An approach to the synthesis of 4-unsubstituted 2-(2-oxo-1,2-dihydro-3H-pyrrol-3-ylidene)malononitriles
- Authors: Blinov S.A1, Belikov M.Y.1
-
Affiliations:
- Chuvash State University named after I.N. Ulyanov
- Issue: Vol 61, No 11 (2025)
- Pages: 1580–1584
- Section: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://journals.rcsi.science/0514-7492/article/view/381754
- DOI: https://doi.org/10.7868/S3034630425110062
- ID: 381754
Cite item
Abstract
A method for the synthesis of pyrrol-2-one derivatives containing a yidenemalononitrile fragment in their structure has been developed. Their preparation is based on the initial interaction of furan-2-ones with ammonia, leading to the formation of γ-oxobutanamide intermediates. These compounds subsequently react with tetracyanoethylene, transforming into the target pyrrole derivatives.
Keywords
About the authors
S. A Blinov
Chuvash State University named after I.N. Ulyanov
ORCID iD: 0009-0009-9001-6033
Cheboksary, Russia
M. Yu Belikov
Chuvash State University named after I.N. Ulyanov
Email: belikovmil@mail.ru
ORCID iD: 0000-0001-6444-3810
Cheboksary, Russia
References
- Milovidova A.G., Belikov M.Yu., Ievlev M.Yu., Nasakin O.E., Ershov O.V., Tafeenko V.A. Synth. Commun. 2021, 51, 727–737. https://doi.org/10.1080/00397911.2020.1852434
- Belikov M.Yu., Milovidova A.G., Ievlev M.Yu. New. J. Chem. 2022, 46, 7845–7849. https://doi.org/10.1039/D2NJ01131J
- Belikov M.Yu., Milovidova A.G., Ievlev M.Yu., Fedoseev S.V. Org. Biomol. Chem. 2024, 22, 4757–4765. https://doi.org/10.1039/d4ob00612g
- Belikov M.Yu., Milovidova A.G., Ievlev M.Yu. Chemistry-Select. 2024, 9, e202400788. https://doi.org/10.1002/slct.202400788
- Belikov M.Yu., Ershov O.V., Eremkin A.V., Nasakin O.E., Tafeenko V.A., Nurieva E.V. Tetrahedron Lett. 2011, 52, 6407–6410. https://doi.org/10.1016/j.tetlet.2011.09.084
- Cutillas-Font G., Pastor A., Alajarin M., Martinez-Cuezva A., Marin-Luna M., Batanero B., Berna J. Chem. Sci. 2024, 15, 13823–13831. https://doi.org/10.1039/D4SC03657C
- Luo H., Dong X., Cai Z., Wang L., Liu Z. Asian J. Org. Chem. 2018, 7, 592–597. https://doi.org/10.1002/ajoc.201700669
- Burgess J., Steel P.J. Tetrahedron Lett. 2006, 47, 4107–4108. https://doi.org/10.1016/j.tetlet.2006.04.084
- Dworczak R., Sterk H., Junek H. Monatsh Chem. 1990, 121, 189–193. https://doi.org/10.1007/BF00809531
- Abd El-Nabi H.A. Tetrahedron. 2002, 58, 135–141. https://doi.org/10.1016/S0040-4020(01)01029-8
- El-Gaby M.S.A., El-Hag Ali G.A.M., El-Maghraby A.A., Abd El-Rahman M.T., Helal M.H.M. Eur. J. Med. Chem. 2009, 44, 4148–4152. https://doi.org/10.1016/j.ejmech.2009.05.005
- Aly M.M. Phosphorus Sulfur Silicon Rel. Elem. 2007, 182, 1497–1506. https://doi.org/10.1080/10426500701242954
- Turova O.V., Berezhnaya V.G., Starodubtseva E.V., Ferapontov V.A., Vinogradov M.G. Russ. Chem. Bull. 2015, 64, 859–863. https://doi.org/10.1007/s11172-015-0945-z
- Lill A.P., Rodl C.B., Steinhilber D., Stark H., Hofmann B. Eur. J. Med. Chem. 2015, 89, 503–523. https://doi.org/10.1016/j.ejmech.2014.10.054
Supplementary files


