Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16503
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dc.contributor.authorAbdo, Mohamed A-
dc.contributor.authorZeid, Ibrahim F-
dc.contributor.authorEI-Hiti, Gamal A-
dc.contributor.authorMahmoud, Olfat E-
dc.date.accessioned2013-03-27T19:44:07Z-
dc.date.available2013-03-27T19:44:07Z-
dc.date.issued1999-07-
dc.identifier.urihttp://hdl.handle.net/123456789/16503-
dc.description850-853en_US
dc.description.abstractReaction of 2-phenyl-3, 1-benzoxazin-4H-one 1 with thiocarbohydrazide in refluxing ethanol affords 2-phenyl-3- thiosemicarbazido-4(3H)-quinazolinone 2. However, thioxotetrazinoquinazo line 3 is obtained in 79% isolated yield when the reaction mixture is fused in an oil bath at 160°C. Compound 3 is also obtained when compound 2 is heated in an oil bath at 170°C. On the other hand , compound 3 reacts with paraformaldehyde and secondary amines to afford the corresponding quinazoline derivatives 4 and 5. The diazonium salt of 3-amino-2-phenyl- 4(3H)-quinazolinone 6 reacts with some active methylene compounds (diethyl malonate, ethyl acetoacetate, malononitrile and acetyl acetone) to affords the quinazolinone derivatives 8-11 in good yields. Reactions of 8 with hydrazine hydrate and phenyl hydrazine afford the corresponding pyrazolonoquinazolinones 12 and 13, respectively. Reaction of 8 with urea furnishes pyrimidinoquinazolinones 14 in 79% isolated yield. However, reaction of 11 with hydrazine hydrate gives pyrazoloquinazolinones 15 in 83% isolated yield.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJC-B Vol.38B(07) [July 1999]en_US
dc.titleSome reactions of 2-phenyl-4(3H)-quinazolinonesen_US
dc.typeArticleen_US
Appears in Collections:IJC-B Vol.38B(07) [July 1999]

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