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dc.contributor.authorWidiyana, Anita P
dc.contributor.authorPutra, Galih S
dc.contributor.authorSulistyowati, Mellany Ika
dc.contributor.authorHardjono, Suko
dc.contributor.authorBudiati, Tutuk
dc.date.accessioned2021-10-11T06:18:27Z
dc.date.available2021-10-11T06:18:27Z
dc.date.issued2017-08-01
dc.identifier.issn0975-7383
dc.identifier.urihttps://www.jocpr.com/abstract/synthesis-method-optimization-of-23disubtitutedquinazolin43hone-derivatives-8955.html
dc.identifier.urihttp://repository.unisma.ac.id/handle/123456789/1920
dc.description[ARCHIVES] Copyright Article from: Journal of Chemical and Pharmaceutical Researchen_US
dc.description.abstractQuinzolinones have various biological activities such as anticancer, antidiabetic, anticonvulsant, antihistaminic, anti inflammatory, antifungal, anthelmintics and antiviral activites. In this research some of compounds 2,3- disubtitutedquinazolin-4(3H)-one derivatives had been synthesized under microwave irradiation. The compounds were obtained from reaction some of benzoxazine derivatives with hydrazine hydrate using microwave irradiation and the result of reaction we obtained 82-96%. The productshad been tested by IR, 1H-NMR, 13C-NMR and Mass Spectroscopy analysis. The using microwave irradiation was more effective and efficient to produce compounds 2,3-disubtituted quinazolin-4(3H)-one derivative because the reaction runs perfectly without any minor products such as compounds N-(2-(hydrazinecarbonyl)phenyl)benzamide derivatives.en_US
dc.language.isoenen_US
dc.publisherJournal of Chemical and Pharmaceutical Research (JOCPR)en_US
dc.relation.ispartofseriesJournal of Chemical and Pharmaceutical Research (JOCPR);Vol.9, Issue 8, Page 24-28
dc.subject2,3-disubtituted quinazolin-4(3H)-one derivativesen_US
dc.subjectN-(2-(hydrazinecarbonyl)phenyl)benzamide derivativesen_US
dc.subjectMicrowave irradiationen_US
dc.titleSynthesis, Method Optimization of 2,3-Disubtitutedquinazolin-4(3H)-Oneen_US
dc.typeArticleen_US


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