Synthesis of 5-aminopyrazole-4-carbonitriles

Michael J. Dooley, Ronald J. Quinn, Peter J. Scammells

Research output: Contribution to journalArticleResearchpeer-review

8 Citations (Scopus)

Abstract

A one-pot reaction between substituted hydrazines, malononitrile and triethyl orthoformate leads directly to the formation of 1-substituted 5-aminopyrazole-4-carbonitriles. The scope and limitations of this synthetic procedure are discussed in relation to the well established synthesis of these compounds via substituted hydrazines and ethoxymethylenemalononitrile. © 1989 ASEG.
Original languageEnglish
Pages (from-to)747-750
Number of pages4
JournalAustralian Journal of Chemistry
Volume42
Issue number5
DOIs
Publication statusPublished - 1 Jan 1989

Cite this

Dooley, Michael J. ; Quinn, Ronald J. ; Scammells, Peter J. / Synthesis of 5-aminopyrazole-4-carbonitriles. In: Australian Journal of Chemistry. 1989 ; Vol. 42, No. 5. pp. 747-750.
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Synthesis of 5-aminopyrazole-4-carbonitriles. / Dooley, Michael J.; Quinn, Ronald J.; Scammells, Peter J.

In: Australian Journal of Chemistry, Vol. 42, No. 5, 01.01.1989, p. 747-750.

Research output: Contribution to journalArticleResearchpeer-review

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