Abstract:
Hydroxypyrazolidine 1 reacts with 5-aminopyrazoles 2 to form selectively the products of substitution to 4 or 5-aminogroup positions; the isolated intermediate of interaction of noncyclic tautomer 1 with two molecules of aminopyrazole carried out the cyclization into 4-pyrazolidinyl-5-aminopyrazole eliminating one molecule of aminopyrazole
Document Type:
Article
Language: English
Citation:
I. V. Dlinnykh, G. A. Golubeva, P. B. Terentiev, L. A. Sviridova, “Noncyclic intermediate in the synthesis of pyrazolidinylpyrazoles”, Mendeleev Commun., 13:5 (2003), 226–228
Linking options:
https://www.mathnet.ru/eng/mendc4034
https://www.mathnet.ru/eng/mendc/v13/i5/p226
This publication is cited in the following 3 articles:
L. Yet, Comprehensive Heterocyclic Chemistry III, 2008, 1
L. A. Sviridova, G. A. Golubeva, A. N. Tavtorkin, “Synthesis of benzoylmethylpyrazolidine regioisomers on the surface of basic adsorbents: a competitive attack of crotonaldehyde at the two nitrogen atoms of 1,2-acetylphenylhydrazine”, Mendeleev Commun., 15:2 (2005), 66–67
Ilya V. Dlinnykh, Galina A. Golubeva, Petr B. Terentiev, Lyudmila A. Sviridova, “Noncyclic Intermediate in the Synthesis of Pyrazolidinylpyrazoles.”, ChemInform, 35:8 (2004)
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