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<ArticleSet>
<Article>
<Journal>
				<PublisherName>University of Tehran</PublisherName>
				<JournalTitle>Journal of Sciences, Islamic Republic of Iran</JournalTitle>
				<Issn>1016-1104</Issn>
				<Volume>6</Volume>
				<Issue>1</Issue>
				<PubDate PubStatus="epublish">
					<Year>1995</Year>
					<Month>03</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>NITROIMIDAZOLES XI [I]. SYNTHESES OF
DISUBSTITUTED
NITROIMIDAZOLYLQUINOLINES</ArticleTitle>
<VernacularTitle>-</VernacularTitle>
			<FirstPage></FirstPage>
			<LastPage></LastPage>
			<ELocationID EIdType="pii">31214</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
		    <Abstract>Reaction of substituted-aniline (8) with ethyl (l-methyl-5-nitroimidazole-2-
carbonyl) acetate (9) gave 4-hydroxy-2-(l-methyl-5-nitro-2-imidazolyl)-
substituted-quinolines (lo), which were converted to compound 11 with
phosphorus oxychloride. Substituted-2-(l-methyl-5-nitro-2-imidazo1yl)-4.-
methyl-(or phenyl-) quinolines (14) were prepared through the reaction of 2-
acetyl-5-nitro-1-methyl-imidazole (13) with 0-aminoacetophenones (or Oaminobenzophenones)
in acid medium</Abstract>
<ArchiveCopySource DocType="pdf">https://jsciences.ut.ac.ir/article_31214_d28b6717d8f0015f84b874f9d6688ef7.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
