Abstract
Acylation of 2-amino-5,5-dimethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carbonitrile and 2-amino-4,5,6,7-tetrahydro-1-benzothiophene-3-carbonitrile with various acids chlorides in anhydrous dioxane furnished the corresponding amides. Coordination compounds were obtained by reacting copper(II) chloride, zinc(II), cobalt(II), and barium(II) acetates with N-(5,5-dimethyl-3-cyano-4,7-dihydro-5H-thieno[2,3-c]pyran-2-yl)-4-chlorobutanamide. Anti-MAO activity of the synthesized compounds was studied.
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Isakhanyan, A.U., Hakobyan, N.Z., Grigoryan, A.S. et al. Synthesis and Anti-MAO Activity of Acylation Products of Annelated Thiophene-2-amine and N-(5,5-Dimethyl-3-cyano-4,7-dihydro-5H-thieno[2,3-c]pyran-2-yl)-4-chlorobutanamide and Their Complexes with Cu(II), Zn(II), Ba(II), and Co(II). Russ J Gen Chem 92, 2516–2520 (2022). https://doi.org/10.1134/S1070363222110391
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DOI: https://doi.org/10.1134/S1070363222110391