1-Aryl-6-azauracils XL. Synthesis of some 1-(1-phenyl-3-pyrazolyl)-derivatives.

Result code in IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F00%3A00000942" target="_blank" >RIV/61989592:15310/00:00000942 - isvavai.cz</a>

Result on the web

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DOI - Digital Object Identifier

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Result language

angličtina

Original language name

1-Aryl-6-azauracils XL. Synthesis of some 1-(1-phenyl-3-pyrazolyl)-derivatives.

Original language description

The appropriate hydrazone was obtained by the diazotation of 1-phenyl-3-aminopyrazole and by the following coupling reaction of formed diazonium salt with ethyl cyanoacetyl carbamate. The cyclization of this hydrazone does not undergo to the appropriatederivative pyrazolo[5,1-c][1,2,4]triazine, but both the thermal and the alkaline cyclization undergoes to 1-(1-phenyl-3-pyrazolyl)-6-azauracil-5-carbonitrile.

Czech name

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Czech description

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Type

J_x - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

CEP classification

CC - Organic chemistry

OECD FORD branch

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Project

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Continuities

Z - Vyzkumny zamer (s odkazem do CEZ)

Publication year

2000

Confidentiality

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Name of the periodical

Acta Universitatis Palackianae Olomucensis, Facultas Rerum Naturalium, Chemica

ISSN

0232-0061

e-ISSN

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Volume of the periodical

39

Issue of the periodical within the volume

NA

Country of publishing house

XX - stateless person

Number of pages

8

Pages from-to

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UT code for WoS article

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EID of the result in the Scopus database

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