Poly(ethylene) glycols and mechanochemistry for the preparation of bioactive 3,5-disubstituted hydantoins

Mechanochemistry was effective for the preparation of 3,5-disubstituted hydantoins from -amino methyl esters, using either 1,1-carbonyldiimidazole (CDI) or alkyl isocyanates. The preparation of the antimicrobial additives, 3-allyl-5,5-dimethyl hydantoin (ADMH) and 1-chloro-3-ethyl-5,5-dimethyl hydan...

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Veröffentlicht in:RSC advances 2016-01, Vol.6 (43), p.36978-36986
Hauptverfasser: Konnert, L, Dimassi, M, Gonnet, L, Lamaty, F, Martinez, J, Colacino, E
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Sprache:eng
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Zusammenfassung:Mechanochemistry was effective for the preparation of 3,5-disubstituted hydantoins from -amino methyl esters, using either 1,1-carbonyldiimidazole (CDI) or alkyl isocyanates. The preparation of the antimicrobial additives, 3-allyl-5,5-dimethyl hydantoin (ADMH) and 1-chloro-3-ethyl-5,5-dimethyl hydantoin (CEDMH) were performed by grinding. A chlorination reaction, never described before by mechanochemistry was achieved by Ca(ClO) 2 , while the preparation of the bioactive anticonvulsant marketed drug ethotoin was achieved by a novel approach based on poly(ethylene) glycol (PEGs) assisted grinding. Mechanochemistry was effective for the preparation of 3,5-disubstituted hydantoins from -amino methyl esters, using either 1,1-carbonyldiimidazole (CDI) or alkyl isocyanates.
ISSN:2046-2069
2046-2069
DOI:10.1039/c6ra03222b