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


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Resumo

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.

Sobre autores

S. Chumachenko

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
Ucrânia, ul. Murmanskaya 1, Kiev, 02660

M. Kachaeva

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
Ucrânia, ul. Murmanskaya 1, Kiev, 02660

O. Shablykin

Institute of Bioorganic Chemistry and Petrochemistry

Email: brovarets@bpci.kiev.ua
Ucrânia, ul. Murmanskaya 1, Kiev, 02660

E. Rusanov

Institute of Organic Chemistry

Email: brovarets@bpci.kiev.ua
Ucrânia, Kiev

V. Brovarets

Institute of Bioorganic Chemistry and Petrochemistry

Autor responsável pela correspondência
Email: brovarets@bpci.kiev.ua
Ucrânia, ul. Murmanskaya 1, Kiev, 02660


Declaração de direitos autorais © Pleiades Publishing, Ltd., 2017

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