2004Journal of Chemical ResearchOpen access

Synthesis of Novel Derivatives of 4-Amino-3,5-Dicyanopyrazole

M. Sameiro T. Gonçalves, Ana M. F. Oliveira‐Campos, Lígia M. Rodrigues, M. Fernanda R. P. Proença, John R. Griffiths, Hernâni L. S. Maia, Martin Kaja, Radim Hrdina

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Abstract

Diazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with chloroacetonitrile and triethylamine, as base, gave the corresponding new aminodicyanopyrazoles, in 22–80% yields.

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Diazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with chloroacetonitrile and triethylamine, as base, gave the corresponding new aminodicyanopyrazoles, in 22–80% yields.

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Available abstract

Diazotisation of substituted arylamines followed by reaction with malononitrile gave substituted arylazomalononitriles. Cyclisation of these intermediates with chloroacetonitrile and triethylamine, as base, gave the corresponding new aminodicyanopyrazoles, in 22–80% yields.

Key concepts: Malononitrile, Triethylamine, Base (topology), Chemistry, Organic chemistry, Medicinal chemistry, Combinatorial chemistry, Mathematics

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