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Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives
ABSTRACT: New series of Schiff’s bases, hydrazones, thiosemicarbazones, thiazoles, and thiocarbohydrazones of 5-fluoroisatin were synthesized by the reaction of 5-fluoroisatin with primary amines, hydrazine hydrate, and thiocarbohydrazides. Thiosemicarbazones were prepared by reacting hydrazone deri...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Vienna
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087807/ https://www.ncbi.nlm.nih.gov/pubmed/32214479 http://dx.doi.org/10.1007/s00706-013-1034-3 |
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author | Abbas, Samir Y. Farag, Awatef A. Ammar, Yousry A. Atrees, Abeer A. Mohamed, Aly F. El-Henawy, Ahmed A. |
author_facet | Abbas, Samir Y. Farag, Awatef A. Ammar, Yousry A. Atrees, Abeer A. Mohamed, Aly F. El-Henawy, Ahmed A. |
author_sort | Abbas, Samir Y. |
collection | PubMed |
description | ABSTRACT: New series of Schiff’s bases, hydrazones, thiosemicarbazones, thiazoles, and thiocarbohydrazones of 5-fluoroisatin were synthesized by the reaction of 5-fluoroisatin with primary amines, hydrazine hydrate, and thiocarbohydrazides. Thiosemicarbazones were prepared by reacting hydrazone derivatives with isothiocyanates. Upon treatment of thiosemicarbazone derivatives with chloroacetone, the thiazole derivatives were obtained. Some of the prepared compounds exhibited antiviral activity. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-7087807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Springer Vienna |
record_format | MEDLINE/PubMed |
spelling | pubmed-70878072020-03-23 Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives Abbas, Samir Y. Farag, Awatef A. Ammar, Yousry A. Atrees, Abeer A. Mohamed, Aly F. El-Henawy, Ahmed A. Monatsh Chem Original Paper ABSTRACT: New series of Schiff’s bases, hydrazones, thiosemicarbazones, thiazoles, and thiocarbohydrazones of 5-fluoroisatin were synthesized by the reaction of 5-fluoroisatin with primary amines, hydrazine hydrate, and thiocarbohydrazides. Thiosemicarbazones were prepared by reacting hydrazone derivatives with isothiocyanates. Upon treatment of thiosemicarbazone derivatives with chloroacetone, the thiazole derivatives were obtained. Some of the prepared compounds exhibited antiviral activity. GRAPHICAL ABSTRACT: [Image: see text] Springer Vienna 2013-07-12 2013 /pmc/articles/PMC7087807/ /pubmed/32214479 http://dx.doi.org/10.1007/s00706-013-1034-3 Text en © Springer-Verlag Wien 2013 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Paper Abbas, Samir Y. Farag, Awatef A. Ammar, Yousry A. Atrees, Abeer A. Mohamed, Aly F. El-Henawy, Ahmed A. Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
title | Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
title_full | Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
title_fullStr | Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
title_full_unstemmed | Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
title_short | Synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
title_sort | synthesis, characterization, and antiviral activity of novel fluorinated isatin derivatives |
topic | Original Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087807/ https://www.ncbi.nlm.nih.gov/pubmed/32214479 http://dx.doi.org/10.1007/s00706-013-1034-3 |
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