Synthesis of analogs of 5(4)-aminoimidazole-4(5)-carboxamide and purines - 8. Some reactions of 5(4)-aminoimidazole-4(5)-carboxhydrazide / Nifontov V.I., Selezneva I.S., Mokrushin V.S., Pushkareva Z.V., Trofimov V.A. // Chemistry of Heterocyclic Compounds. - 1979. - V. 15, l. 7. - P. 805-806.

ISSN:
00093122
Type:
Article
Abstract:
5-Diazoimidazole-4-carboxazide was isolated in the diazotization of 5(4)-aminoimidazole-4(5)-carboxhydrazide. The diazotization of N-substituted hydrazides of 5(4)-aminoimidazole-4(5)-carboxylic acis was studied. It is shown that the resulting diazo derivatives undergo cyclization to 3-arylideneaminoimidazo[4,5-d]-1,2,3-triazin-4-ones. © 1980 Plenum Publishing Corporation.
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DOI:
10.1007/BF00473569
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Affiliations S. M. Kirov Ural Polytechnic Institute, Sverdlovsk, 620002, Russian Federation
References Bakulev, V.A., Mokrushin, V.S., Ofitserov, V.I., Pushkareva, Z.V., Grishakov, A.N., (1979) Khim. Geterotsikl. Soedin., 6, p. 836; Peters, D.A., McGeer, P.L., Inhibition of purine biosynthesis by analogues of 4(5)-aminoimidazole-5(4)-carboxamide (1968) Canadian Journal of Physiology and Pharmacology, 46, p. 195; Barton, D.H.R., O'Brien, R.E., Sternhell, S., (1962) J. Chem. Soc., 2, p. 470
Correspondence Address Nifontov, V.I.; S. M. Kirov Ural Polytechnic Institute, Sverdlovsk, 620002, Russian Federation
Publisher Kluwer Academic Publishers-Plenum Publishers
CODEN CHCCA
Language of Original Document English
Abbreviated Source Title Chem Heterocycl Compd
Source Scopus