FIELD: pharmaceuticals.
SUBSTANCE: invention relates to compounds of formula (I) and use thereof for detecting or visualizing CB2 receptors. In formula (I), R1 is a ring selected from phenyl and [1,2,5]oxadiazolyl, where said ring is substituted with one substitute selected from halosulphonyl, halosulphonyl-C1-8-alkyl, isothiocyanato-C1-8-alkyl, isothiocyanato, amino-C1-8-alkyldisulfanyl-C1-8-alkyl, hydroxy-C1-8-alkylsulphanyl-C1-8-alkyl, hydroxy-C1-8-alkyl disulphanyl, amino-C1-8-alkyl disulphanyl, halogen, C1-8-alkyl, pyridinyl disulphanyl-C1-8-alkyl, benzotriazolylsulfonyl-C1-8-alkyl, dihydroxy-C1-8-alkylsulphanyl-C1-8-alkyl and pyridinylsulphanyl and optionally further substituted with cyano; R2 and R3 are independently selected from hydrogen, hydroxyl, halogen, thiohydroxyl, azido, isothiocyanato and C1-8-alkyldisulfanyl; provided that at least one of R1, R2 and R3 is a group containing sulphonyl, isothiocyanato, disulphanyl, thiohydroxyl or azido; R4 is C1-8-alkyl or phenyl-di-halogen-C-1-8-alkyl; and n is 0 or 1. Invention also relates to a pharmaceutical composition for modulating CB2 receptors containing an effective amount of said compound of formula (I) and a therapeutically inert carrier.
EFFECT: disclosed are derivatives of [1,2,3]triazolo[4,5-d]pyrimidine with affinity for type 2 cannabinoid receptors.
12 cl, 39 ex
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Authors
Dates
2021-01-27—Published
2017-06-20—Filed