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The synthesis of some polycyclic N-H acids with quinoxaline and [1,2,4]triazine cycles

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15410%2F03%3A00001359" target="_blank" >RIV/61989592:15410/03:00001359 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15310/03:00001359

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    The synthesis of some polycyclic N-H acids with quinoxaline and [1,2,4]triazine cycles

  • Original language description

    By diazotization of 3-(4-aminophenyl)-1,2-dihydro-quinoxaline-2-one (2b), 3-(2-aminophenyl)-6,7-dimethyl-1,2-dihydro-quinoxaline-2-one (1b), its 3-(4-aminophenyl)-isomer (3b), 3-(2-aminobenzyl)-1,2-dihydro-quinoxaline-2-one (4b), its 3-(4-aminobenzyl)-isomer (6b), 3-(2-aminobenzyl)-6,7-dimethyl-1,2-dihydro-quinoxaline-2-one (5b) and its 3-(4-aminobenzyl)-isomer (7b) and by azo coupling of formed diazonium salts with ethyl cyanoacetylcarbamate, 3-methyl-1,2-dihydro-quinoxaline-2-one, 3,6,7-trimethyl-1,2-dihydro-quinoxaline-2-one and 3-methyl-6,7-dichloro-1,2-dihydro-quinoxaline-2-one, corresponding hydrazones with one 1,2-dihydro-quinoxaline-2-one ring (1d, 3d, 5d, 7d) and hydrazones with two 1,2-dihydro-quinoxaline-2-one rings (3e-3g, 4e-4g, 5e-5g,6e-6g, 7e-7g) were prepared. Cyclization of hydrazones (1d, 3d, 5d, 7d) afforded compounds (1h, 3h, 5h, 7h) containing 6-azauracile and also 1,2-dihydro-quinoxaline-2-one rings in their molecules. The starting aminoderivative (1b) was prepare

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

    <a href="/en/project/GP204%2F01%2FP117" target="_blank" >GP204/01/P117: Preparation of new anticancer derivatives derived from substituted 1,2,4- and 1,3,5-triazines and study of their molecular and biological effects</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2003

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Arkivoc

  • ISSN

    1424-6376

  • e-ISSN

  • Volume of the periodical

    4

  • Issue of the periodical within the volume

    15

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    10

  • Pages from-to

    65-74

  • UT code for WoS article

  • EID of the result in the Scopus database