FIELD: medical chemistry.
SUBSTANCE: present invention relates to a compound of formula (I) or a pharmaceutically acceptable salt or prodrug thereof. In formula (I): X is CH; Y is 1 O; Z is C(R6)2; m is 0 or 1; L is -C (R7)2- or n is 0, 1 or 2; each R1 is independently C1-3 alkyl or C1-3 haloalkyl; R2 and R3 each independently represents a halogen; R4 is hydrogen; R5 is hydrogen; two R6 and carbon atoms to which they are bonded together form C3-8 cycloalkyl or 4–10-membered heterocycloalkyl; where 4–10-membered heterocycloalkyl includes 1 ring-forming heteroatom O; each R7 is independently hydrogen, halogen, C1-8 alkyl, 3–10 membered heterocycloalkyl or 3–10 membered heterocycloalkyl, substituted with C1-4 alkyl or morpholinyl; wherein said 3–10-membered heterocycloalkyl independently includes 1 to 2 ring-forming heteroatoms, and each of said heteroatoms is independently N, O. Also disclosed is a pharmaceutical composition and a pharmaceutical preparation containing said compound, and use thereof.
EFFECT: disclosed compound can be used as an FGFR4 inhibitor for preventing and/or treating diseases mediated, at least partially, by FGFR4.
11 cl, 2 tbl, 19 ex
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Authors
Dates
2024-10-01—Published
2021-11-10—Filed