Abstract
The reactions of 2-(2-aminophenyl)benzimidazole with substituted isatins afforded the corresponding 5,6-dihydrospiro(benz[4,5]imidazo[1,2-c]quinazoline-6,3′indolin)-2′-ones. The spirocyclic structure of the reaction products was established by NMR spectroscopy and X ray diffraction analysis.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1987–1989, September, 2004.
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Morozov, P.G., Kurbatov, S.V., Dolgushin, F.M. et al. Synthesis and structures of substituted 5,6-dihydro-spiro(benz[4,5]imidazo[1,2-c]quinazoline-6,3′-indolin)-2′-ones. Russ Chem Bull 53, 2071–2074 (2004). https://doi.org/10.1007/s11172-005-0074-1
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DOI: https://doi.org/10.1007/s11172-005-0074-1