Microwave assisted reactions of some azaheterocylic compounds

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Abstract

A fast, general, environmentally friendly and facile method for preparation of five- and six-membered ring diazaheterocylic salts under microwave irradiation is presented. The N-alkylation reactions of imidazole, pyrimidine, pyridazine and phthalazine have been studied. The microwaves remarkably accelerated these N-alkylations, the reaction times decreased dramatically, the reaction conditions were milder, the consumed energy decreased considerably and the amount of solvents used was reduced substantially. Consequently, the microwave assisted alkylation of N-containing heterocycles could be considered eco-friendly. In some cases, under MW irradiation the yields are also higher. A comparative study of microwave vs. classical conditions (liquid solvents) has been done. Twelve new diazaheterocylic salts of potential practical interest were obtained. © 2009 by the authors; licensee Molecular Diversity Preservation International.

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Zbancioc, G., Bejan, V., Risca, M., Moldoveanu, C., & Mangalagiu, I. I. (2009). Microwave assisted reactions of some azaheterocylic compounds. Molecules, 14(1), 403–411. https://doi.org/10.3390/molecules14010403

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