Regiospecific synthesis of 5-trichloromethyl-1H-pyrazole and 1H-pyrazole-5-carboxylic ester derivatives


Autoria(s): MOURA, Sidnei; FLORES, Alex F. C.; PAULA, Favero R.; PINTO, Ernani; MACHADO, Pablo; MARTINS, Marcos A. P.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2008

Resumo

Reaction of 1,1,1-trichloro-4-methoxy-3-penten-2-one (1) with hydrazines (2a-h) (NH2NHR, R = H, Me, t-Bu, Ph, 4-NO2-C6H4, C6F5, CO2Me, CONH2) under differing conditions regiospecifically affords different pyrazole derivatives, 3-methyl-5-trichloromethyl-5-hydroxy-4,5-dihydropyrazoles (3a, d-h), 3-methyl-5-trichloromethyl-1H-pyrazoles (4a,b,d-g) and 5-carboxyethyl-3-methyl-1H-pyrazoles (5a-e). The structural assignments were based on the analysis of their H-1/C-13 NMR and ESI-MS data.

Identificador

LETTERS IN ORGANIC CHEMISTRY, v.5, n.2, p.91-97, 2008

1570-1786

http://producao.usp.br/handle/BDPI/19548

http://apps.isiknowledge.com/InboundService.do?Func=Frame&product=WOS&action=retrieve&SrcApp=EndNote&UT=000254079000005&Init=Yes&SrcAuth=ResearchSoft&mode=FullRecord

Idioma(s)

eng

Publicador

BENTHAM SCIENCE PUBL LTD

Relação

Letters in Organic Chemistry

Direitos

closedAccess

Copyright BENTHAM SCIENCE PUBL LTD

Palavras-Chave #pyrazoles #trichloromethyl-1H-pyrazoles #1,1,1-trichloro-4-alkoxy-3-alken-2-ones #cyclocondensation [CCC plus NN] #REGIOSELECTIVE SYNTHESIS #BIOLOGICAL EVALUATION #PYRAZOLES #AGENTS #INHIBITORS #KETONES #Chemistry, Organic
Tipo

article

original article

publishedVersion