FIELD: biotechnologies.
SUBSTANCE: invention relates to new derivatives of 4-aminopyrimidine, having antagonistic activity in respect to the receptor H4. In the formula : R1 is selected from C1-8alkyl, C3-8cycloalkyl-C0-6alkyl, aryl-C1-6alkyl, the group of the formula R2 and R3 together with the atom N, with which they are linked, creating the saturated heterocyclic group, which may be a 4-7-member monocyclic or 9-member condensed bycyclic one, where the specified heterocyclic group may contain up to two atoms N and does not contain any other heteroatoms, and may be unnecessarily substituted with one or more substitutes, independently selected from C1-4alkyl and NRaRb, provided that if the heterocyclic group either contains 2 atoms N and is not substituted with the group NRaRb, or comprises 1 atom N and is substituted with one group NRaRb; or R2 is H, and R3 is pyrrolidinyl substituted with C1-4alkyl group; where Ra is H or C1-4alkyl; Rb is H or C1-4alkyl; R4 and R5 is H; R6 is aryl group; n is equal to 1; and aryl is phenyl group, unnecessarily substituted with halogen. The invention also relates to a pharmaceutical composition containing the specified compounds, to application of compounds for production of a medicinal agent for treatment of such diseases as an allergic, immunological or inflammatory diseases or pain, and also to a method for production of the specified compounds.
EFFECT: higher efficiency of application of compounds in treatment of diseases.
34 cl, 30 ex
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Authors
Dates
2013-08-10—Published
2008-12-18—Filed