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Antibiotic derivatives of streptomycin

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1. PROCESS FOR PRODUCING ANTIBIOTIC AGENTS, WHICH RETAIN THEIR ANTIBIOTIC ACTIVITY IN THE PRESENCE OF CYSTEINE AND HAVE THE FUNDAMENTAL CHEMICAL STRUCTURE OF STREPTOMYCIN EXCEPT THAT THE STREPTOSE CARBONYL GROUP IS REPLACED BY AN AMINOMETHYLENE GROUP, THAT COMPRISES TREATING A MATERICAL CHOSEN FORM THE GROUP CONSISTING OF STREPTOMYCIN AND ITS SALTS, WITH A COMPOUND CHOSEN FROM THE GROUP CONSISTING OF HYDROXYL AMINE AND ARYL HYDRAZINES, WHEREBY THE OXYGEN ATOM OF THE CARBONYL GROUP IS REPLACED WITH A SUBSTITUTED NITROGEN ATOM CONNECTED BY A DOUBLE VALENCE BOND TO THE CARBON ATOM; CATALYTICALLY HYDROGENATING THIS SUBSTANCE TO CONVERT THE SAID SUBSTITUTED NITROGEN ATOM TO AN AMINO GROUP BY DIRECT REACTION WITH HYDROGEN, IN THE PRESENCE OF A HYDROGENATION CATALYST OF THE RANEY-NICKEL TYPE, WHILE IN A LIQUID SOLVENT MEDIUM AND AT A HYDROGEN ION CONCENTRATION OF APPROXIMATELY PB 7.
2. AN ANTIBIOTIC AGENT, ANTAGONISTIC TO PATHOGENIC MICRO-ORGANISMS, HAVING ANTIBIOTIC ACTIVITY SIMILAR TO THAT CHARACTERISTIC OF STREPTOMYCIN BUT DIFFERING THEREFROM IN RETAINING ITS ACTIVITY IN THE PRESENCE OF CYSTERINE, HAVING THE FUNDAMENTAL CHEMICAL STRUCTURE REPRESENTED BY THE FORMULA:
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