Completely dissimilar: The reactivity of 1-unsubstituted 3-chloroquinoline-2,4-diones with ethylene diamine and ethanolamine to form new molecular rearrangements

Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F62690094%3A18470%2F20%3A50017571" target="_blank" >RIV/62690094:18470/20:50017571 - isvavai.cz</a>
Alternative codes found
RIV/70883521:28110/20:63526192
Result on the web
<a href="https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p011.053" target="_blank" >https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p011.053</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.24820/ark.5550190.p011.053" target="_blank" >10.24820/ark.5550190.p011.053</a>

Result language
angličtina
Original language name
Completely dissimilar: The reactivity of 1-unsubstituted 3-chloroquinoline-2,4-diones with ethylene diamine and ethanolamine to form new molecular rearrangements
Original language description
3-Chloroquinoline-2,4-diones react with ethanolamine to give 3-hydroxyethylaminoquinoline-2,4-diones. By reacting with isothiocyanic acid, these compounds cyclize to form thioxoimidazo derivatives. If a benzyl group is attached to carbon atom C-3, it is cleaved off. Simultaneously, molecular rearrangement proceeds through the formation of compounds with quinazoline skeletons. However, when using ethylene diamine, the compounds are subject to new types of molecular rearrangement leading to the formation of new quinazoline derivatives.
Czech name
—
Czech description
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Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
—
OECD FORD branch
10401 - Organic chemistry

Project
—
Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Publication year
2020
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

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