发明名称 Pyrazole aminopyrimidine derivatives as LRRK2 modulators
摘要 Compounds of the formula I:;or pharmaceutically acceptable salts thereof,wherein X, R1, R2, R3, R4 and R5 are as defined herein. Also disclosed are methods of making the compounds and using the compounds for treatment of diseases associated with LRRK2 receptor, such as Parkinson's disease.
申请公布号 US8815882(B2) 申请公布日期 2014.08.26
申请号 US201113292668 申请日期 2011.11.09
申请人 Genentech, Inc. 发明人 Baker-Glenn Charles;Burdick Daniel Jon;Chambers Mark;Chan Bryan K.;Chen Huifen;Estrada Anthony;Sweeney Zachary Kevin
分类号 A01N43/54;A61K31/505 主分类号 A01N43/54
代理机构 代理人 Hall Robert C.
主权项 1. A compound of the formula I:or a pharmaceutically acceptable salt thereof,wherein: X is: —NRa—; or —O— wherein Ra is hydrogen or C1-6alkyl; R1 is: C1-6alkyl; C2-6alkenyl; C2-6alkynyl; halo-C1-6alkyl; C1-6alkoxy-C1-6alkyl; hydroxy-C1-6alkyl; amino-C1-6alkyl; C1-6alkylsulfonyl-C1-6alkyl; C3-6cycloalkyl optionally substituted one or more times with C1-6alkyl; C3-6cycloalkyl-C1-6alkyl wherein the C3-6cycloalkyl portion is optionally substituted one or more times with C1-6alkyl; heterocyclyl optionally substituted one or more times with R7; or heterocyclyl-C1-6alkyl optionally substituted one or more times with R7, wherein the heterocyclyl is piperidinyl, piperazinyl, morpholinyl, tetrahydropyranyl, pyrrolidinyl, tetrahydrofuranyl or oxetanyl; or X and R1 together form C1-6alkyl; C1-6alkoxy-C1-6alkyl; C3-6cycloalkyl optionally substituted one or more times with R6; or C3-6cycloalkyl-C1-6alkyl wherein the C3-6cycloalkyl portion is optionally substituted one or more times with R6; or R1 and Ra together with the atoms to which they are attached may form a three- to six-membered ring optionally substituted one or more times with R7; R2 is: halo; cyano; or halo-C1-6alkyl; R3 is: hydrogen; C1-6alkyl; halo-C1-6alkyl; C2-6alkenyl; C2-6alkynyl; hydroxy-C1-6alkyl; C1-6alkoxy-C1-6alkyl; cyano-C1-6alkyl; C1-6alkylsulfonyl; C1-6alkylsulfonylC1-6alkyl; amino-C1-6alkyl; C3-6cycloalkyl optionally substituted one or more times with R6; C3-6cycloalkyl-C1-6alkyl wherein the C3-6cycloalkyl portion is optionally substituted one or more times with R6; C3-6cycloalkyl-sulfonyl wherein the C3-6cycloalkyl portion is optionally substituted one or more times with R6; heterocyclyl optionally substituted one or more times with R7; heterocyclyl-C1-6alkyl wherein the heterocyclyl portion is optionally substituted one or more times with R7, wherein the heterocyclyl is piperidinyl, pyrrolidinyl, oxetanyl, tetrahydropyranyl, tetrahydrofuranyl, azetidinyl, [1,3]dioxolanyl or tetrahydrothiopyranyl; aryl optionally substituted one or more times with R8; aryl-C1-6alkyl wherein the aryl portion is optionally substituted one or more times with R8; heteroaryl optionally substituted one or more times with R8; heteroaryl-C1-6alkyl wherein the heteroaryl portion is optionally substituted one or more times with R8; or —Y—C(O)—Rd; Y is C2-6alkylene or a bond; Rd is C1-6alkyl, C1-6alkoxy, amino, C1-6alkyl-amino, di-C1-6alkyl-amino, halo-C1-6alkyl-amino, di-halo-C1-6alkyl-amino, halo-C1-6alkyl, hydroxy-C1-6alkyl, hydroxy, C1-6alkoxy-C1-6alkyl, cyano-C1-6alkyl, C1-6alkylsulfonylC1-6alkyl, amino-C1-6alkyl, C3-6cycloalkyl optionally substituted one or more times with R6, C3-6cycloalkyl-C1-6alkyl wherein the C3-6cycloalkyl portion is optionally substituted one or more times with R6-heterocyclyl optionally substituted one or more times with R7, or heterocyclyl-C1-6alkyl wherein the heterocyclyl portion is optionally substituted one or more times with R7, wherein the heterocyclyl is piperidinyl, piperazinyl, morpholinyl, tetrahydropyranyl, pyrrolidinyl, azetidinyl, tetrahydrofuranyl or oxetanyl; R4 is: chloro; or methyl; R5 is: hydrogen; or C1-6alkyl; each R6 is independently: C1-6alkyl; halo-C1-6alkyl; C1-6alkoxy; oxo; cyano; halo; or Y—C(O)—Rd; each R7 is independently: C1-6alkyl; halo-C1-6alkyl; halo; oxo; C1-6alkoxy; C1-6alkylsulfonyl; C1-6 alkoxy-C1-6alkyl; cyano; —Y—C(O)—Rd; heterocyclyl; heterocyclyl-C1-6alkyl; C3-6cycloalkyl; C3-6cycloalkyl-C1-6alkyl; or C3-6cycloalkylsulfonyl, wherein the heterocyclyl is piperidinyl, pyrrolidinyl, oxetanyl, tetrahydropyranyl, tetrahydrofuranyl, azetidinyl, [1,3]dioxolanyl or tetrahydrothiopyranyl; and each R8 is independently: oxo; C1-6alkyl; halo-C1-6alkyl; halo; C1-6alkyl-sulfonyl; C1-6alkoxy; C1-6alkoxy-C1-6alkyl; cyano; heterocyclyl; heterocyclyl-C1-6 alkyl; —Y—C(O)—Rd; C3-6cycloalkyl, C3-6cycloalkyl-C1-6alkyl, or C3-6cycloalkyl-sulfonyl, wherein the heterocyclyl moiety is piperidinyl, piperazinyl, morpholinyl, thiomorpholinyl, pyrrolidinyl, oxetanyl, tetrahydropyranyl, tetrahydrofuranyl, azetidinyl, [1,3]dioxolanyl or tetrahydrothiopyranyl.
地址 South San Francisco CA US