Synthesis and biological evaluation of some 1,3,4-oxadiazole derivatives

The acid hydrazides ( 2) derived from ibuprofen and 4-methylthiophenyl acetic acids have been subjected to cyclization with carbon disulphide under basic conditions to yield 1,3,4-oxadiazol-2-thiones ( 3) which on aminomethylation with formaldehyde and secondary amines afforded a series of Mannich b...

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Veröffentlicht in:European journal of medicinal chemistry 2010-11, Vol.45 (11), p.5225-5233
Hauptverfasser: Manjunatha, K., Poojary, Boja, Lobo, Prajwal L., Fernandes, Jennifer, Kumari, N. Suchetha
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Sprache:eng
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Zusammenfassung:The acid hydrazides ( 2) derived from ibuprofen and 4-methylthiophenyl acetic acids have been subjected to cyclization with carbon disulphide under basic conditions to yield 1,3,4-oxadiazol-2-thiones ( 3) which on aminomethylation with formaldehyde and secondary amines afforded a series of Mannich bases ( 4 and 5). Purity of the compounds has been confirmed by TLC. Structures of these compounds were established on the basis of elemental analyses and spectral studies. The newly synthesized compounds were evaluated for their anti-inflammatory, analgesic, ulcerogenic and antimicrobial activities. A series of oxadiazole derived Mannich bases were synthesized and evaluated for their antimicrobial and anti-inflammatory activities. [Display omitted]
ISSN:0223-5234
1768-3254
DOI:10.1016/j.ejmech.2010.08.039