<?xml version="1.0" encoding="UTF-8"?>
<?xml-stylesheet type="text/xsl" href="https://www.eurjchem.com/lib/pkp/xml/oai2.xsl" ?>
<OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/"
	xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
	xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/
		http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd">
	<responseDate>2026-05-04T21:02:19Z</responseDate>
	<request identifier="oai:ojs.www.eurjchem.com:article/479" metadataPrefix="oai_dc" verb="GetRecord">https://www.eurjchem.com/index.php/eurjchem/oai</request>
	<GetRecord>
		<record>
			<header>
				<identifier>oai:ojs.www.eurjchem.com:article/479</identifier>
				<datestamp>2011-12-31T08:09:40Z</datestamp>
				<setSpec>eurjchem:ART</setSpec>
				<setSpec>driver</setSpec>
			</header>
			<metadata>
<oai_dc:dc
	xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"
	xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/
	http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
	<dc:title xml:lang="en-US">Synthesis and reactions of 3-aminotetrachloroquinazolin-2,4-dione</dc:title>
	<dc:creator>Hassan, Mamdouh Adly</dc:creator>
	<dc:creator>Younes, Ahmed Mohamed Mosalem</dc:creator>
	<dc:creator>Taha, Mohamed Mobark</dc:creator>
	<dc:creator>Abdel-Monsef, Abou-Bakr Haredy</dc:creator>
	<dc:subject xml:lang="en-US">Quinazolinedione</dc:subject>
	<dc:subject xml:lang="en-US">Hydrazine hydrate</dc:subject>
	<dc:subject xml:lang="en-US">Anti-inflammatory</dc:subject>
	<dc:subject xml:lang="en-US">Tetrachloroquinazolindione</dc:subject>
	<dc:subject xml:lang="en-US">N-Phenylsulphonyloxytetrachlorophthalimide</dc:subject>
	<dc:subject xml:lang="en-US">3-(N-acetylamino)tetrachloroquinazolindione</dc:subject>
	<dc:description xml:lang="en-US">N-phenylsulphonyloxytetrachlorophthalimide was obtained by treatment of N-hydroxy tetrachlorophthalimide with benzenesulphonyl chloride. Also, the titled compound 3 was obtained by reaction of compound 2 with hydrazine hydrate via Lossen rearrangement. Compound 3 used as starting material for the synthesis of new pyrimidine and quinazolinedione derivatives containing four chlorine atoms which have pharmacological activity.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2011-12-31</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
	<dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
	<dc:format>application/pdf</dc:format>
	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/479</dc:identifier>
	<dc:identifier>10.5155/eurjchem.2.4.514-518.479</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 2 No. 4 (2011): December 2011; 514-518</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
	<dc:relation>https://www.eurjchem.com/index.php/eurjchem/article/view/479/PDF</dc:relation>
</oai_dc:dc>
			</metadata>
		</record>
	</GetRecord>
</OAI-PMH>
