Regiospecific synthesis of 5-trichloromethyl-1H-pyrazole and 1H-pyrazole-5-carboxylic ester derivatives
| Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
|---|---|
| Data(s) |
19/10/2012
19/10/2012
2008
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| 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 |
| 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 |