Summary
The reaction between benzoquinone and two or more mols ethylenimine yields a white insoluble compound which is the internal salt of 2,5-bis-ethylenimino-hydroquinone, an unusual formation not yet described in the literature. C-Methyl-ethylenimine forms a similar hydroquinone salt, whilst other cyclic or non cyclic amines, such as piperidine, pyrrolidine, trimethylenimine, dimethylamine and C,C-dimethyl-ethylenimine give 2,5-disubstituted benzoquinones. According to the findings ofLoustalot, Schär andMeier 2,5-Bisethylenimino-hydroquinone has proved to be of remarkable efficacy in seven kinds of transplantable tumors. It would seem, therefore, that this compound has, both chemically and biologically, interesting qualities.
References
G. Domagk, S. Petersen undW. Gauss, Z. Krebsforschung59, 617 (1954).
P. Loustalot, B. Schär undR. Meier, vgl. die nachfolgende Arbeit, Exper.11, 186 (1955).
Vgl. die Zusammenfassung beiM. Martynoff undG. Tsatsas, Bull. Soc. Chim. Fr.14, 52 (1947), undC. J. Cavallito, A. E. Soria undJ. O. Hoppe, J. Amer. Chem. Soc.72, 2661 (1950).
B. Lachowicz, Mh. Chem.9, 506 (1888).
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Marxer, A. Über ein carcinostatisch wirksames Hydrochinonderivat. Experientia 11, 184–186 (1955). https://doi.org/10.1007/BF02161308
Published:
Issue Date:
DOI: https://doi.org/10.1007/BF02161308