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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.7//EN" "https://dtd.nlm.nih.gov/ncbi/pubmed/in/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
				<PublisherName></PublisherName>
				<JournalTitle>Iranian chemical communication</JournalTitle>
				<Issn>2423-4958</Issn>
				<Volume>3</Volume>
				<Issue>Issue 2, pp. 72-147, Serial No. 7</Issue>
				<PubDate PubStatus="epublish">
					<Year>2015</Year>
					<Month>04</Month>
					<Day>01</Day>
				</PubDate>
			</Journal>
<ArticleTitle>A new facile route to synthesize thieno[3,2-e][1,2,4]triazolo[4,3-c]pyrimidine derivatives</ArticleTitle>
<VernacularTitle></VernacularTitle>
			<FirstPage>114</FirstPage>
			<LastPage>120</LastPage>
			<ELocationID EIdType="pii">990</ELocationID>
			
			
			<Language>EN</Language>
<AuthorList>
<Author>
					<FirstName>Mehdi</FirstName>
					<LastName>Soleimany</LastName>
<Affiliation>Payame Noor University (PNU)</Affiliation>

</Author>
<Author>
					<FirstName>Jalil</FirstName>
					<LastName>Lari</LastName>
<Affiliation>Payame Noor University of Mashhad</Affiliation>

</Author>
<Author>
					<FirstName>Hooshang</FirstName>
					<LastName>Vahedi</LastName>
<Affiliation>Payame Noor University of Mashhad</Affiliation>

</Author>
<Author>
					<FirstName>Morteza</FirstName>
					<LastName>Imanpour</LastName>
<Affiliation>Payame Noor University of Mashhad</Affiliation>

</Author>
</AuthorList>
				<PublicationType>Journal Article</PublicationType>
			<History>
				<PubDate PubStatus="received">
					<Year>2014</Year>
					<Month>07</Month>
					<Day>02</Day>
				</PubDate>
			</History>
		<Abstract>A new facile route for synthesis of 3- (aryl) -8, 9- di (alkyl) thieno [3,2-e] [1,2,4] triazolo pyrimidines derivative from the same starting material, 2- amino - 4,5 -di (alkyl) thiophene-3- carboxamide, has been developed through heterocyclization of the corresponding arylidene-hydrazino -5,6 -di (alkyl) thieno [2,3-d] pyrimidine under refluxing condition with acetic anhydride followed by air oxidation. The products were obtained in high yield with an easy work-up in simple reaction along with the puriﬁcation of products by non-chromatographic method. This general synthetic procedure can be extended to the preparation of a wide variety of isomeric triazoles using 2-amino thiophene-3-carboxamide bifunctional derivatives.</Abstract>
		<ObjectList>
			<Object Type="keyword">
			<Param Name="value">Thieno[3</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">2-e][1</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">2</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">4]triazolo[4</Param>
			</Object>
			<Object Type="keyword">
			<Param Name="value">3-c]pyrimidines heterocyclization acetic anhydride air oxidation</Param>
			</Object>
		</ObjectList>
<ArchiveCopySource DocType="pdf">https://icc.journals.pnu.ac.ir/article_990_64c0478c874aeb47e50c95b79b0dacdb.pdf</ArchiveCopySource>
</Article>
</ArticleSet>
