FIELD: organic chemistry, pharmacy. SUBSTANCE: invention relates to derivatives of pyrazole of the formula (I) where X1 means group -NRR1R2 or group -OR2; g2-g6 are similar or distinct and mean independently each of other hydrogen, halogen atom, C1-4-alkyl, C1-4-alkoxyl-group, trifluoromethyl-group or C1-4-alkylthio-group; w2-w6 are similar or distinct and mean independently each of other hydrogen, halogen atom, C1-4-alkyl, C1-4-alkoxyl or trifluoromethyl-group under condition that at least one of substituents g2-g6 and one of substituents w2-w6 are distinct from hydrogen atom; R1 means hydrogen atom or C1-4- alkyl; R2 is nonaromatic unsubstituted C3-15-carbocyclic radical or that mono- or multisubstituted with C1-4-alkyl; R3 is hydrogen atom or group CH2-R6;; each of R4 and R5 means independently hydrogen atom or C1-4-alkyl; or R4 means hydrogen atom and R5 and w6 in common form ethylene radical; R6 means hydrogen or if substituents g2, g3, g4, g5 and/or g6/ are distinct from C1-4-alkyl then R6 means hydrogen atom, C1-4-alkyl or C1-5-alkoxyl, and to their salts. Invention relates to also method of synthesis of derivatives of pyrazole of the formula (I) and pharmaceutical composition containing thereof. New synthesized compounds are antagonists of CB2 receptors and pharmaceutical composition has affinity to CB2 receptors and they can be used for treatment of patients with autoimmune diseases. EFFECT: new compounds indicated above, improved method of synthesis, valuable medicinal and pharmacological properties. 17 cl, 2 tbl, 59 ex
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