发明名称 Method of using substituted 2-Aza-bicyclo[2.2.2]octane-3-carboxylic acid (benzyl-cyano-methyl)-amides inhibitors of cathepsin C
摘要 This invention relates to 2-Aza-bicyclo[2.2.2]octane-3-carboxylic acid (benzyl-cyano-methyl)-amides of formula 1; and their use as inhibitors of Cathepsin C, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment and/or prevention of diseases connected with dipeptidyl peptidase I activity, e.g. respiratory diseases.
申请公布号 US9073869(B2) 申请公布日期 2015.07.07
申请号 US201414483217 申请日期 2014.09.11
申请人 Boehringer Ingelheim International GmbH 发明人 Anderskewitz Ralf;Grauert Matthias;Grundl Marc;Oost Thorsten;Pautsch Alexander;Peters Stefan
分类号 A61K31/439;A61K31/4725;A61K45/06;C07D221/22;C07D401/12;C07D417/12;C07D453/06 主分类号 A61K31/439
代理机构 代理人 Morris Michael P.;Royaee Atabak R.
主权项 1. A method of treating asthma and allergic diseases, gastrointestinal inflammatory diseases, eosinophilic diseases, chronic obstructive pulmonary disease, infection by pathogenic microbes, rheumatoid arthritis or atherosclerosis comprising administering to a patient a therapeutically effective amount of a compound of formula 1 wherein R1 is independently selected from among H, C1-6-alkyl-, halogen, HO—, C1-6-alkyl-O—, H2N—, C1-6-alkyl-HN—, (C1-6-alkyl)2N— and C1-6-alkyl-C(O)HN—; or two R1 are together C1-4-alkylene; R2 is selected from among R2.1;aryl-; optionally substituted with one, two or three residues independently selected from R2.1; optionally substituted with one R2.3;C5-10-heteroaryl-; containing one, two, three or four heteroatoms independently selected from among S, S(O), S(O)2, O and N, wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three R2.1; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R2.2; wherein a carbon atom of the ring is optionally substituted with one R2.3; a nitrogen atom of the ring is optionally substituted with one R2.4; — andC5-10-heterocyclyl-; containing one, two, three or four heteroatoms independently selected from among S, S(O), S(O)2, O and N, wherein the ring is fully or partially saturated, wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three or four R2.1; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R2.2; wherein a carbon atom of the ring is optionally substituted with one R2.3 or one R2.5; a nitrogen atom of the ring is optionally substituted with one R2.4 orR2 and R4 are together with two adjacent carbon atoms of the phenyl ring a 5- or 6-membered aryl or heteroaryl, containing one, two or three heteroatoms independently selected from among S, S(O), S(O)2, O and N, wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three R2.1; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R2.2; R2.1 is independently selected from among H, halogen, NC—, O═, HO—, H-A-, H-A-C1-6-alkylene-, R2.1.1-A-, C1-6-alkyl-A-, C3-8-cycloalkyl-A-, C1-6-haloalkyl-A-, R2.1.1—C1-6-alkylene-A-, C1-6-alkyl-A-C1-6-alkylene-, C3-8-cycloalkyl-A-C1-6-alkylene-, C1-6-haloalkyl-A-C1-6-alkylene-, R2.1.1—C1-6-alkylene-A-C1-6-alkylene-, R2.1.1-A-C1-6-alkylene-, HO—C1-6-alkylene-A-, HO—C1-6-alkylene-A-C1-6-alkylene-, C1-6-alkyl-O—C1-6-alkylene-A- and C1-6-alkyl-O—C1-6-alkylene-A-C1-6-alkylene- R2.1.1 is independently selected from among aryl-; optionally substituted independently from each other with one, two or three R2.1.1.1;C5-10-heteroaryl-; containing one, two, three or four heteroatoms independently selected from among S, S(O), S(O)2, O and N, wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three