Abstract
Microwave reactions of primary and secondary amines with imidoylbenzotriazoles 6a-w gave diversely substituted amidines 7a-Aa in 76-94% yields. Convenient preparations of a variety of amides 5a-Ab (87-96%) and imidoylbenzotriazoles 6a-w (56-95%) have also been developed using microwave irradiation under mild conditions and short reaction times. These results demonstrate further the advantages of microwave synthesis and introduce a new application of imidoylbenzotriazoles in the preparation of polysubstituted amidines. © 2006 American Chemical Society.
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CITATION STYLE
Katritzky, A. R., Cai, C., & Singh, S. K. (2006). Efficient microwave access to polysubstituted amidines from imidoylbenzotriazoles. Journal of Organic Chemistry, 71(9), 3375–3380. https://doi.org/10.1021/jo052443x
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