Microwave Assisted Synthesis and Unusual Coupling of Some Novel Pyrido[3,2-F][1,4]Thiazepines

Citation:
Faty, R. A. A. M., "Microwave Assisted Synthesis and Unusual Coupling of Some Novel Pyrido[3,2-F][1,4]Thiazepines", Molecules, 2011.

Abstract:

3-Amino-3-thioxopropanamide (1) reacted with ethyl acetoacetate to form6-hydroxy-4-methyl-2-thioxo-2,3-dihydropyridine-3-carboxamide (2), which reacted with ?-haloketones 3 to produce 2,3-disubstituted-8-hydroxy-6-methyl-2H,5H-pyrido[3,2-f]-[1,4] thiazepin-5-ones 4a-c. Benzoylation of 4c led to the formation of the dibenzoate derivative 9. Compounds 4a-c could be prepared stepwise through the formation of S-alkylated derivatives 10a-c. Compounds 2, 4a-c, 9 and 10a-c were prepared using microwave as a source of heat, and gave better yields in shorter times than those achieved by traditional methods. Coupling of 4a-c with arenediazonium chlorides proceeded unusually to give the 6-hydroxy-4-methyl-2-(arylazo)thieno[2,3-b]pyridin-3(2H)-one ring contraction products 14. Structures of the newly synthesized compounds were proven by spectral and chemical methods.

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