Phosphosulfonic acid-catalyzed green synthesis and bioassay of α-aryl-α′-1,3,4-thiadiazolyl aminophosphonates

A series of new α‐aminophosphonates containing 1,3,4‐thiadiazole moiety (4a–l) were synthesized via a simple, efficient, and one‐pot three‐component Kabachnik–Fields reaction of 2‐amino‐5‐ethyl‐1,3,4‐thiadiazole with various aryl/heteroaryl aldehydes and diethylphosphite under solvent‐free microwave...

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Veröffentlicht in:Heteroatom chemistry 2016-09, Vol.27 (5), p.269-278
Hauptverfasser: Gundluru, Mohan, Sarva, Santhisudha, Kandula, Madhu Kumar Reddy, Netala, Vasudeva Reddy, Tartte, Vijaya, Cirandur, Suresh Reddy
Format: Artikel
Sprache:eng
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Zusammenfassung:A series of new α‐aminophosphonates containing 1,3,4‐thiadiazole moiety (4a–l) were synthesized via a simple, efficient, and one‐pot three‐component Kabachnik–Fields reaction of 2‐amino‐5‐ethyl‐1,3,4‐thiadiazole with various aryl/heteroaryl aldehydes and diethylphosphite under solvent‐free microwave irradiation conditions using phosphosulfonic acid, as a reusable and heterogeneous solid acid catalyst. All the title compounds were screened for radical scavenging activity by DPPH and H2O2 methods, and antimicrobial activity against bacteria (Gram‐positive and Gram‐negative) and fungi using the disc diffusion technique. They exhibited potent in vitro antioxidant and moderate antimicrobial activity.
ISSN:1042-7163
1098-1071
DOI:10.1002/hc.21325