Abstract
4,5-Dihydrodiazoles containing furyl substituents in positions 4 or 6 were obtained by condensation of hydrazine hydrate and 6-ethoxycarbonylcyclohexenones. XSA showed that in the crystalline state, the pyrazolone fragment of the dihydroindazole molecules has a betaine structure.
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Kuban State Technological University, Krasnodar 350072. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1459–1465, November, 1997.
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Usova, E.B., Lysenko, L.I., Krapivin, G.D. et al. Furylcyclohexenones. Conversion of 6-ethoxycarbonylcyclohexenones into 4,5-dihydroindazoles. Molecular and crystal structure of 4-phenyl-6-(5-methyl-2-furyl)-4,5-dihydroindazol-3-one. Chem Heterocycl Compd 33, 1259–1265 (1997). https://doi.org/10.1007/BF02320324
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DOI: https://doi.org/10.1007/BF02320324