Abstract
5-Chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde (1) was reacted with hydrazine hydrate and thiosemicarbazide to afford the corresponding hydrazones 2 and thiosemicarbazones 4. The latter compounds were used to obtain the pyrazole derivatives 3, 5-7. A series of azines 8a-e were obtained by reacting 2 with aromatic aldehydes. Potassium permanganate oxidation of 1 gave the acid 9, which was transformed into the corresponding acid azide 11 then used to prepare diverse urea derivatives 13-18 via Curtius reaction. © ARKAT-USA, Inc.
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Farghaly, A. R., Esmail, S., Abdel-Hafez, A., Vanelle, P., & El-Kashef, H. (2012). New pyrazole derivatives of potential biological activity. Arkivoc, 2012(7), 228–241. https://doi.org/10.3998/ark.5550190.0013.715
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