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The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds
New coumarin derivatives, namely 7-[(5-amino-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one (4), 5-[(2-oxo-2H-chromen-7-yloxy)methyl]-1,3,4-thiadiazol-2(3H)-one (5), 2-[2-(2-oxo-2H-chromen-7-yloxy)acetyl]-N-phenylhydrazinecarbothioamide (7), 7-[(5-(phenylamino)-1,3,4-thiadiazol-2-yl)methoxy]-2H-chr...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264737/ https://www.ncbi.nlm.nih.gov/pubmed/21832973 http://dx.doi.org/10.3390/molecules16086833 |
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author | Al-Amiery, Ahmed A. Musa, Ahmed Y. Kadhum, Abdul Amir H. Mohamad, Abu Bakar |
author_facet | Al-Amiery, Ahmed A. Musa, Ahmed Y. Kadhum, Abdul Amir H. Mohamad, Abu Bakar |
author_sort | Al-Amiery, Ahmed A. |
collection | PubMed |
description | New coumarin derivatives, namely 7-[(5-amino-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one (4), 5-[(2-oxo-2H-chromen-7-yloxy)methyl]-1,3,4-thiadiazol-2(3H)-one (5), 2-[2-(2-oxo-2H-chromen-7-yloxy)acetyl]-N-phenylhydrazinecarbothioamide (7), 7-[(5-(phenylamino)-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one (8) and 7-[(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)methoxy]-2H-chromen-2-one (9) were prepared starting from the natural compound umbelliferone (1). The newly synthesized compounds were characterized by elemental analysis and spectral studies (IR, (1)H-NMR and (13)C-NMR). |
format | Online Article Text |
id | pubmed-6264737 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62647372018-12-10 The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds Al-Amiery, Ahmed A. Musa, Ahmed Y. Kadhum, Abdul Amir H. Mohamad, Abu Bakar Molecules Article New coumarin derivatives, namely 7-[(5-amino-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one (4), 5-[(2-oxo-2H-chromen-7-yloxy)methyl]-1,3,4-thiadiazol-2(3H)-one (5), 2-[2-(2-oxo-2H-chromen-7-yloxy)acetyl]-N-phenylhydrazinecarbothioamide (7), 7-[(5-(phenylamino)-1,3,4-thiadiazol-2-yl)methoxy]-2H-chromen-2-one (8) and 7-[(5-mercapto-4-phenyl-4H-1,2,4-triazol-3-yl)methoxy]-2H-chromen-2-one (9) were prepared starting from the natural compound umbelliferone (1). The newly synthesized compounds were characterized by elemental analysis and spectral studies (IR, (1)H-NMR and (13)C-NMR). MDPI 2011-08-10 /pmc/articles/PMC6264737/ /pubmed/21832973 http://dx.doi.org/10.3390/molecules16086833 Text en © 2011 by the authors; licensee MDPI, 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 Al-Amiery, Ahmed A. Musa, Ahmed Y. Kadhum, Abdul Amir H. Mohamad, Abu Bakar The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds |
title | The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds |
title_full | The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds |
title_fullStr | The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds |
title_full_unstemmed | The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds |
title_short | The Use of Umbelliferone in the Synthesis of New Heterocyclic Compounds |
title_sort | use of umbelliferone in the synthesis of new heterocyclic compounds |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264737/ https://www.ncbi.nlm.nih.gov/pubmed/21832973 http://dx.doi.org/10.3390/molecules16086833 |
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