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Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles
The synthesis of the title compounds was achieved using ethyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate (1) as starting material. The reaction of the amino ester 1 with phenylisothiocyanate in boiling ethanol afforded the thiourea derivative 5. The cyclization reactions...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257348/ https://www.ncbi.nlm.nih.gov/pubmed/20428071 http://dx.doi.org/10.3390/molecules15042651 |
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author | El-Kashef, Hussein Farghaly, Abdel-Rahman Al-Hazmi, Ahmed Terme, Thierry Vanelle, Patrice |
author_facet | El-Kashef, Hussein Farghaly, Abdel-Rahman Al-Hazmi, Ahmed Terme, Thierry Vanelle, Patrice |
author_sort | El-Kashef, Hussein |
collection | PubMed |
description | The synthesis of the title compounds was achieved using ethyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate (1) as starting material. The reaction of the amino ester 1 with phenylisothiocyanate in boiling ethanol afforded the thiourea derivative 5. The cyclization reactions of 5 under different reaction conditions led to different pyridothienopyrimidine derivatives. Other reactions of the latter derivatives leading to pyrido[4',3':4,5]thieno[2,3-d]triazolo[1,5-a]pyrimidines are also presented. |
format | Online Article Text |
id | pubmed-6257348 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Molecular Diversity Preservation International |
record_format | MEDLINE/PubMed |
spelling | pubmed-62573482018-11-30 Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles El-Kashef, Hussein Farghaly, Abdel-Rahman Al-Hazmi, Ahmed Terme, Thierry Vanelle, Patrice Molecules Article The synthesis of the title compounds was achieved using ethyl 2-amino-6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine-3-carboxylate (1) as starting material. The reaction of the amino ester 1 with phenylisothiocyanate in boiling ethanol afforded the thiourea derivative 5. The cyclization reactions of 5 under different reaction conditions led to different pyridothienopyrimidine derivatives. Other reactions of the latter derivatives leading to pyrido[4',3':4,5]thieno[2,3-d]triazolo[1,5-a]pyrimidines are also presented. Molecular Diversity Preservation International 2010-04-12 /pmc/articles/PMC6257348/ /pubmed/20428071 http://dx.doi.org/10.3390/molecules15042651 Text en © 2010 by the authors; http://creativecommons.org/licenses/by/3.0/ licensee Molecular Diversity Preservation International, Basel, Switzerland. This article is an open-access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article El-Kashef, Hussein Farghaly, Abdel-Rahman Al-Hazmi, Ahmed Terme, Thierry Vanelle, Patrice Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles |
title | Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles |
title_full | Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles |
title_fullStr | Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles |
title_full_unstemmed | Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles |
title_short | Pyridine-Based Heterocycles. Synthesis of New Pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and Related Heterocycles |
title_sort | pyridine-based heterocycles. synthesis of new pyrido [4',3':4,5]thieno[2,3-d]pyrimidines and related heterocycles |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257348/ https://www.ncbi.nlm.nih.gov/pubmed/20428071 http://dx.doi.org/10.3390/molecules15042651 |
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