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Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods
Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods
Scapin, Elisandra; Buriol, Lilian; München, Taiana Scalco; Frizzo, Clarissa Piccinin; Marzari, Mara; Martins, Marcos A. P.
Abstract:
The chemistry of 1,2,4-triazolo[1,5-a]pyrimidine derivatives has been of considerable interest of medicinal and agricultural chemistry for many years. Two very important herbicides, Flumetsulam and Metosulam show acetohydroxyacid synthase inhibitor properties. Other [1,2,4]-triazolo[1,5- a]pyrimidines with antiparasitic, antimicrobial and anticancer activities also are documented. The more related route to 1,2,4-triazolo[1,5-a]pyrimidine is by use of unsymmetrical vinylogous iminium salts. Other route know-well are cyclocondensation reactions of aminoazoles with, _,_-unsaturated ketoesters and aldehydes in multicomponent reactions. In this context, the objective of this work is synthetized 7-aryl(alkyl)1,2,4-triazolo[1,5- a]pyrimidine from ciclocondensation reaction of _- dimethylaminovinyl ketones and 3-amino-1,2,4- triazole.
The chemistry of 1,2,4-triazolo[1,5-a]pyrimidine derivatives has been of considerable interest of medicinal and agricultural chemistry for many years. Two very important herbicides, Flumetsulam and Metosulam show acetohydroxyacid synthase inhibitor properties. Other [1,2,4]-triazolo[1,5- a]pyrimidines with antiparasitic, antimicrobial and anticancer activities also are documented. The more related route to 1,2,4-triazolo[1,5-a]pyrimidine is by use of unsymmetrical vinylogous iminium salts. Other route know-well are cyclocondensation reactions of aminoazoles with, _,_-unsaturated ketoesters and aldehydes in multicomponent reactions. In this context, the objective of this work is synthetized 7-aryl(alkyl)1,2,4-triazolo[1,5- a]pyrimidine from ciclocondensation reaction of _- dimethylaminovinyl ketones and 3-amino-1,2,4- triazole.
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DOI: 10.5151/chempro-14bmos-R0028-1
Referências bibliográficas
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Como citar:
Scapin, Elisandra; Buriol, Lilian; München, Taiana Scalco; Frizzo, Clarissa Piccinin; Marzari, Mara; Martins, Marcos A. P.; "Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods", p-28-28.
In: In Blucher Chemistry Proceedings, São Paulo, v. 1, n. 1, Setembro.2013.
São Paulo: Blucher,
2013.
ISSN 23184043,
DOI 10.5151/chempro-14bmos-R0028-1
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TY - CONF T1 - Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods JO - Blucher Chemistry Proceedings VL - 1 IS - 1 SP - 28 EP - 28 PY - 2013 T2 - Brazilian Meeting on Organic Synthesis 2011 AU - , , , , , SN - 23184043 DO - http://dx.doi.org/10.5151/chempro-14bmos-R0028-1 UR - www.proceedings.blucher.com.br/article-details/synthesis-of-7-arylalkyl124-triazolo15-apyrimidine-using-conventional-methods-7904 KW - ER -
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@article{Scapin20144,
title="Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods",
journal="Blucher Chemistry Proceedings",
volume="1",
number="1",
pages="28 - 28",
year="2013",
note="",
issn="23184043",
doi="http://dx.doi.org/10.5151/chempro-14bmos-R0028-1",
url="www.proceedings.blucher.com.br/article-details/synthesis-of-7-arylalkyl124-triazolo15-apyrimidine-using-conventional-methods-7904",
author="Elisandra Scapin", "Lilian Buriol", "Taiana Scalco München", "Clarissa Piccinin Frizzo", "Mara Marzari", "Marcos A. P. Martins",
keywords="",
}
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Elisandra Scapin, Lilian Buriol, Taiana Scalco München, Clarissa Piccinin Frizzo, Mara Marzari, Marcos A. P. Martins, Synthesis of 7-aryl(alkyl)1,2,4-triazolo[1,5-a]pyrimidine Using Conventional Methods, Blucher Chemistry Proceedings, Volume 1, 2013, Pages 28-28, ISSN 23184043, http://dx.doi.org/10.5151/chempro-14bmos-R0028-1 (www.proceedings.blucher.com.br/article-details/synthesis-of-7-arylalkyl124-triazolo15-apyrimidine-using-conventional-methods-7904) Palavras-chave:: ;