Abstract
2-(Chloroselanyl)pyridine reacted with N-vinylpyrrolidin-2-one in chloroform at room temperature to give 3-(2-oxopyrrolidin-1-yl)-2H,3H-[1,3]selenazolo[3,2-a]pyridin-4-ium chloride in quantitative yield.
References
Lukevits, E., Chem. Heterocycl. Compd., 1995, vol. 31, p.639.
Kedarnath, G. and Jain, V.K., Coord. Chem. Rev., 2013, vol. 257, p. 1409.
Zhang, Y., Liu, B., Wu, X., Li, R., Ning, X., Liu, Y., Liu, Z., Ge, Z., Li, R., and Yin, Y., Bioorg. Med. Chem., 2015, vol. 23, p. 4815.
Yoon, D.S., Wu, S.C., Seethala, R., Golla, R., Nayeem, A., Everlof, J.G., Gordon, D.A., Hamann, L.G., and Robl, J.A., Bioorg. Med. Chem. Lett., 2014, vol. 24, p. 5045.
Pan, B.C., Chen, Z.H., Piras, G., Dutschman, G.E., Rowe, E.C., Cheng, Y.C., and Chu, S.H., J. Heterocycl. Chem., 1994, vol. 31, p.177.
Musalov, M.V., Potapov, V.A., and Amosova, S.V., Russ. Chem. Bull., Int. Ed., 2011, vol. 60, p.767.
Potapov, V.A., Malinovich, D.A., Amosova, S.V., Rusakov, Yu.Yu., and Bhasin, K.K., Chem. Heterocycl. Compd., 2012, vol. 48, p. 1129.
Musalov, M.V., Potapov, V.A., Musalova, M.V., and Amosova, S.V., Russ. J. Org. Chem., 2014, vol. 50, p. 1702.
Potapov, V.A., Ishigeev, R.S., and Amosova, S.V., Russ. J. Org. Chem., 2016, vol. 52, p.918.
Borisov, A.V., Matsulevich, Zh.V., Osmanov, V.K., Borisova, G.N., Mamedova, G.Z., Magerramov, A.M., and Khrustalev, V.N., Chem. Heterocycl. Compd., 2012, vol. 48, p. 1098.
Author information
Authors and Affiliations
Corresponding author
Additional information
Original Russian Text © V.A. Potapov, R.S. Ishigeev, S.V. Amosova, 2017, published in Zhurnal Organicheskoi Khimii, 2017, Vol. 53, No. 10, pp. 1568–1569.
Rights and permissions
About this article
Cite this article
Potapov, V.A., Ishigeev, R.S. & Amosova, S.V. Synthesis of 3-(2-oxopyrrolidin-1-yl)-2H,3H-[1,3]selenazolo- [3,2-a]pyridin-4-ium chloride. Russ J Org Chem 53, 1604–1605 (2017). https://doi.org/10.1134/S1070428017100219
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070428017100219