BENZO-[F]-QUINOLINONES, METHOD OF INHIBITION, METHOD OF SYNTHESIS OF BENZO-[F]-QUINOLINONES, METHOD OF RACEMATES SPLITTING AND DI-P-TOLUOYL-(D)- OR (L)-TARTARIC ACID SALT Russian patent published in 1999 - IPC

Abstract RU 2126386 C1

FIELD: organic chemistry, medicine. SUBSTANCE: invention relates to benzo-[a] -quinolinone of the formula (I) where R is H, alkyl or phenalkyl; Z and Z' - are H, alkyl or one of Z and Z' with R5 forms a bond carbon-carbon Y is H or methyl or with SSS forms a band carbon-carbon; R1 is H or forms a bond carbon-carbon with one of Y or R3; R2 is H or C1-4 alkyl; R3 is H or R1 forms a bond carbon-carbon; R4 is H or with R5 forms a bond carbon-carbon; R5 is H or with one of Z or Z' forms a bond carbon-carbon; n = 1 or 2; X is H, halogen, NO2, cyano-group, CF3, C1-6-alkyl, alkoxy-, carboxy-, alkoxycarbonyl-, amino-, amido-group or a group -A-O-R6 where A is C1-6-alkylene, C2-6-alkenyl or C2-6-alkynylene; R6 - halogen, hydroxy, alkylamido-group or its pharmaceutically acceptable salt. Compounds of the formula (I) are selective steroid inhibitors of 5α--reductase showing strong effect and can be used for treatment of patients with prostate benignity tumors, alopecia, acnes and seborrhea in males. EFFECT: improved method of synthesis, enhanced effectiveness of compounds. 19 cl, 1 tbl, 69 ex

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RU 2 126 386 C1

Authors

Dzhejms Ehdmund Odia

Kennet Stiven Kherch

Charl'Z Dehvid Dzhons

Dehvid Ehrnst Lokhorn

Loretta Ehms Makkuajd

Dates

1999-02-20Published

1992-08-20Filed