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Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst

[Image: see text] DABCO was used as a basic and inexpensive catalyst for the synthesis of some new benzyloxy pyrimido[4,5-b]quinoline derivatives and 1,2,3- triazole-fused pyrimido[4,5-b]quinolines by the one-pot multi-component reaction of various benzyloxy benzaldehydes or benzylic −1,2,3-triazol-...

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Autores principales: Esmaili, Soheila, Moosavi-Zare, Ahmad Reza, Khazaei, Ardeshir, Najafi, Zahra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2022
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753531/
https://www.ncbi.nlm.nih.gov/pubmed/36530277
http://dx.doi.org/10.1021/acsomega.2c05896
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author Esmaili, Soheila
Moosavi-Zare, Ahmad Reza
Khazaei, Ardeshir
Najafi, Zahra
author_facet Esmaili, Soheila
Moosavi-Zare, Ahmad Reza
Khazaei, Ardeshir
Najafi, Zahra
author_sort Esmaili, Soheila
collection PubMed
description [Image: see text] DABCO was used as a basic and inexpensive catalyst for the synthesis of some new benzyloxy pyrimido[4,5-b]quinoline derivatives and 1,2,3- triazole-fused pyrimido[4,5-b]quinolines by the one-pot multi-component reaction of various benzyloxy benzaldehydes or benzylic −1,2,3-triazol-4-yl-methoxy benzaldehydes with dimedone and 6-amino-1,3-dimethyluracil at 90 °C under the solvent-free condition.
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spelling pubmed-97535312022-12-16 Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst Esmaili, Soheila Moosavi-Zare, Ahmad Reza Khazaei, Ardeshir Najafi, Zahra ACS Omega [Image: see text] DABCO was used as a basic and inexpensive catalyst for the synthesis of some new benzyloxy pyrimido[4,5-b]quinoline derivatives and 1,2,3- triazole-fused pyrimido[4,5-b]quinolines by the one-pot multi-component reaction of various benzyloxy benzaldehydes or benzylic −1,2,3-triazol-4-yl-methoxy benzaldehydes with dimedone and 6-amino-1,3-dimethyluracil at 90 °C under the solvent-free condition. American Chemical Society 2022-12-02 /pmc/articles/PMC9753531/ /pubmed/36530277 http://dx.doi.org/10.1021/acsomega.2c05896 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Esmaili, Soheila
Moosavi-Zare, Ahmad Reza
Khazaei, Ardeshir
Najafi, Zahra
Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst
title Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst
title_full Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst
title_fullStr Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst
title_full_unstemmed Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst
title_short Synthesis of Novel Pyrimido[4,5-b] Quinolines Containing Benzyloxy and 1,2,3-Triazole Moieties by DABCO as a Basic Catalyst
title_sort synthesis of novel pyrimido[4,5-b] quinolines containing benzyloxy and 1,2,3-triazole moieties by dabco as a basic catalyst
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9753531/
https://www.ncbi.nlm.nih.gov/pubmed/36530277
http://dx.doi.org/10.1021/acsomega.2c05896
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