Synthesis and Structure of Diethyl 2-[(Aryl)-(Morpholino/Piperidin-1-Yl)Methyl]Malonates
- Authors: Podchezertseva K.V.1, Homan A.S.1, Zamaraeva T.M.1, Dmitriev M.V.2
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Affiliations:
- Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
- Perm State National Research University
- Issue: Vol 95, No 7-8 (2025)
- Pages: 240-244
- Section: Articles
- URL: https://vietnamjournal.ru/0044-460X/article/view/692695
- DOI: https://doi.org/10.31857/S0044460X25070019
- EDN: https://elibrary.ru/spkqbk
- ID: 692695
Cite item
Abstract
A three-component reaction of diethyl malonate with aromatic aldehyde, morpholine or piperidine during boiling in ethanol for 4 h produced diethyl 2-[(aryl)(morpholino/piperidin-1-yl)methyl]malonates. Structure of the compounds was determined by 1H, 13C NMR spectroscopy and single crystal X-ray diffraction analysis.
About the authors
K. V. Podchezertseva
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
Email: tanyapgfa@yandex.ru
Perm, 614990 Russia
A. S. Homan
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
Email: tanyapgfa@yandex.ru
Perm, 614990 Russia
T. M. Zamaraeva
Perm State Pharmaceutical Academy of the Ministry of Health of the Russian Federation
Email: tanyapgfa@yandex.ru
Perm, 614990 Russia
M. V. Dmitriev
Perm State National Research University
Author for correspondence.
Email: tanyapgfa@yandex.ru
Perm, 614068 Russia
References
- Maquoi E., Sounni N.E., Devy L., Olivier F., Frankenne F., Krell H.-W., Grams F., Foidart J.-M., Noёl A. // Clin. Canc. Res. 2004. Vol. 10. P. 4047. doi: 10.1158/1078-0432.CCR-04-0125
- Lakomska I., Hoffmann K., Wojtczak A., Sitkowski J., Maj E., Wietrzyk J. // J. Inorg. Biochem. 2014. Vol. 141. P. 188. doi: 10.1016/j.jinorgbio.2014.08.005
- Kadi I., Güldeniz Ş., Boulebd H., Zebbiche Z., Suat T., Fatümetüzzehra K., Boumoud T. // Polycycl. Arom. Compd. 2023. P. 1. doi: 10.1080/10406638.2023.2281468
- Guo T., Xia R., Liu T., Peng F., Tang X., Zhou Q., Luo H., Xue W. // Chem. Biodivers. 2020. Vol. 17. P. e2000025. doi: 10.1002/cbdv.202000025
- Zhang S., Cheng K., Wang X., Yin H. // Bioorg. Med. Chem. 2012. Vol. 20. N 20. P. 6073. doi: 10.1016/j.bmc.2012.08.022
- Karumanchi K., Natarajan S.K., Gadde S., Chavakula R., Korupolu R.B., Bonige K.B. // Synth. Commun. 2019. Vol. 49. N 3. P. 359. doi: 10.1080/00397911.2018.1550200
- Zhou Z., Chen F., Xu G., Gou S. // Bioorg. Med. Chem. Lett. 2016. Vol. 26. N 2. P. 322. doi: 10.1016/j.bmcl.2015.12.019
- Liu Y., Zhou X., Shang D., Liu X., Feng X. // Tetrahedron. 2010. Vol. 66. P. 1447. doi: 10.1016/j.tet.2009.12.032
- Meskini I., Daoudi M., Daran J.-C., Zouihri H., Ben Hadda T. // Acta Crystallogr. (E). 2010. Vol. 66. P. o1014. doi: 10.1107/S1600536810025572
- Mokale S.N. // J. Chem. Pharm. Res. 2013. Vol. 5. N 12. Р. 1009.
- Akkurt M., Yildirim S.O., Benjelloun O.T., Ben Larbi N., Ben Hadda T., Buyukgundor O. // Acta Crystallogr. (E). 2007. Vol. 63. P. o1656. doi: 10.1107/S1600536807010380
- Shreekanth T.K., Yathirajan H.S., Kalluraya B., Foro S., Glidewell C. // Acta Crystallogr. (E). 2020. Vol. 76. P. 1605. doi: 10.1107/S2056989020011676
- Подчезерцева К.В., Замараева Т.М., Дмитриев М.В. // ЖОХ. 2024. Т. 94. № 3. С. 364. doi: 10.31857/S0044460X24030069
- O’Callaghan C.N. // J. Chem. Soc. Perkin Trans. I. 1972. P. 1416.
- Хамитова А.Е., Берилло Д.А. // Разработка и регистрация лекарственных средств. 2023. Т. 12. № 2. С. 44. doi: 10.33380/2305-2066-2023-12-2-44-54
- Kourounakis A.P., Xanthopoulos D., Tzara A. // Med. Res. Rev. 2020. Vol. 40. N 2. P. 709. doi: 10.1002/med.21634
- CrysAlisPro, Rigaku Oxford Diffraction, 2022, Version 1.171.42.74a.
- Sheldrick G.M. // Acta Crystallogr. (A). 2015. Vol. 71. P. 3. doi: 10.1107/S2053273314026370
- Sheldrick G.M. // Acta Crystallogr. (C). 2015. Vol. 71. P. 3. doi: 10.1107/S2053229614024218
- Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. // J. Appl. Cryst. 2009. Vol. 42. P. 339. doi: 10.1107/S0021889808042726
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