FIELD: chemistry.
SUBSTANCE: invention relates to novel compounds of formula I and formula II or pharmaceutically acceptable salts thereof, having the properties of a leucine repeat kinase inhibitor 2 (LRRK2, id est "Leucine Rich Repeat Kinase"). Compounds of formula I and formula II correspond to structures
or
In the compound of formula I, m is 0, 1 or 2; X is -NRa- or -O-, and Ra represents a hydrogen atom or C1-6alkyl; R1 is C1-6alkyl or C3-6cycloalkyl optionally substituted with a halogen atom, or, if X is NH, R1 is deuterated C3-6cycloalkyl; or R1 and Ra together with the atoms to which they are attached, can form a three-six-membered ring; R2 is a halogen atom, cyano or halo-C1-6alkyl; R3 is -OR4, a halogen atom or C1-6alkyl; R4 is a hydrogen atom, C1-6alkyl, halogen-C1-6alkyl, C3-6cycloalkyl or C3-6cycloalkyl-C1-6alkyl; R5 is a hydrogen atom or C1-6alkyl; R6 is a hydrogen atom, C1-6alkyl, hydroxy-C1-6alkyl, C3-6cycloalkyl-C1-6alkyl, optionally substituted with hydroxy, 5-6 membered heteroaryl or heterocyclyl with 1 to 2 nitrogen atoms as ring heteroatoms; where heteroaryl and heterocyclyl each may be optionally substituted with C1-6alkyl; or R5 and R6 together with the nitrogen atom to which they are attached, form a four-seven-membered ring, optionally including an additional heteroatom selected from O and N, and optionally substituted with one or two groups independently selected from the following groups: C1-6alkyl, C1-6alkoxy, halogen-C1-6alkoxy, C1-6alkoxy-C1-6alkyl, hydroxy-C1-6alkyl, halogen atom, C3-6cycloalkyl-C1-6alkyl and 4-6 membered heterocyclyl with 1 to 2 heteroatoms selected from N and O; or R5 and R6 together with the nitrogen atom to which they are attached, and an additional heteroatom O form a deuterated morpholino group; or hexahydro-pyrrolo [1,2-a]pyrazinyl, 8-oxa-3-aza-bicyclo[3.2.1]oct-3-yl, 2-oxa-5-aza-bicyclo[2.2.1]hept-5-yl, 1-oxa-6-aza-spiro[3.3]hept-6-yl or 2-oxa-6-aza-spiro[3.3]hept-6-yl; and R7 is a hydroxy group, a halogen atom, C1-6alkyl, C1-6alkoxy, halogen-C1-6alkyl or halogen-C1-6alkoxy; wherein said compound is selected from the group of compounds indicated in claim 1 of the invention. Preferably such a compound may be [4-(4-cyclopropylamino-5-trifluoromethyl-pyrimidin-2-ylamino)-2-fluoro-5-methoxy-phenyl]-morpholin-4-yl-methanone or [4-(4-cyclopropylamino-5-trifluoromethyl-pyrimidin-2-ylamino)-5-methoxy-2-methyl-phenyl]-morpholin-4-yl-methanone. In the compound of formula II, A is a five- or six-membered ring containing one or two heteroatoms, each independently selected from O; m is 0, 1 or 2; X is -NRa- or -O-, and Ra represents a hydrogen atom or C1-6alkyl; R1 is C1-6alkyl or C3-6cycloalkyl; or R1 and Ra together with the atoms to which they are attached, can form a three-six-membered ring; R2 is a halogen atom, cyano or halo-C1-6alkyl; R5 is a hydrogen atom or C1-6alkyl; R6 is a hydrogen atom, C1-6alkyl, hydroxy-C1-6alkyl, C3-6cycloalkyl-C1-6alkyl or heterocyclyl with 1 to 2 nitrogen atoms as heteroatoms in the ring, where heterocyclyl may be optionally substituted with C1-6alkyl; or R5 and R6 together with the nitrogen atom to which they are attached, form a four to six membered ring optionally including an additional heteroatom selected from O or N, and optionally substituted with one or two groups independently selected from the following groups: C1-6alkyl, C1-6alkoxy, halogen-C1-6alkoxy, C1-6alkoxy-C1-6alkyl, hydroxy-C1-6alkyl, halogen atom, C3-6cycloalkyl-C1-6alkyl and 4-6 membered heterocyclyl with 1 to 2 heteroatoms selected from N and O; or hexahydro-pyrrolo[1,2-a]pyrazinyl, 8-oxa-3-aza-bicyclo[3.2.1]oct-3-yl, 2-oxa-5-aza-bicyclo[2.2.1]hept-5-yl, 1-oxa-6-aza-spiro[3.3]hept-6-yl or 2-oxa-6-aza-spiro [3.3] hept-6-yl; and R7 is a halogen atom, C1-6alkyl, C1-6alkoxy, halogen-C1-6alkyl or halogen-C1-6alkoxy.
EFFECT: compounds can be used to treat Parkinson's disease mediated by the activity of said kinase.
11 cl, 6 tbl, 20 ex
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Authors
Dates
2018-07-13—Published
2012-11-28—Filed