Artículo
Autoría
PLEM, SILVANA CRISTINA
;
Müller, Diana
;
MURGUIA, MARCELO CESAR
Fecha
2015
Editorial y Lugar de Edición
Scientific Research Publishing
Revista
Advances in Chemical Engineering and Science,
vol. 5
(pp. 239-261)
- ISSN 2160-0406
Scientific Research Publishing
Scientific Research Publishing
ISSN
2160-0406
Resumen
Información suministrada por el agente en
SIGEVA
A series of six pyrazoles was synthesized by Michael-type addition reaction. The molecules 5- amino-1-aryl-1H-pyrazole-4-carbonitrile (3a-f) were synthesized from (ethoxymethylene)malononitrile (1) and fluorinated and non-fluorinated aryl hydrazines (2a-f) using ethanol and fluorinated ethanol as solvents at reflux. An excellent regio-selectivity was found when pyrazole derivatives were formed as an exclusive product. No other regioisomer or uncyclised hydrazide was observed. Their structures w...
A series of six pyrazoles was synthesized by Michael-type addition reaction. The molecules 5- amino-1-aryl-1H-pyrazole-4-carbonitrile (3a-f) were synthesized from (ethoxymethylene)malononitrile (1) and fluorinated and non-fluorinated aryl hydrazines (2a-f) using ethanol and fluorinated ethanol as solvents at reflux. An excellent regio-selectivity was found when pyrazole derivatives were formed as an exclusive product. No other regioisomer or uncyclised hydrazide was observed. Their structures were confirmed by spectroscopy data (1H, 13C, 19F, COSY (correlation spectroscopy), HSQC (heteronuclear single-quantum correlation spectroscopy) and HMBC (heteronuclear multiple-bond correlation spectroscopy); MS (mass-spectrometry). The yields ranged from good to excellent (47% - 93%) under mild reaction conditions. It would indicate a high selectivity in the one-step work procedure. These products (3a-f) and derivatives have a potential academic and industrial use as key intermediates, in special, for application in crop protection.
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Palabras Clave
5-AMINO-1-ARYL-1H-PYRAZOLES-4-CARBONITRILESAMINO PYRAZOLEARYL HYDRAZINE
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