Abstract
9-Substituted 5,6-dihydro-4H-imidazo[4,5,1-i,j]quinolines were synthesized and aminated by the action of sodium amide and hydroxylated by fusing with potassium hydroxide. The mononitro and dinitro compounds of some 5,6-dihydro-4H-imidazo[4,5,1-i,j]quinoline deivatives and the corresponding amino and diamino compounds were obtained. The latter react with nitric or formic acids to form a new heterocyclic ring.
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See [1] for communication II.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 242–246, February, 1972.
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Simonov, A.M., Poludnenko, V.G. 5,6-Dihydro-4H-imidazo[4,5,1-i,j]quinoline derivatives. Chem Heterocycl Compd 8, 218–222 (1972). https://doi.org/10.1007/BF00472363
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DOI: https://doi.org/10.1007/BF00472363