66 nanocages for the synthesis of dihydropyrido[2,3-d]pyrimidine derivatives under solvent-free conditions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648245/ https://www.ncbi.nlm.nih.gov/pubmed/31460153 http://dx.doi.org/10.1021/acsomega.9b00178 |
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