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Synthesis of 4‐(5‐Amino‐1,3,4‐thiadiazol‐2‐yl)pyrrolidin‐2‐ones and Their Antifungal Activity Научная публикация

Журнал ChemistrySelect
ISSN: 2365-6549
Вых. Данные Год: 2025, Том: 10, Номер: 36, Номер статьи : e03719, Страниц : DOI: 10.1002/slct.202503719
Авторы Serkov Sergei A. 1 , Sigay Natalya V. 1 , Kostikova Natalya N. 1 , Alekseenko Anna L. 2 , Kolotyrkina Natalya G. 1 , Popkov Sergey V. 2 , Gazieva Galina A. 1
Организации
1 N. D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences 47 Leninsky Prosp. Moscow 119991 Russian Federation
2 Faculty of Chemical‐Pharmaceutical Technologies and Biomedical Preparations D. I. Mendeleev University of Chemical Technology of Russia 9 Miusskaya Sq. Moscow 125047 Russian Federation

Реферат: A novel series of 1-aryl- and 1-alkyl-4-(5-amino-1,3,4-thiadiazol-2-yl)pyrrolidin-2-ones was synthesized by the condensation of 1-aryl- or 1-alkyl-5-oxopyrrolidine-3-carboxylic acids and thiosemicarbazide upon heating with concentrated sulfuric acid and characterized using IR, 1H NMR, 13C NMR, and HRMS spectral data. The proposed approach was suitable for the synthesis of some 4-(5-amino-1,3,4-thiadiazol-2-yl)-1-heteroarylpyrrolidin-2-ones. The protocol ensures the stability of the pyrrolidinone cycle under reaction conditions. The synthesized compounds showed significant antifungal activity against phytopathogens R. solani and V. inaequalis. Two the most active compounds, 4-(5-amino-1,3,4-thiadiazol-2-yl)-1-(4-chlorobenzyl)pyrrolidin-2-one and 4-(5-amino-1,3,4-thiadiazol-2-yl)-1-(6-nitrobenzothiazol-2-yl)pyrrolidin-2-one, also showed moderate activity against B. sorokiniana. They inhibited the mycelial growth of R.solani, V. inaequalis and B. sorokiniana by 100, 60-78, and 53-55%, respectively, which is higher than that of the reference compound triadimefon (43%, 41%, and 44%, respectively).
Библиографическая ссылка: Serkov S.A. , Sigay N.V. , Kostikova N.N. , Alekseenko A.L. , Kolotyrkina N.G. , Popkov S.V. , Gazieva G.A.
Synthesis of 4‐(5‐Amino‐1,3,4‐thiadiazol‐2‐yl)pyrrolidin‐2‐ones and Their Antifungal Activity
ChemistrySelect. 2025. V.10. N36. e03719 . DOI: 10.1002/slct.202503719 WOS Scopus OpenAlex
Идентификаторы БД:
≡ Web of science: WOS:001576612700001
≡ Scopus: 2-s2.0-105016800221
≡ OpenAlex: W4414408222
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