Improved synthesis of 2-substituted 4-chlorothiazole-5-carbaldehydes
โ Scribed by Norbert Debski; Wolfgang Hanefeld; Martin Schlitzer
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1997
- Tongue
- English
- Weight
- 160 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0022-152X
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โฆ Synopsis
Abstract
An improved method for the reaction of 2,4โdichlorothiazoleโ5โcarbaldehyde (2) with secondary amines was established using potassium carbonate in acetonitrile at room temperature instead of deprotonation with butyllithium in tetrahydrofuran at โ78ยฐ. The method is convenient and the yields of 3 even higher. Compound 2 could also be reacted by this method with thiophenols to yield 4โchloroโ2โphenylthiothiazoleโ5โcarbaldehydes 4.
๐ SIMILAR VOLUMES
Triazoles bearing the appropriate substituents at the 4-and 5-positions can rearran-An interesting application was found re-ge thermally via open-chain diazoirnine intermediates. cently in the transformation of l-phenyl-l,2,3-triazole-4-carbaldehyde into l-alkyl-l,2, 3-triazole-4-carbaldehydes throu
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