Practical povidone iodine catalyzed transamidation from primary amides and amines
[Display omitted] •The transamidation approaching N-substituted amides from various primary amides and amines was achieved with high yields.•The transamidation was catalyzed by non-harmful PVP-I instead of molecule I2.•Several drugs were successfully acquired with a better performance than those pre...
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Veröffentlicht in: | Tetrahedron letters 2023-02, Vol.116, p.154312, Article 154312 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | [Display omitted]
•The transamidation approaching N-substituted amides from various primary amides and amines was achieved with high yields.•The transamidation was catalyzed by non-harmful PVP-I instead of molecule I2.•Several drugs were successfully acquired with a better performance than those previous reported references.
Non-harmful Povidone iodine (PVP-I) was applied in the transamidation to gain N-substituted amides from various primary amides and amines. Diverse aromatic, heterocyclic and aliphatic primary amides/amines were applied in our developed method and more than 45 N-substituted amides were obtained with excellent yields in most cases. Several drugs such as Melatonin and Efaproxiral were successfully acquired with a better performance than those previous reported results. |
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ISSN: | 0040-4039 1873-3581 |
DOI: | 10.1016/j.tetlet.2022.154312 |