Synthesis and Antimicrobial Properties of New 4‐(Alkylidene/arylidene)‐amino‐5‐(2‐furanyl)‐2,4‐dihydro‐3 H ‐1,2,4‐triazole‐3‐thiones and 6‐Aryl‐3‐(2‐furanyl)‐7 H ‐1,2,4‐triazolo[3,4‐ b ][1,3,4]thiadiazines

A series of 4‐(alkylidene/arylidene)amino‐5‐(2‐furanyl)‐2,4‐dihydro‐3 H ‐1,2,4‐triazole‐3‐thiones ( 2 ) and 6‐aryl‐3‐(2‐furanyl)‐7 H ‐1,2,4‐triazolo[3,4‐ b ][1,3,4] thiadiazines ( 3 ) were synthesized. The configuration of 2g was assigned on the basis of 1 H‐NMR data. Of the new derivatives tested,...

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Veröffentlicht in:Archiv der Pharmazie (Weinheim) 1996-01, Vol.329 (8-9), p.427-430
Hauptverfasser: Ergenç, Nedime, Ulusoy, Nuray, Çapan, Gültaze, Sanis, Gülten Ötük, Kiraz, Muammer
Format: Artikel
Sprache:eng
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Zusammenfassung:A series of 4‐(alkylidene/arylidene)amino‐5‐(2‐furanyl)‐2,4‐dihydro‐3 H ‐1,2,4‐triazole‐3‐thiones ( 2 ) and 6‐aryl‐3‐(2‐furanyl)‐7 H ‐1,2,4‐triazolo[3,4‐ b ][1,3,4] thiadiazines ( 3 ) were synthesized. The configuration of 2g was assigned on the basis of 1 H‐NMR data. Of the new derivatives tested, only 2b, 2g , and 4f were found to be active against Staphylococcus aureus and/or Staphylococcus epidermidis (MIC 125–1.95 μg/ml), whereas all exhibited varying degrees of antifungal activity (MIC 25–0.8 μg/ml).
ISSN:0365-6233
1521-4184
DOI:10.1002/ardp.19963290811