SYNTHESIS OF 1,2,4-TRIAZOL-5-YLAMINO PYRIMIDINES TRIFLUOROMETHYL SUBSTITUTED / SÍNTESE DE 1,2,4-TRIAZOL-5-ILAMINO PIRIMIDINAS TRIFLUORMETIL SUBSTITUÍDAS
AUTOR(ES)
Guilherme Pivotto Bortolotto
DATA DE PUBLICAÇÃO
2009
RESUMO
This work describes the synthesis and characterization of fourteen 4-trifluoromethyl-2-[3-(pyridyl)-1H-1,2,4-triazol-5-ylamino]pyrimidines (6, 7), from the cyclocondensation reaction of N-[3-(pyridyl)-1H-1,2,4-triazol-5-yl]guanidines (4, 5), a 1,3-dinucleophile precursor of the type (N-C-N), with 1,1,1-trifluoro-4-alkoxy-3-alken-2-ones (1), a versatile 1,3-dieletrophile. The 1,1,1-trifluoro-4-alkoxy-3-alken-2-ones (1), of the general formula F3C-C(O)- CH=C(R)-OR1 where R1 = Me, Et and R = H, Me, Ph, 4-FPh, 4-MePh, 4-OMePh, Furyl, were obtained from trifluoroacetylation reactions of enolethers or acetals derived of acyclic ketones. The reactions of 1,1,1-trifluoro-4-alkoxy-3-alken-2-ones (1) with N-[3-(pyridyl)-1H-1,2,4-triazol-5-yl]guanidines (4, 5) was carried in ethanol in reflux for 18 hours, leading to end products in 40-68% yield. The compounds were characterized by 1H and 13C NMR experiments, and the purity these compounds proved by elemental analysis.
ASSUNTO(S)
pirimidinas acetais quimica química espectrometria
ACESSO AO ARTIGO
http://coralx.ufsm.br/tede/tde_busca/arquivo.php?codArquivo=2868Documentos Relacionados
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