Synthesis of 5-azolyl-2,4-dihydro-3H-1,2,4-triazole-3-thiones and 5-azolyl-1,3,4-thiadiazol-2-amines based on derivatives of 5-arylisoxazole-3-carboxylic and 4,5-dichloroisothiazole-3-carboxylic acids

[Figure not available: see fulltext.] 2-Mercapto-1,3,4-triazoles and 2-amino-1,3,4-thiadiazoles were synthesized by successive transformations of 5-arylisoxazole- and 4,5-dichloroisothiazole-3-carboxylic acids and their derivatives. The amino group of 5-(4,5-dichloroisothiazol-3-yl)-1,3,4-thiadiazol-2-amine was acylated with 5-phenylisoxazole-3-carboxylic acid chloride. Simple approaches to the preparation of previously unknown heterocyclic assemblies containing two or three azole rings with a high potential for biological activity are described. © 2021, Springer Science+Business Media, LLC, part of Springer Nature.

Авторы
Petkevich S.K.1 , Zhukovskaya N.А.1 , Dikusar E.А.1 , Akishina E.А.1 , Kurman P.V.2 , Nikitina E.V. 3 , Zaytsev V.P. 3 , Potkin V.I.1
Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
5
Язык
Английский
Страницы
594-598
Статус
Опубликовано
Том
57
Год
2021
Организации
  • 1 Institute of Physical Organic Chemistry, National Academy of Sciences of Belarus, 13 Surganova St, Minsk, 220072, Belarus
  • 2 Institute of Bioorganic Chemistry, National Academy of Sciences of Belarus, 5/2 Akademika V. F. Kuprevicha St, Minsk, 220141, Belarus
  • 3 RUDN University, 6 Miklukho-Maklaya St, Moscow, 117198, Russian Federation
Ключевые слова
heterocyclization; isothiazole; isoxazole; thiadiazoles; thiosemicarbazides; triazoles
Дата создания
20.07.2021
Дата изменения
20.07.2021
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/74296/
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