Synthesis of imidazolyl dithiocarbamates and their reactions with phenacyl bromides

The reactions of ethyl (5-carbamoyl-3 H -imidazol-4-yl)dithiocarbamate with phenacyl bromides afford the S-alkylation products as a mixture of E/Z -isomers, which undergo cyclization to 5-(2-oxo-4-arylthiazol-3-yl)-1 H -imidazole-4-carboxamides under the action of a base.

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Veröffentlicht in:Russian chemical bulletin 2011-05, Vol.60 (5), p.882-888
Hauptverfasser: El’tsov, O. S., Mokrushin, V. S., Smirnova, M. V., Shafikov, M. Z.
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Sprache:eng
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Zusammenfassung:The reactions of ethyl (5-carbamoyl-3 H -imidazol-4-yl)dithiocarbamate with phenacyl bromides afford the S-alkylation products as a mixture of E/Z -isomers, which undergo cyclization to 5-(2-oxo-4-arylthiazol-3-yl)-1 H -imidazole-4-carboxamides under the action of a base.
ISSN:1066-5285
1573-9171
DOI:10.1007/s11172-011-0138-3