Polyfunctional imidazoles: II. Synthesis and reactions with nucleophilic reagents of 1-substituted 2,4-dichloro-1H-imidazole-5-carbaldehydes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2011-05

AUTHORS

V. A. Chornous, A. M. Grozav, E. B. Rusanov, A. M. Nesterenko, M. V. Vovk

ABSTRACT

1-Alkyl(aryl)imidazolidine-2,4-diones reacted with Vilsmeier-Haack reagent affording 1-alkyl(aryl)-2,4-dichloro-1H-imidazole-5-carbaldehydes whose reactions with sodium azide, sodium alkoholates, with phenols, thiols, and secondary cycloalkylamines led to the substitution of chlorine in the position 2 of the imidazole ring. The reaction with primary amines resulted in the condensation products at the aldehyde group.

PAGES

702

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070428011050083

DOI

http://dx.doi.org/10.1134/s1070428011050083

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1005003075


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