Abstract
4-(4-Aminophenylamino)-2,2,6,6-tetramethylpiperidine was synthesized by alkylation of 4-aminotriacetoneamine with 4-chloronitrobenzene, followed by hydrogenation of the nitro derivative. Its reactions with acrylic, methacrylic, and itaconic acids were carried out. Transformations of the N-substituted amino acids to derivatives of 2-pyrrolidinone and dihydropyrimidinedione were studied.
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Additional information
Kaunas Technological University, Kaunas LT-3028. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 629–631, May, 1997.
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Mitskyavichyus, V., Beresnyavichyus, Z. Some derivatives of 4-(4-aminophenylamino)-2,2,6,6-tetramethylpiperidine. Chem Heterocycl Compd 33, 543–545 (1997). https://doi.org/10.1007/BF02291936
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DOI: https://doi.org/10.1007/BF02291936