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 |
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Format: | Artikel |
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. |
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ISSN: | 2046-2069 2046-2069 |
DOI: | 10.1039/c6ra03222b |