Microwave-Assisted Regiospecific Synthesis of 2-Trifluoromethyl-7- Trihalomethylated Pyrazolo[1,5-a]Pyrimidines

Author(s): Fernanda A. Rosa, Helio G. Bonacorso, Nilo Zanatta, Alex F.C. Flores, Gabriela F. Fiss, Daniel J. Emmerich, Elisandra Scapin, Marcos A.P. Martins, Wilson Cunico.

Journal Name: Letters in Organic Chemistry

Volume 3 , Issue 5 , 2006

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The reaction of 5-trifluoromethyl-3-aminopyrazole with 1,1,1-trihalo-4-alkoxy-3-alken-2-ones CX3C (O)C(R2) = C(R1)OR, [where R2 = H, Me; R1 = H, alkyl, aryl, OEt and R = alkyl] both in the presence of environmentally benign microwave induced techniques and by the conventional method furnished eleven regiospecific halomethylated pyrazolo[1,5-a]pyrimidines. 1H- and 13C-NMR spectroscopy established that the 7-hydroxy-5-ethoxy-pyrazolo[1,5-a]-6,7-dihydropyrimidine intermediate was also formed.

Keywords: green chemistry, microwave irradiation, enones, pyrazoles, Pyrimidines

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Article Details

Year: 2006
Page: [358 - 362]
Pages: 5
DOI: 10.2174/157017806776611962
Price: $65

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