FIELD: organic chemistry.
SUBSTANCE: invention relates to a compound of formula (I)
or a pharmaceutically acceptable salt thereof, wherein R1 is cyclopropyl, C1-C4-alkyl or haloazetidinyl; R2 is cyclopropylmethoxy, C1-C4-alkoxy, haloC1-C4-alkoxy, halopyridinyl, alkylpyrazolyl or halopyrrolidinyl; provided that at least one of R1 and R2 is cyclopropyl or cyclopropylmethoxy; R3 is -C(O)-NH-C(R4R5)-R6, -C(O)-R7 or R8; R4 and R5 are independently selected from hydrogen, C1-C4-alkyl, C1-C4-cycloalkyl, C1-C4-cycloalkyl C1-C4-alkyl, C1-C4-alkylsulfonylC1-C4-alkyl and C1-C4-alkyloxetanil; or R4 and R5 together with the carbon atom to which they are bonded, form oxetanyl or dioxothetanyl; R6 represents aminocarbonyl, 5-methyl-1,2,4-oxadiazol-3-yl, hydroxyC1-C4-alkyl, thiazolyl, C1-C4-alkoxycarbonyl, carboxy, difluoroazetidinylcarbonyl, 5-amino-1, 2,4-oxadiazol-3-yl, C1-C4-alkylaminocarbonyl or aminocarbonyl C1-C4-alkyl; R7 is (aminocarbonyl)(difluoro)pyrrolidinyl or (aminocarbonyl)azaspiro[2.4]heptyl; R8 is 3-C1-C4-alkyl-1,2,4-oxadiazol-5-yl or 5-C1-C4-alkyl-1,2,4-oxadiazol-3-yl. Invention also relates to a pharmaceutical composition, use and to a method for activating cannabinoid receptors 2.
EFFECT: obtaining novel organic compounds which are selective agonists of cannabinoid receptors 2.
17 cl, 74 ex
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Authors
Dates
2020-07-31—Published
2016-12-06—Filed