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Synthesis 2022; 54(16): 3658-3666
DOI: 10.1055/s-0041-1738070
DOI: 10.1055/s-0041-1738070
paper
One-Pot Syntheses of Substituted 2-Aminothiazoles and 2-Aminoselenazoles via Meerwein Arylation of Alkyl Vinyl Ketones
The authors thank the National Research Foundation of Ukraine (Project 2020.01/0166 ‘New azole and cage-like agents against cancer and pathogenic microorganisms’).
Abstract
Both one-pot and two-step procedures for the synthesis of substituted 2-aminothiazoles and 2-aminoselenazoles are described. Anilines are first converted into arenediazonium bromides, which are then reacted with methyl vinyl ketone or cyclopropyl vinyl ketone in the presence of copper(II) bromide to give 4-aryl-3-bromobutan-2-ones (40–71%) and 3-aryl-2-bromo-1-cyclopropylpropan-1-ones (41–79%), respectively. These products are reacted, without prior isolation, with thiourea or selenourea to prepare 4-methyl- and 4-cyclopropyl-5-(R-benzyl)thiazol-2-amines (14 examples) and their selenium analogs (14 examples). The yields of the one-pot procedure are higher (40–81%) than those of the two-step procedure (32–70%).
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0041-1738070.
- Supporting Information
Publikationsverlauf
Eingereicht: 02. März 2022
Angenommen nach Revision: 28. März 2022
Artikel online veröffentlicht:
03. Mai 2022
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