Issue 0, 1981

Allenes. Part 39. The synthesis of 3-alkyl-5-aminopyrazoles and 3H-indoles from allenic or acetylenic nitriles

Abstract

Hydrazine adds to allenic or acetylenic nitriles to give 3-alkyl-substituted 5-aminopyrazoles in excellent yields. Conjugated and unconjugated enaminic nitriles may be isolated from the Michael addition of phenylhydrazine to allenic nitriles and ring-closed to give 3-alkyl-5-amino-N-phenylpyrazoles and 3H-indoles.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 2997-3001

Allenes. Part 39. The synthesis of 3-alkyl-5-aminopyrazoles and 3H-indoles from allenic or acetylenic nitriles

Z. T. Fomum, S. R. Landor, P. D. Landor and G. W. P. Mpango, J. Chem. Soc., Perkin Trans. 1, 1981, 2997 DOI: 10.1039/P19810002997

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