Abstract
Alkaline hydrolysis of 1-(2,3-dihydro-1,4-benzodioxin-6-yl)cyclopentane-1-carbonitrile gave the corresponding carboxylic acid which was converted to carbonyl chloride, and the latter reacted with N, N-di-alkylalkane-α,ω-diamines and dialkylaminoalkanols to afford new amino amides and amino esters which were isolated as hydrochlorides. Anticonvulsant activity of the synthesized compounds was studied.
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Arustamyan, Zh.S., Markaryan, R.E., Agekyan, A.A., Stepanyan, G.M., Paronikyan, R.V, Shirinyan, E.A., Noravyan O.S., and Minasyan, N.S., Khim. Zh. Arm., 2014, vol. 67, p. 92.
Airapetyan, G.K., Akopyan, M.G., Arustamyan, Zh.S., and Markaryan, E.A., Chem. Heterocycl. Compd., 1993, vol. 29, p. 578. doi https://doi.org/10.1007/BF00534473
Kankanala, J., Marchand, Ch., Abdelmalak, M., Aihara, H., Pommier, Y., and Wang, S., J. Med. Chem., 2016, vol. 59, p. 2734. doi https://doi.org/10.1021/acs.jmedchem.5b01973
Davies, S.G., Fletcher, A.M., Frost, A.B., Kennedi, M.S., Roberts, P.M., and Thomson, J.E., Tetrahedron, 2016, vol. 72, p. 2139. doi https://doi.org/10.1016/j.tet.2016.03.008
Vogel, H.G. and Vogel, W.H., Drug Discovery and Evaluation: Pharmacological Assays, Vogel, H.G., Ed., Berlin: Springer, 2008, 3rd ed., p. 565.
Belen’kii M.L., Elementy kolichestvennoi otsenki farmakologicheskogo effekta (Elements of Quantitative Evaluation of Pharmacological Effect), Leningrad: Meditsina, 1961.
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Russian Text © The Author(s), 2019, published in Zhurnal Organicheskoi Khimii, 2019, Vol. 55, No. 6, pp. 896–900.
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Arustamyan, Z.S., Markaryan, R.E., Aghekyan, A.A. et al. Synthesis and Anticonvulsant Activity of Amino Amides and Amino Esters Based on 1-(2,3-Dihydro-1,4-benzodioxin-6-yl)-cyclopentane-1-carboxylic Acid. Russ J Org Chem 55, 796–799 (2019). https://doi.org/10.1134/S1070428019060095
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DOI: https://doi.org/10.1134/S1070428019060095