发明名称 CATHEPSIN CYSTEINE PROTEASE INHIBITORS
摘要 This invention relates to a novel class of compounds which are cysteine protease inhibitors, including but not limited to, inhibitors of cathepsins K, L, S and B. These compounds are useful for treating diseases in which inhibition of bone resorption is indicated, such as osteoporosis.
申请公布号 US2014256743(A1) 申请公布日期 2014.09.11
申请号 US201414282395 申请日期 2014.05.20
申请人 Merck Frosst Canada Ltd. ;Axys Pharmaceuticals, Inc. 发明人 Bayly Christopher I.;Black Cameron;Leger Serge;Li Chun Sing;McKay Dan;Mellon Christophe;Gauthier Jacques Yves;Truong Vouy-Linh;Lau Cheuk;Therien Michel;Green Michael J.;Hirschbein Bernard L.;Janc James William;Palmer James T.;Baskaran Chitra I.
分类号 C07C237/20;C07D295/155;A61K31/495;C07C317/32;C07D213/57;A61K31/4174;C07C311/37;A61K31/18;A61K31/44;C07D277/30;A61K31/426;C07D233/64;A61K31/165;A61K31/4418 主分类号 C07C237/20
代理机构 代理人
主权项 1. The present invention relates to compounds of the following chemical formula: wherein R1 is hydrogen, C1-6 alkyl or C2-6 alkenyl wherein said alkyl and alkenyl groups are optionally substituted with one to six halo, C3-6 cycloalkyl, —SR9, —SR12, —SOR9, —SOR12, —SO2R9, —SO2R12, —SO2CH(R12)(R11), —OR12, —OR9, —N(R12)2, aryl, heteroaryl or heterocyclyl wherein said aryl, heteroaryl and heterocyclyl groups are optionally substituted with one or two substitutents independently selected from C1-6 alkyl, halo, hydroxyalkyl, hydroxy, alkoxy or keto; R2 is hydrogen, C1-6 alkyl or C2-6 alkenyl wherein said alkyl and alkenyl groups are optionally substituted with one to six halo, C3-6 cycloalkyl, —SR9, —SR12, —SOR9, —SOR12, —SO2R9, —SO2R12, —SO2CH(R12)(R11), —OR12, —OR9, —N(R12)2, aryl, heteroaryl or heterocyclyl wherein said aryl, heteroaryl and heterocyclyl groups are optionally substituted with one or two substitutents independently selected from C1-6 alkyl, halo, hydroxyalkyl, hydroxy, alkoxy or keto; or R1 and R2 can be taken together with the carbon atom to which they are attached to form a C3-8 cycloalkyl or heterocyclyl ring wherein said ring system is optionally substituted with one or two substituents independently selected from C1-6 alkyl, hydroxyalkyl, haloalkyl, or halo; R3 is hydrogen, C1-6 alkyl or C2-6 alkenyl wherein said alkyl and alkenyl groups are optionally substituted with C3-6 cycloalkyl or one to six halo; R4 is hydrogen, C1-6 alkyl or C2-6 alkenyl wherein said alkyl and alkenyl groups are optionally substituted with C3-6 cycloalkyl or one to six halo; or R3 and R4 can be taken together with the carbon atom to which they are attached to form a C3-8 cycloalkyl ring, C5-8 cycloalkenyl ring, or five to seven membered heterocyclyl wherein said cycloalkyl, cycloalkenyl and heterocyclyl groups are optionally substituted with one or two substitutents independently selected from C1-6 alkyl, halo, hydroxyalkyl, hydroxy, alkoxy or keto; R5 is selected from hydrogen or C1-6 alkyl substituted with 1-6 halo; R6 is aryl, heteroaryl, C1-6 haloalkyl, arylalkyl or heteroarylalkyl, wherein said aryl, heteroaryl, arylalkyl and heteroarylalkyl groups are optionally substituted with one, two, or three substituents independently selected from halo, C1-6 alkyl, C1-6 haloalkyl, C3-6 cycloalkyl, haloalkoxy, —SR9, —SR12, —SOR9, —SOR12, —SO2R9, —SO2R12, —SO2CH(R12)(R11), —OR12, —N(R10)(R11), cyano, or aryl which is optionally substituted with —SO2R12; each D is independently C1-3 alkyl, C2-3 alkenyl, C2-3 alkynyl, aryl, heteroaryl, C3-8 cycloalkyl or heterocyclyl wherein each said aryl, heteroaryl, cycloalkyl and heterocyclyl groups, which may be monocyclic or bicyclic, is optionally substituted on either the carbon or the heteroatom with one to five substituents independently selected from C1-6 alkyl, haloalkyl, halo, keto, alkoxy, —SR9, —SR12, —OR9, —OR12, N(R12)2, —SO2R9, or —SO2R10; R7 is hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, C1-6 alkyloxy, halo, nitro, cyano, aryl, heteroaryl, C3-8 