Publication:
Synthesis and antituberculosis activity of 2-(aryl/alkylamino)-5-(4- aminophenyl)-1,3,4-thiadiazoles and their Schiff bases

dc.contributor.authorsSolak N., Rollas S.
dc.date.accessioned2022-03-28T14:53:32Z
dc.date.accessioned2026-01-11T13:25:51Z
dc.date.available2022-03-28T14:53:32Z
dc.date.issued2006
dc.description.abstractA series of new Schiff bases were synthesized through the condensation reaction of 1,3,4-thiadiazoles containing a aromatic primary amine and 3-hydroxybenzaldehyde, salicylaldehyde, 5-nitrofurfuraldehyde or 3-nitrobenzaldehyde. The synthesized compounds screened for antituberculosis activity against Mycobacterium tuberculosis H37Rv using BACTEC 460 radiometric system. Among the tested compounds, 2-phenylamino-5-[4-(2- hydroxybenzylideneamino)phenyl]-1,3,4-thiadiazol (5a) showed the highest inhibitory activity (51%). The activities of the synthesized Schiff bases were compared with those of the starting 2-(aryl/alkylamino)-5-(4-aminophenyl)-1,3,4- thiadiazoles (4a-e). Some Schiff bases showed higher growth inhibition than the starting amines. ©ARKAT.
dc.identifier.issn14246376
dc.identifier.urihttps://hdl.handle.net/11424/256019
dc.language.isoeng
dc.relation.ispartofArkivoc
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subject1,3,4-thiadiazoles
dc.subjectAntituberculosis activity
dc.subjectSchiff bases
dc.subjectSynthesis
dc.titleSynthesis and antituberculosis activity of 2-(aryl/alkylamino)-5-(4- aminophenyl)-1,3,4-thiadiazoles and their Schiff bases
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage181
oaire.citation.issue12
oaire.citation.startPage173
oaire.citation.titleArkivoc
oaire.citation.volume2006

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