FIELD: chemistry.
SUBSTANCE: present invention relates to organic chemistry and specifically to compounds of formula I or pharmaceutically acceptable salts thereof, where W is where each R4 independently denotes H or CN; R2 denotes a cycloalkyl which can be independently substituted with two of the following substitutes: C(1-3)alkyl; Z denotes H; J denotes CH or N; X denotes or ; where R1 denotes -ORa, -CN, -NA1A2, -SO2CH3, -COORa, -CO2CH3, -CH2-NA1A2, -CONA1A2, -CH2ORa, -NHCH2CH2ORa, -OC(1-4)alkylNA1A2, OCH2CO2Ra and tetrazolyl; Rz and Ry independently denotes H or -C(1-4)alkyl, where both Rz may have syn or anti stereochemistry; alternatively both Rz in syn interaction may be taken together to form -(CH2)n-, where n equals 2; R3 denotes C(1-3)alkyl-CF3 or -COCH3; A1 denotes H or -C(1-4)alkyl; A2 denotes H or -C(1-4)alkyl; alternatively, A1 and A may be taken together with a nitrogen atom with which they are bonded to form a heterocyclic ring selected from: , where Ra denotes H or C(1-4)alkyl; Rbb denotes H, -C(1-4)alkyl, and -CH2CO2H, where cycloalkyl relates to a partially unsaturated ring with 6 carbon atoms. The invention also relates to specific compounds of formula I, a pharmaceutical composition based on the compound of formula I and methods of treating inflammation and autoimmune diseases.
EFFECT: novel compounds of formula I which are useful as c-fms inhibitors are obtained.
10 cl, 2 tbl, 44 ex
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Authors
Dates
2013-02-20—Published
2007-04-18—Filed