Please use this identifier to cite or link to this item: http://148.72.244.84:8080/xmlui/handle/xmlui/5042
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dc.contributor.authorKhalid Mahmod Daoud-
dc.contributor.authorMohanad Yakdhan Saleh-
dc.contributor.authorShaima Samer Ismael-
dc.date.accessioned2023-10-19T08:19:44Z-
dc.date.available2023-10-19T08:19:44Z-
dc.date.issued2017-
dc.identifier.citationhttp://dx.doi.org/10.24237/djps.1303.201Cen_US
dc.identifier.issn2222-8373-
dc.identifier.urihttp://148.72.244.84:8080/xmlui/handle/xmlui/5042-
dc.description.abstractIn this paper demonstrated the synthesis of some fused 1,2,4-triazoles derivatives ; Terphthalic acid condensated with ethanol to obtain diethyl terephthalate (1) in the presence of sulfuric acid as catalyst., the ethyl ester (1) was mixed with hydrazine hydrate is ethyl alcohol to give terephthalohydrazide (2). The hydrazide derivative (2) then reacted with ammonium thiocyanate to give yield 2,2'-terephthaloylbis(hydrazinecarbothioamide) (3). 3,4- diamine-bis – 1,2,4-triazole derivative (4) was obtained by reaction of a compound (3) with hydrazine hydrate. 5,5'-(1,4-phenylene)bis(4H-1,2,4-triazole-3,4-diamine) (4) was reacted with a proper aldehyde to yield Schiff bases derivatives (5,6,7).1-(1H-[1,2,4]triazolo[4,3-b][1,2,4]triazol-5-yl)-4-(3H-[1,2,4]triazolo[4,3-b][1,2,4]triazol-6-yl) benzene derivatives (8,9,10) were yielded by reaction a Schiff bases derivative with glacial acetic acid. The structures of the synthesized compounds were confirmed by physical and spectral methods.en_US
dc.description.sponsorshiphttps://djps.uodiyala.edu.iq/en_US
dc.language.isoenen_US
dc.publisheruniversity of Diyalaen_US
dc.subjectHeterocyclic compounds, 1, 2, 4-trazole, fused ring, terephthalic acid.en_US
dc.titleSynthesis and Biological Active of Some Substituted 1,2,4-Triazoles and Their Fused Ring Derivativesen_US
dc.typeArticleen_US
Appears in Collections:مجلة ديالى للعلوم الاكاديمية / Academic Science Journal (Acad. Sci. J.)

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