Please use this identifier to cite or link to this item: http://148.72.244.84/xmlui/handle/xmlui/6348
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dc.contributor.authorAhlam J. Zaier*-
dc.date.accessioned2023-10-23T07:56:24Z-
dc.date.available2023-10-23T07:56:24Z-
dc.date.issued2016-
dc.identifier.issn2222-8373-
dc.identifier.urihttp://148.72.244.84:8080/xmlui/handle/xmlui/6348-
dc.description.abstractA stable Schiff bases were prepared by condensation reaction between equimolar quantities of aromatic aldehydes with aromatic amines. Aromatic Schiff bases were undergo nucleophilic addition with acetyl chloride to give N-(chloro(phenyl)methyl)-N phenylacetamides. The reaction of latter with diethylmalonate in basic medium yeild diethyl 2-(phenyl(N-phenylacetamido)methyl)malonates. The latter condense with urea in basic medium to give derivatives of barbiturate which used in the medical field as hypnotics. The prepared compounds were identified by FT.IR and UV-Vis spectroscopy.en_US
dc.description.sponsorshiphttps://djps.uodiyala.edu.iq/en_US
dc.language.isoenen_US
dc.publisherUniversity of Diyalaen_US
dc.subjectKey words: Schiff base, Acetamide, Barbiturate, Pyrimidineen_US
dc.titleSynthesis of Some New Barbiturate Derivatives Via Schiff Basesen_US
dc.title.alternativeتحضير بعض مشتقات الباربيتيورات الجديدة عن طريق قواعد شيفen_US
dc.typeArticleen_US
Appears in Collections:مجلة ديالى للعلوم الاكاديمية / Academic Science Journal (Acad. Sci. J.)

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