FIELD: chemistry.
SUBSTANCE: invention relates to a compound of general formula (I) or its mesomer, racemate, enantiomer or diastereomer or mixture thereof, or its pharmaceutically acceptable salt, which have the ability to modulate oestrogen receptors. In formula (I), R1a and R1b are identical or different and each is independently selected from the group consisting of a H atom, a deuterium atom, a halogen and a C1-6alkyl; ring A is 4–5 membered heterocyclyl containing 1 heteroatom selected from N; Z is selected from a group consisting of an O atom and NR7; all G1, G2, G3 and G4 are CR8 or one of G1, G2, G3 and G4 is a N atom, and the remaining ones are CR8; R2 is a hydrogen atom; R3 is a hydrogen atom; R4 is C1-6alkyl; R5 is C1-6alkyl, where said C1-6alkyl is substituted with one or more substitutes selected from the group consisting of halogen, hydroxy and C1-6hydroxyalkyl; R6 are identical or different and each is independently selected from the group consisting of a hydrogen atom and C1-6haloalkyl; R7 is a hydrogen atom; R8 are identical or different and each is independently selected from the group consisting of a hydrogen atom and a halogen; n is 1 or 2; s is 0, 1 or 2 and p is 0, 1 or 2. Invention also relates to methods of producing a compound of formula (I), intermediate compounds, a pharmaceutical composition containing a compound of general formula (I), and embodiments of its use for preventing and/or treating a disease or condition mediated by or dependent on an oestrogen receptor.
EFFECT: compounds can be used to prevent and/or treat a disease or condition mediated by an oestrogen receptor or dependent on it.
40 cl, 9 tbl, 21 ex
Authors
Dates
2024-11-13—Published
2021-01-08—Filed