Reactions of N-(2,2-dichloro-1-cyanoethenyl)-N′-methyl(phenyl)ureas with aliphatic amines View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2017-05

AUTHORS

S. A. Chumachenko, M. V. Kachaeva, O. V. Shablykin, E. B. Rusanov, V. S. Brovarets

ABSTRACT

Novel derivatives of 3,3-dichloroprop-2-enenitrile containing methylurea or phenylurea fragments have been synthesized. The obtained N-(2,2-dichloro-1-cyanoethenyl)-N′-methyl(phenyl)ureas undergo intramolecular cyclization in the presence of triethylamine to form 4-(dichloromethylidene)-5-imino-1-methyl (phenyl)imidazolidin-2-ones. Reactions of N-(2,2-dichloro-1-cyanoethenyl)-N′-methylurea with aliphatic amines have afforded 4-(alkylamino)-4-(dichloromethyl)-5-imino-1-methylimidazolidin-2-ones.

PAGES

985-990

Identifiers

URI

http://scigraph.springernature.com/pub.10.1134/s1070363217050164

DOI

http://dx.doi.org/10.1134/s1070363217050164

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1086045360


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