R2.1.1.1; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R2.1.1.2; — andC5-10-heterocyclyl-; containing one, two, three or four heteroatoms independently selected from among S, S(O), S(O)2, O and N, wherein the ring is fully or partially saturated, wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three or four R2.1.1.1; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R2.1.1.2;R2.1.1.1 is independently selected from among halogen, HO—, O═, C1-6-alkyl-, C1-6-alkyl-O—, C1-6-haloalkyl-, C1-6-haloalkyl-O— and C3-8-cycloalkyl-;R2.1.1.2 is independently selected from among O═, C1-6-alkyl-, C1-6-haloalkyl-; C3-8-cycloalkyl-, C1-6-alkyl-O—C1-6-alkyl-, H(O)C—, C1-6-alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl-; R2.2 is independently selected from among H-A-C1-6-alkylene-, C3-8-cycloalkyl-, C1-6-alkyl-A-C1-6-alkylene-, C3-8-cycloalkyl-A-C1-6-alkylene-, C1-6-haloalkyl-A-C1-6-alkylene-, R2.1.1-A-C1-6-alkylene-, C1-6-alkyl-S(O)2—, C1-6-alkyl-C(O)— and R2.1.1-A-; R2.3 and R4 are together selected from among —O—, —S—, —N(R2.3.1)—, —C(O)N(R2.3.1)—, —N(R2.3.1)C(O)—, —S(O)2N(R2.3.1)—, —N(R2.3.1)S(O)2—, —C(O)O—, —OC(O)—, —C(O)—, —S(O)—, —S(O)2—, R2.3, R2.3, —C(R2.3.2)═C(R2.3.2)—, —C═N—, —N═C—, —C(R2.3.2)2—O—, —O—C(R2.3.2)2—, —C(R2.3.2)2N(R2.3.1)—, —N(R2.3.1)C(R2.3.2)2— and —C1-4-alkylene-; R2.3.1 is independently selected from among H, C1-6-alkyl-, C1-6-haloalkyl-; C3-8-cycloalkyl-, HO—C1-4-alkylene-, (C1-4-alkyl)-O—C1-4-alkylene-, H2N—C1-4-alkylene-, (C1-4-alkyl)HN—C1-4-alkylene- and (C1-4-alkyl)2N—C1-4-alkylene-;R2.3.2 is independently selected from among H, C1-6-alkyl-, C1-6-haloalkyl-; C3-8-cycloalkyl-, HO—C1-4-alkylene-, (C1-4-alkyl)-O—C1-4-alkylene-, H2N—C1-4-alkylene-, (C1-4-alkyl)HN—C1-4-alkylene- and (C1-4-alkyl)2N—C1-4-alkylene-; R2.4 and R4 are together selected from among —N(R2.4.1)—, —C(O)N(R2.4.1)—, —N(R2.4.1)C(O)—, —S(O)2N(R2.4.1)—, —N(R2.4.1)S(O)2—, —C(O)—, —S(O)—, —S(O)2—, —C(R2.4.2)═C(R2.4.2)—, —C═N—, —N═C—, —C(R2.4.2)2N(R2.4.1)— and —N(R2.4.1)C(R2.4.2)2—, —C1-4-alkylene-; and R2.4.1 is independently selected from among H, C1-6-alkyl-, C1-6-haloalkyl-; C3-8-cycloalkyl-, HO—C1-4-alkylene-, (C1-4-alkyl)-O—C1-4-alkylene-, H2N—C1-4-alkylene-, (C1-4-alkyl)HN—C1-4-alkylene- and (C1-4-alkyl)2N—C1-4-alkylene-;R2.4.2 is independently selected from among H, C1-6-alkyl-, C1-6-haloalkyl-; C3-8-cycloalkyl-, HO—C1-4-alkylene-, (C1-4-alkyl)-O—C1-4-alkylene-, H2N—C1-4-alkylene-, (C1-4-alkyl)HN—C1-4-alkylene- and (C1-4-alkyl)2N—C1-4-alkylene-; R2.5 and R4 are together selected from among —C(R2.5.1)═, ═C(R2.5.1)— — and —N═; and R2.5.1 is independently selected from among H, C1-6-alkyl-, C1-6-haloalkyl-; C3-8-cycloalkyl-, HO—C1-4-alkylene-, (C1-4-alkyl)-O—C1-4-alkylene-, H2N—C1-4-alkylene-, (C1-4-alkyl)HN—C1-4-alkylene- and (C1-4-alkyl)2N—C1-4-alkylene-; R3 is H or F; R4 is independently selected from among H, F, Cl, phenyl-H2C—O—, HO—, C1-6-alkyl-, C1-6-haloalkyl-, C3-8-cycloalkyl-, C1-6-alkyl-O—, C1-6-haloalkyl-O—, C1-6-alkyl-HN—, (C1-6-alkyl)2-HN—, C1-6-alkyl-HN—C1-4-alkylene- and (C1-6-alkyl)2-HN—C1-4-alkylene-; A is a bond or independently selected from among —O—, —S—, —N(R5)—, —C(O)N(R5)—, —N(R5)C(O)—, —S(O)2N(R5)—, —N(R5)S(O)2—, —S(O)(═NR5)—N(R5)—, —N(R5)(NR5═)S(O)—, —S(═NR5)2—N(R5)—, —N(R5)(NR5═)2S—, —C(R5)═C(R5)—, —C≡C—, —C(O)O—, —OC(O)—, —C(O)—, —S(O)—, —S(O)2—, —S(═NR5)—, —S(O)(═NR5)—, —S(═NR5)2—, —(R5)(O)S ═N—, —(R5N═)(O)S— and —N═(O)(R5)S—; R5 is independently selected from among H, C1-6-alkyl- and NC—; or a pharmaceutically acceptable salt thereof.
地址 Ingelheim am Rhein DE