cycloalkyl, heterocyclyl, —C(O)OR10, —C(O)OSi[CH(CH3)2]3, —OR9, —ORM, —C(O)R10, —R10C(O)R9, —C(O)R9, —C(O)N(Ra)(Rb), —C(O)N(R12)(R12), —C(O)N(R10)(R11), —C(R10)(R11)OH, —SR12, —SR9, —R10SR9, —R9, —C(R9)3, —C(R10)(R11)N(R9)2, —NR10C(O)NR10S(O)2R9, —SO2R12, —SO(R12), —SO2R9, —SOmN(Rc)(Rd), —SOmCH(R10)(R11), —SO2N(R10)C(O)(R12), —SO2(R10)C(O)N(R12)2, —OSO2R10, —N(R10)(R11), —N(R10)C(O)N(R10)(R9), N(R10)CO(R9), —N(R10)C(O)R10, —N(R10)C(O)OR10, —N(R10)SO2(R10), —C(R10)(R11)NR10C(R10)(R11)R9, —C(R10)(R11)N(R10)R9, —C(R10)(R11)N(R10)(R11), —C(R10)(R11)SC(R10)(R11)(R9), R10S—, —C(Ra)(Rb)NRaC(Ra)(Rb)(R9), —C(Ra)(Rb)N(Ra)(Rb), —C(Ra)(Rb)C(Ra)(Rb)N(Ra)(Rb), —C(O)C(Ra)(Rb)N(Ra)(Rb), —C(Ra)(Rb)N(Ra)C(O)R9, —C(O)C(Ra)(Rb)S(Ra), C(Ra)(Rb)C(O)N(Ra)(Rb), —B(OH)2, —OCH2O— or 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl; wherein said groups are optionally substituted on either the carbon or the heteroatom with one to five substituents independently selected from C1-6 alkyl, halo, keto, cyano, haloalkyl, hydroxyalkyl, —OR9, —NO2, —NH2, —NHS(O)2R8, —R9SO2R12, —SO2R12, —SO(R12), —SR12, —SR9, —SOmN(Rc)(Rd), —SOmN(R10)C(O)(R12), —C(R10)(R11)N(R10)(R11), —C(R10)(R11)OH, —COOH, —C(Ra)(Rb)C(O)N(Ra)(Rb), —C(O)(Ra)(Rb), —N(R10)C(R10)(R11)(R9), —N(R10)CO(R9), —NH(CH2)2OH, —NHC(O)OR10, —Si(CH3)3, heterocycyl, aryl or heteroaryl; R8 is hydrogen or C1-6 alkyl; or R4 and R8 or can be taken together with any of the atoms to which they may be attached or are between them to form a 4-10 membered heterocyclyl ring system wherein said ring system, which may be monocyclic or bicyclic, is optionally substituted with one or two substituents independently selected from C1-6 alkyl, halo, hydroxyalkyl, hydroxy, keto, —OR10, —SR10 or —N(R10)2; R9 is selected from the group consisting of hydrogen, aryl, aryl(C1-4)alkyl, heteroaryl, heteroaryl(C1-4)alkyl, C3-8cycloalkyl, C3-8cycloalkyl(C1-4)alkyl, and heterocyclyl(C1-4)alkyl wherein said groups can be optionally substituted with one, two, or three substituents independently selected from halo, alkoxy or —SO2R12; R10 is hydrogen or C1-6 alkyl R11 is hydrogen or C1-6 alkyl; R12 is hydrogen or C1-6 alkyl which is optionally substituted with one, two, or three substituents independently selected from halo, alkoxy, cyano, —NR10 or —SR10; Ra is hydrogen, C1-6 alkyl, (C1-6 alkyl)aryl, (C1-6 alkyl)hydroxyl, —O(C1-6 alkyl), hydroxyl, halo, aryl, heteroaryl, C3-8 cycloalkyl, heterocyclyl, wherein said alkyl, aryl, heteroaryl, C3-8 cycloalkyl and heterocyclyl can be optionally substituted on either the carbon or the heteroatom with one, two, or three substituents independently selected from C1-6 alkyl or halo; Rb is hydrogen, C1-6 alkyl, (C1-6 alkyl)aryl, (C1-6 alkyl)hydroxyl, alkoxyl, hydroxyl, halo, aryl, heteroaryl, C3-8 cycloalkyl, heterocyclyl, wherein said alkyl, aryl, heteroaryl, C3-8 cycloalkyl and heterocyclyl can be optionally substituted on either the carbon or the heteroatom with one, two, or three substituents independently selected from C1-6 alkyl or halo; or Ra and Rb can be taken together with the carbon atom to which they are attached or are between them to form a C3-8 cycloalkyl ring or C3-8 heterocyclyl ring wherein said 3-8 membered ring system may be optionally substituted with one or two substituents independently selected from C1-6 alkyl and halo; Rc is hydrogen or C1-6 alkyl which is optionally substituted with one, two, or three substituents independently selected from halo or —OR9; Rd is hydrogen or C1-6 alkyl which is optionally substituted with one, two, or three substituents independently selected from halo or —OR9; or Rc and Rd can be taken together with the nitrogen atom to which they are attached or are between them to form a C3-8 heterocyclyl ring which is optionally substituted with one or two substituents independently selected from C1-6 alkyl, halo hydroxyalkyl, hydroxy, alkoxy or keto; n is independently selected from an integer from one to three; each m is independently selected from an integer from zero to two; and the pharmaceutically acceptable salts, stereoisomers and N-oxide derivatives thereof.
地址 Kirkland CA