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Synthesis of new tetrahydropyrido[1,2-a]benzimidazoles based on recyclization of N-arylitaconimides with 2-cyanomethylbenzimidazole Full article

Journal Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Output data Year: 2021, Volume: 31, Number: 2, Pages: 254-256 Pages count : 3 DOI: 10.1016/j.mencom.2021.03.037
Authors Shmoylova Yana Yu. 1 , Kovygin Yuri A. 1 , Ledenyova Irina V. 1 , Prezent Mikhail A. 2 , Baranin Sergey V. 2 , Shikhaliev Khidmet S. 1
Affiliations
1 Voronezh State University, 394018 Voronezh, Russian Federation
2 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Abstract: A convenient preparative synthesis of N-aryl-2-(4-cyano-3-oxo-1,2,3,5-tetrahydropyrido[1,2-a]benzimidazol-2-yl)acetamides is based on the reflux of N-arylitaconimides with 2-cyanomethylbenzimidazole in acetic acid.
Cite: Shmoylova Y.Y. , Kovygin Y.A. , Ledenyova I.V. , Prezent M.A. , Baranin S.V. , Shikhaliev K.S.
Synthesis of new tetrahydropyrido[1,2-a]benzimidazoles based on recyclization of N-arylitaconimides with 2-cyanomethylbenzimidazole
Mendeleev Communications. 2021. V.31. N2. P.254-256. DOI: 10.1016/j.mencom.2021.03.037 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000635839800037
≡ Scopus: 2-s2.0-85105008497
≡ OpenAlex: W3144659209
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