FIELD: pharmacology.
SUBSTANCE: invention relates to a compound of formula (Ic) or any of its pharmaceutically acceptable salts that can be used to treat and/or prevent RNA viral infection caused by an RNA virus belonging to group IV or V of the Baltimore virus classification selected from RSV (respiratory syncytial virus) and chikungunya viruses. In the compound of the formula (Ic), the ring and the ring both represent a phenylene group, or the ring is a pyridylene group, and the ring is a phenylene group; Z” represents –CH2– or –CO–; Rg is hydrogen and Rh is hydrogen or (C1–C4)alkyl; X2 represents –CO–NRk–, where Rk is hydrogen or methyl; –OCH2–, –CH(OH)–, -NH CO–, –O–, –O–(CH2)s–O–, where s is 2 or 3, –CO–, –SO2–, 5-membered heteroaromatic ring containing 1, 2, 3 or 4 heteroatoms, such as triazole, imidazole, tetrazole or oxadiazole, –NH–SO2–, –NH– or –SO2–NH–; n is 0, 1, 2 or 3, m and m’ are independently equal to 0, 1 or 2; Y2 is hydrogen, halogen, hydroxyl group, (C1–C4)alkoxy, etc.; R is (C1–C4)alkyl, (C3-C6)cycloalkyl, halogen; R’ represents (C1–C4)alkyl, optionally interrupted by –SO2– or –SO–, (C3-C6)cycloalkyl or trifluoromethyl group. The invention also relates to the use of a compound of the formula (Ic) for the treatment and/or prevention of the above-mentioned RNA viral infections.
EFFECT: invention also relates to a pharmaceutical composition containing the specified compound and a synthesis method for the production of a compound of the formula (Ic).
9 cl, 5 tbl, 7 ex
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Authors
Dates
2023-02-28—Published
2019-07-09—Filed