One‐pot synthesis of highly functionalized benzo [1,3] thiazine from isocyanides,aniline, and heterocumulene via Cu‐catalyzed intramolecular C‐H activation reactions |
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Authors: | Hossein F. Dastjerdi Manijeh Nematpour Elham Rezaee Mehdi Jahani Sayyed A. Tabatabai |
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Abstract: | A one‐pot synthesis of functionalized benzo thiazine derivatives via a Cu‐catalyzed, multicomponent reaction of isocyanides, aniline, and heterocumulenes in acetonitrile at room temperature was developed. Transition metal‐catalyzed activation of C‐H bonds under mild copper‐catalytic reaction conditions, using simple and available starting materials, also obtaining a pure product with high yield without applying column chromatography are the major advantages of the applied method among the other ones used for this purpose. The structures are confirmed spectroscopically (1H‐ and 13C‐NMR, IR, and EI‐MS) and through elemental analyses. |
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Keywords: | aniline benzo [1, 3] thiazine C‐H activation copper iodide heterocumulene isocyanides |
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