FIELD: organic chemistry. SUBSTANCE: compound of formula (I) where R1 - hydrogen, R2 - hydrogen or hydroxy-group, or R1 and R2 together form the bond, R3 - hydrogen or benzyl, R4 - hydrogen or trifluoromethyl radical, Z = 0-2. Reagent 1: compound of formula (II) where R3 and Z - as indicated above, R5 - lower alkyl. Reagent 2: compound of formula (III) where R4 - as indicated above, Hal - halide. Synthesized compounds are inhibitors of aromatase. EFFECT: improved method of synthesis. 2 tbl
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METHOD FOR OBTAINING SUBSTITUTED IMIDAZOLE OR ITS NONTOXIC PHARMACEUTICALLY ACCEPTABLE ACID-ADDITIVE SALT | 0 |
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SUBSTITUTED EMIDAZOLES, METHODS OF PREPARATION THEREOF, PHARMACEUTICAL COMPOSITION BASED THEREON, AND METHOD OF MEDICAL TREATMENT | 1992 |
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METHOD FOR OBTAINING SUBSTITUTED IMIDAZOLE OR ITS NONTOXIC PHARMACEUTICALLY ACCEPTABLE ACID-ADDITIVE SALT | 0 |
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COMPOUNDS INHIBITING AROMATASE ACTIVITY SELECTIVELY, METHOD OF SYNTHESIS, PHARMACEUTICAL COMPOSITION | 1993 |
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METHOD OF SYNTHESIS OF SUBSTITUTED IMIDAZOLES OR THEIR NONTOXIC PHARMACEUTICALLY ACCEPTABLE ADDITIVE SALTS | 0 |
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SU1819263A3 |
Authors
Dates
1994-10-15—Published
1990-03-29—Filed