Abstract
N-Alkyl substituted tetrahydropyrrolo[3,2-c]pyridines have been obtained by alkylation of 4,5,6,7-tetrahydro-4,-5, 7-trimethylpyrrolo[3,2-c]pyridine and its 2-formyl derivative chloroalkyldimethylamines, acrylonitrile, methyl acetylenedicarboxylate and dichloroethane. 2-Formyl substituted tetrahydropyrrolo[3,2-c]pyridine has been reduced with sodium borohydride and condensed with monoethanolamine and hydroxylamine. The stereochemistry of the products has been studied by 1H NMR spectroscopy.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 681–687, May, 1993.
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Varlamov, A.V., Borisova, T.N., Aliev, A.É. et al. Chemical reactions of 4,5,6,7-tetrahydro-4,5,7-trimethylpyrrolo[3,2-c]pyridine and its 2-formyl derivative. Chem Heterocycl Compd 29, 582–587 (1993). https://doi.org/10.1007/BF00534474
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DOI: https://doi.org/10.1007/BF00534474