The title compounds, obtained by 1,4-addition of sarcosine or glycine ethyl ester on conjugated azoalkenes, gave the 1-ureido-4-amino-3-methyl-1H-pyrazol-5(2H)-ones through a base promoted heterocyclization process, while in the presence of copper (I) species the 1-ureido-5-methyl-4-imidazolines and the 4-methoxycarbonyl-5-methyl-1-ureidoimidazole were obtained. The mechanism of these reactions is discussed.

Base or copper promoted annulation reactions of α-aminohydrazones

ARCADI, Antonio;
1997-01-01

Abstract

The title compounds, obtained by 1,4-addition of sarcosine or glycine ethyl ester on conjugated azoalkenes, gave the 1-ureido-4-amino-3-methyl-1H-pyrazol-5(2H)-ones through a base promoted heterocyclization process, while in the presence of copper (I) species the 1-ureido-5-methyl-4-imidazolines and the 4-methoxycarbonyl-5-methyl-1-ureidoimidazole were obtained. The mechanism of these reactions is discussed.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/17407
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