Abstract
4,5-Dibenzoyl-1H-pyrrole-2,3-diones and 4-benzoyl-5-phenyl-1H-pyrrole-2,3-diones reacted with 3-arylamino-1H-inden-1-ones at a molar ratio of 1:2 to give substituted spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. The molecular and crystal structures of 4′,5′-dibenzoyl-1′-(4-methoxyphenyl)-5-phenyl-5H-spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrrole]-2′,10,12(1′H)-trione were determined by X-ray analysis.
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Funding
This study was performed under financial support by the Ministry of Science and Higher Education of the Russian Federation (project nos. 4.6774.2017/8.9, 4.5894.2017/7.8), by the Russian Foundation for Basic Research (project no. 16-43-590 357), and by the Government of Perm Krai (Competition of Scientific Schools, International Research Teams competition).
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Russian Text © The Author(s), 2019, published in Zhurnal Organicheskoi Khimii, 2019, Vol. 55, No. 7, pp. 1024–1029.
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Antonov, D.I., Dmitriev, M.V. & Maslivets, A.N. Three-Component Spiro Heterocyclization of Pyrrolediones with Aminoindenones. Synthesis of Spiro[diindeno[1,2-b:2′,1′-e]pyridine-11,3′-pyrroles]. Russ J Org Chem 55, 933–937 (2019). https://doi.org/10.1134/S1070428019070029
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DOI: https://doi.org/10.1134/S1070428019070029