Abstract
Mono- and dibromo derivatives were obtained in the bromination of 4-(p-methoxyphenyl)-2,3-dihydro-1H-1, 5-benzodiazepin-2-one in media with different acidities with N-bromosuccinimide in carbon tetrachloride. The UV, PMR, and mass spectra of the compounds obtained are discussed.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 842–846, June, 1979.
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Avramenko, V.I., Sharbatyan, P.A., Solomko, Z.F. et al. Bromination of 4-(p-methoxyphenyl)-2,3-dihydro-1h-1, 5-benzodiazepin-2-one. Chem Heterocycl Compd 15, 691–694 (1979). https://doi.org/10.1007/BF00539511
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DOI: https://doi.org/10.1007/BF00539511