An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols

A practical and convenient method for the synthesis of pyridine-3-thiols using substituted 3-iodopyridines as starting compounds has been developed. Based on the use of thiobenzoic acid as a sulfur donor in a two-step procedure, this approach made it possible to synthesize a number of pyridine-3-thi...

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Main Authors: Oleksandr V. Borysov, Dmytro P. Bohdan
Format: Article
Language:English
Published: National University of Pharmacy (Kharkiv) 2025-04-01
Series:Журнал органічної та фармацевтичної хімії
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Online Access:https://ophcj.nuph.edu.ua/article/view/324523
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author Oleksandr V. Borysov
Dmytro P. Bohdan
author_facet Oleksandr V. Borysov
Dmytro P. Bohdan
author_sort Oleksandr V. Borysov
collection DOAJ
description A practical and convenient method for the synthesis of pyridine-3-thiols using substituted 3-iodopyridines as starting compounds has been developed. Based on the use of thiobenzoic acid as a sulfur donor in a two-step procedure, this approach made it possible to synthesize a number of pyridine-3-thiols with F, Cl, Br, CH3, OCH3 substituents at various positions of the pyridine ring. The procedure presented gives high yields of the target products with a purity of 95% and is suitable for synthesis in tens of grams.
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record_format Article
series Журнал органічної та фармацевтичної хімії
spelling doaj-art-c36df18c7fc64dfc9cf80739089e71d32025-08-20T03:29:24ZengNational University of Pharmacy (Kharkiv)Журнал органічної та фармацевтичної хімії2308-83032518-15482025-04-01231434810.24959/ophcj.25.324523An Efficient Synthesis of a Variety of Substituted Pyridine-3-ThiolsOleksandr V. Borysov0https://orcid.org/0000-0003-0360-9295Dmytro P. Bohdan1Institute of Organic Chemistry of the National Academy of Sciences of Ukraine; Enamine Ltd., UkraineInstitute of Organic Chemistry of the National Academy of Sciences of Ukraine, UkraineA practical and convenient method for the synthesis of pyridine-3-thiols using substituted 3-iodopyridines as starting compounds has been developed. Based on the use of thiobenzoic acid as a sulfur donor in a two-step procedure, this approach made it possible to synthesize a number of pyridine-3-thiols with F, Cl, Br, CH3, OCH3 substituents at various positions of the pyridine ring. The procedure presented gives high yields of the target products with a purity of 95% and is suitable for synthesis in tens of grams.https://ophcj.nuph.edu.ua/article/view/324523pyridinethiolsthiobenzoic acidchromatographyhydrolysis
spellingShingle Oleksandr V. Borysov
Dmytro P. Bohdan
An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols
Журнал органічної та фармацевтичної хімії
pyridine
thiols
thiobenzoic acid
chromatography
hydrolysis
title An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols
title_full An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols
title_fullStr An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols
title_full_unstemmed An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols
title_short An Efficient Synthesis of a Variety of Substituted Pyridine-3-Thiols
title_sort efficient synthesis of a variety of substituted pyridine 3 thiols
topic pyridine
thiols
thiobenzoic acid
chromatography
hydrolysis
url https://ophcj.nuph.edu.ua/article/view/324523
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