Pyrimidines - XLIII. 3,5-diaminopyrazole in the synthesis of pyrazolo[3,4-d]pyrimidines Full article
Journal |
Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353 |
||
---|---|---|---|
Output data | Year: 1976, Volume: 10, Number: 10, Pages: 1248-1250 Pages count : 3 DOI: 10.1007/BF00470175 | ||
Authors |
|
||
Affiliations |
|
Abstract:
In the condensation of benzalbisurea with 1-methyl-3,5-diaminopyrazole the pyrimidine ring closes through the amino group of pyrazole in the 5 position to give 1-methyl-4-phenyl-3-benzalamino-6-oxo-4,5,6,7-tetrahydropyrazolo[3,4-d]pyrimidine. The latter is converted to 1-methyl-4-phenyl-3-amino-6-oxo-6,7-dihydropyrazolo [3,4-d]pyrimidine by dehydrogenation and subsequent hydrolysis of the benzylidene group. © 1976 Plenum Publishing Corporation.
Cite:
Mikhaleva M.A.
, Il'chenko L.N.
, Mamaev V.P.
Pyrimidines - XLIII. 3,5-diaminopyrazole in the synthesis of pyrazolo[3,4-d]pyrimidines
Chemistry of Heterocyclic Compounds. 1976. V.10. N10. P.1248-1250. DOI: 10.1007/BF00470175 Scopus РИНЦ OpenAlex
Pyrimidines - XLIII. 3,5-diaminopyrazole in the synthesis of pyrazolo[3,4-d]pyrimidines
Chemistry of Heterocyclic Compounds. 1976. V.10. N10. P.1248-1250. DOI: 10.1007/BF00470175 Scopus РИНЦ OpenAlex
Dates:
Published print: | Oct 1, 1974 |
Identifiers:
Scopus: | 2-s2.0-34250392067 |
Elibrary: | 30844378 |
OpenAlex: | W2315556914 |