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


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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.

About the authors

S. A. Chumachenko

Institute of Bioorganic Chemistry and Petrochemistry

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

M. V. Kachaeva

Institute of Bioorganic Chemistry and Petrochemistry

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

O. V. Shablykin

Institute of Bioorganic Chemistry and Petrochemistry

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

E. B. Rusanov

Institute of Organic Chemistry

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

V. S. Brovarets

Institute of Bioorganic Chemistry and Petrochemistry

Author for correspondence.
Email: brovarets@bpci.kiev.ua
Ukraine, ul. Murmanskaya 1, Kiev, 02660


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