ARYLMETHYLAZOLES AND THEIR SALTS, PROCESSES FOR THEIR PREPARATION, AGENTS WHICH CONTAIN THESE COMPOUNDS, AND THEIR USE

ARYLMETHYLAZOLES AND THEIR SALTS, PROCESSES FOR THEIR PREPARATION, AGENTS WHICH CONTAIN THESE COMPOUNDS, AND THEIR USE

Arylmethylazoles of the formula I in which Aryl is (substituted) phenyl or naphthyl; Z is CH or N; R1 and Q are H or alkyl; R2 is H, alk(en)yl or alkynyl; R3 and R4 are H, alkyl or other hydrocarbons; or R3 and R4 together are a -(CH2)2-11 chain or a bridged -(CH2)4-5 chain, and their acid addition...

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Bibliographische Detailangaben
Hauptverfasser: SCHACHT, ULRICH, ALPERMANN, HANS G, GERHARDS, HERMANN J, SIEGEL, HERBERT, LEVEN, MARGRET, USINGER, PATRICIA, DITTMAR, WALTER, RAETHER, WOLFGANG, KAMPE, KLAUS-DIETER, SACHSE, BURKHARD
Format: Patent
Sprache:eng ; fre
Schlagworte:
CHEMISTRY
HETEROCYCLIC COMPOUNDS
HUMAN NECESSITIES
HYGIENE
MEDICAL OR VETERINARY SCIENCE
METALLURGY
ORGANIC CHEMISTRY
PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
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Beschreibung
Zusammenfassung:Arylmethylazoles of the formula I in which Aryl is (substituted) phenyl or naphthyl; Z is CH or N; R1 and Q are H or alkyl; R2 is H, alk(en)yl or alkynyl; R3 and R4 are H, alkyl or other hydrocarbons; or R3 and R4 together are a -(CH2)2-11 chain or a bridged -(CH2)4-5 chain, and their acid addition salts, stereoisomers and optically active enantiomers possess outstanding antimycotic and antidepressant activity. The compounds of the Formula I are obtained, inter alia, from arylmethylazoles II II which are reacted with a strong base and then with a carbonyl compound III 0=CR3R4; thereafter, the product is reacted with the protic acid or with an alkyl halide IV R2Hal. If desired, the products are converted to the acid addition salts, or the stereoisomers or optically active enantiomers are resolved.