Zusammenfassung
1-Phenyl-1,2,3,4-tetrahydrochinolinderivate mit Substituenten (Methyl, Äthyl, Chlor, Methoxyl) in Stellung 6 und/oder 4′ wurden dargestellt: Cyclisierung der entsprechenden β-(Diphenylamin-N)-propionsäuren lieferte die 4-Oxoverbindungen. Die 4-Aminoderivate wurden durch Reduktion der 4-Hydroximinoverbindungen hergestellt.
Abstract
1-Phenyl-1,2,3,4-tetrahydroquinoline derivatives with substituents (methyl, ethyl, chloro, methoxyl) in position 6 and/or 4′ were synthesized: cyclization of the corresponding diphenylaminopropionic acids yielded the 4-oxo compounds. The 4-amino derivatives were prepared by reduction of the 4-hydroximino compounds.
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Hromatka, O., Sauter, F., Knollmüller, M. et al. Synthesen von Derivaten des 1-Phenyl-1,2,3,4-tetrahydrochinolins. Monatshefte für Chemie 97, 1763–1770 (1966). https://doi.org/10.1007/BF00901453
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DOI: https://doi.org/10.1007/BF00901453