Abstract
1 is synthesized by reaction of cinchomeronic anhydride with ethyl acetoacetate and triethylamine in acetic anhydride. Its structure is discussed by means of IR- and1H-NMR-spectrum. By reaction of1 with SOCl2 3 is formed, which is converted with ethyl sarcosinate to4. The structure of4 is confirmed by chemical proof.Dieckmann cyclisation of4 gives the title compound7.
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Literatur
1. Mitt.:D. Binder, Mh. Chem.105, 179 (1974).
L. J. Bellamy, Ultrarot-Spektrum und chemische Konstitution, 2. Aufl., S. 202. Dr. D. Steinkopff-Verlag. 1966.
2. Mitt.:D. Binder, Mh. Chem.105, 196 (1974).
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Binder, D. Pyrindinchemie, 3. Mitt.: Über die Synthese des 3-Hydroxy-1-methyl-4-oxo-1,4-dihydro-pyrrolo[2′,3′:3,4]cyclopenta[1,2-c]pyridin-2-carbonsäureäthylesters. Ein Vertreter eines neuen heterocyclischen Ringsystems. Monatshefte für Chemie 105, 203–208 (1974). https://doi.org/10.1007/BF00911307
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DOI: https://doi.org/10.1007/BF00911307