ANALOGIFREMGANGSMAADE TIL FREMSTILLING AF TAUTOMERE AMINOSUBSTITUEREDE 4,5,6,7-TETRAHYDRO-1H-(ELLER 2H)-INDAZOLER ELLER SALTE DERAF

ANALOGIFREMGANGSMAADE TIL FREMSTILLING AF TAUTOMERE AMINOSUBSTITUEREDE 4,5,6,7-TETRAHYDRO-1H-(ELLER 2H)-INDAZOLER ELLER SALTE DERAF

Novel amino-substituted -4,5,6,7-tetrahydro-1H-(or 2H)-indazoles, useful as prolactin inhibitors and in treatment of Parkinson's Syndrome, are described herein. These compounds are prepared by reacting, by reductive alkylation with an aldehyde or by reacting with an alkyl halide or anhydride fo...

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Bibliographische Detailangaben
Hauptverfasser: KORNFELD EDMUND CARL, BACH NICHOLAS JAMES
Format: Patent
Sprache:dan
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CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
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Zusammenfassung:Novel amino-substituted -4,5,6,7-tetrahydro-1H-(or 2H)-indazoles, useful as prolactin inhibitors and in treatment of Parkinson's Syndrome, are described herein. These compounds are prepared by reacting, by reductive alkylation with an aldehyde or by reacting with an alkyl halide or anhydride followed by reduction, an 5(or 6)-amino-4,5,6,7-tetetrahydro-1H(or 2H)-indazole compound.