FIELD: chemistry.
SUBSTANCE: invention relates to oxazole pyrimidine compounds of formula in any of stereomeric forms thereof or a physiologically acceptable salt thereof, where A is O; X is (C1-C6)alkanediiyl oxy; R1 is (C1-C6)alkyl; R2 is phenylene, optionally substituted at one or two ring carbon atoms with identical or different R22; R3 is (C1-C6)alkyl, optionally substituted with 1-3 fluorine atoms, or (C3-C7) cycloalkyl-CuH2u- (u is selected from 1 and 2), or R3 is a residue of a saturated or unsaturated 4-10-member monocyclic or bicyclic ring containing 0, 1, 2 or 3 identical or different heteroatoms in the ring, selected from N, O and S, and is (C4-C6)cycloalkyl, indanyl, phenylene, naphthyl, isothiazolyl, thiadiazolyl, pyridyl, benzothiazolyl, quinolinyl, tetrahydrofuranyl, where the ring residue is optionally substituted at one or more ring carbon atoms with R31 substitutes; R4 is hydrogen; R22 is (C1-C4)alkyl; R31 is selected from a group consisting of a halogen and (C1-C4) alkyl, which is optionally substituted with 1-3 fluorine atoms, (C1-C4)alkyloxy, which is optionally substituted with 1-3 fluorine atoms, and (C1-C4)alkyl-S(O)m-, wherein (C1-C4)alkyl is optionally substituted with 1-3 fluorine atoms; m equals 0. The invention also relates to a pharmaceutical composition containing a compound of formula I, and to a method of producing compounds of formula I.
EFFECT: invention provides compounds of formula I, which are intended for EDG-1 receptor activation and wound healing.
17 cl, 2 tbl, 2 ex
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Authors
Dates
2015-08-20—Published
2011-01-12—Filed