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
Hauptverfasser: Wang, Jian, Ren, Jiangmeng, Zhu, Yun-Peng, Sun, Xue-Qin, Hu, Peng-Fei, Mu, Xin, Zeng, Bu-Bing
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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.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2022.154312