Spiro-Fused (C2)-Azirino-(C4)-pyrazolones, a New Heterocyclic System. Synthesis, Spectroscopic Studies and X-ray Structure Analysis<sup>1</sup>

Wolfgang Hölzer, Rosa M. Claramunt, Marta Pérez‐Torralba, D. Guggi, T.H. Brehmer

The Journal of Organic Chemistry · 2003 · 29 citations · 16 references

Concepts

Abstract

Reaction of 1-substituted 4-acyl-5-hydroxy-3-methyl-1H-pyrazoles (2) with hydroxylamine gives the corresponding "oximes" 3, which are mainly present as (Z)-2,4-dihydro-4-[(hydroxyamino)methylene]-3H-pyrazol-3-ones. Treatment of compounds 3 with trichloroacetyl isocyanate/potassium carbonate in anhydrous diethyl ether affords 7-methyl-1,5,6-triazaspiro[2.4]hepta-1,6-dien-4-ones (4). The structure of compounds 4 was elucidated by means of single-crystal X-ray analysis (4f, 4h) and confirmed by NMR spectroscopic investigations ((1)H, (13)C).

References

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