Convenient one-pot synthesis of 2-carbamoylmethylthio-3-cyano-4,6-diaryl-5-ethoxycarbonyl-1,4-dihydropyridines

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Abstract

2-Carbamoylmethylthio-3-cyano-4,6-diaryl-5-etfioxycarbonyl-1,4- dihydropyridines 1 were obtained by an one-pot condensation of ethyl 4-nitrobenzoylacetate, an aromatic aldehyde and cyanothioacetamide in the presence of piperidine with subsequent alkylation and dehydroxylation. Thorpe's cyclization of 1 yielded thieno[2,3-b]pyridines 3.

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Krauze, A., Sïle, L., & Duburs, G. (2001). Convenient one-pot synthesis of 2-carbamoylmethylthio-3-cyano-4,6-diaryl-5-ethoxycarbonyl-1,4-dihydropyridines. Heterocyclic Communications, 7(4), 375–380. https://doi.org/10.1515/hc.2001.7.4.375

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