US2023310373A1PendingUtilityA1

Methods for treating pulmonary emphysema using substituted 2-aza-bicyclo[2.2.1]heptane-3-carboxylic acid (benzyl-cyano-methyl)-amides inhibitors of cathepsin c

Assignee: BOEHRINGER INGELHEIM INTPriority: Mar 14, 2013Filed: Jun 8, 2023Published: Oct 5, 2023
Est. expiryMar 14, 2033(~6.7 yrs left)· nominal 20-yr term from priority
A61K 31/403C07D 209/52A61K 31/4035A61K 31/4045A61K 31/4155A61K 31/4192A61K 31/438A61K 31/496A61K 31/5383A61K 31/551A61K 45/06C07D 401/12C07D 403/12C07D 403/14C07D 405/12C07D 487/10C07D 498/04C07D 471/08A61K 31/397A61K 31/404A61K 31/416A61K 31/473C07D 401/10C07D 409/12C07D 413/14C07D 417/12A61K 31/423Y02A50/30A61P 1/04A61P 11/00A61P 11/06A61P 15/00A61P 17/00A61P 17/06A61P 19/02A61P 25/04A61P 27/00A61P 29/00A61P 31/00A61P 31/04A61P 31/12A61P 31/18A61P 35/00A61P 37/00A61P 37/06A61P 37/08A61P 43/00A61P 7/00A61P 9/10
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Claims

Abstract

This invention relates to 2-Aza-bicyclo[2.2.1]heptane-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.

Claims

exact text as granted — not AI-modified
1 : A compound of formula 1 
       
         
           
           
               
               
           
         
         wherein 
         R 1  is independently selected from H, C 1-6 -alkyl-, halogen, HO—, C 1-6 -alkyl-O—, H 2 N—, C 1-6 -alkyl-HN—, (C 1-6 -alkyl) 2 N— and C 1-6 -alkyl-C(O)HN—; 
         or two R 1  are together C 1-4 -alkylene; 
         R 2  is selected from
 R 2.1 ; 
 aryl-; optionally substituted with one, two or three residues independently selected from R 2.1 ; optionally substituted with one R 2.3 ; 
 C 5-10 -heteroaryl-; containing one, two, three or four heteroatoms independently selected from 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 R 2.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.2 ; wherein a carbon atom of the ring is optionally substituted with one R 2.3 ; a nitrogen atom of the ring is optionally substituted with one R 2.4 ; and 
 C 5-10 -heterocyclyl-; containing one, two, three or four heteroatoms independently selected from 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 R 2.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.2 ; wherein a carbon atom of the ring is optionally substituted with one R 2.3  or one R 2.5 ; a nitrogen atom of the ring is optionally substituted with one R 2.4  or 
 R 2  and R 4  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 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 R 2.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.2 ; 
 
         R 2.1  is independently selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-6 -alkylene-, R 2.1.1 -A-, C 1-6 -alkyl-A-, C 3-8 -cycloalkyl-A-, C 1-6 -haloalkyl-A-, R 2.1.1 —C 1-6 -alkylene-A-, C 1-6 -alkyl-A-C 1-6 -alkylene-, C 3-8 -cycloalkyl-A-C 1-6 -alkylene-, C 1-6 -haloalkyl-A-C 1-6 -alkylene-, R 2.1.1 —C 1-6 -alkylene-A-C 1-6 -alkylene-, R 2.1.1 -A-C 1-6 -alkylene-, HO—C 1-6 -alkylene-A-, HO—C 1-6 -alkylene-A-C 1-6 -alkylene-, C 1-6 -alkyl-O—C 1-6 -alkylene-A- and C 1-6 -alkyl-O—C 1-6 -alkylene-A-C 1-6 -alkylene-
 R 2.1.1  is independently selected from
 aryl-; optionally substituted independently from each other with one, two or three R 2.1.1.1 ; 
 C 5-10 -heteroaryl-; containing one, two, three or four heteroatoms independently selected from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-; containing one, two, three or four heteroatoms independently selected from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-6 -alkyl-, C 1-6 -alkyl-O—, C 1-6 -haloalkyl-, C 1-6 -haloalkyl-O— and C 3-8 -cycloalkyl-; 
 R 2.1.1.2  is independently selected from O═, C 1-6 -alkyl-, C 1-6 -haloalkyl-;
 C 3-8 -cycloalkyl-, C 1-6 -alkyl-O—C 1-6 -alkyl-, H(O)C—, C 1-6 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl-; 
 
 
         R 2.2  is independently selected from H-A-C 1-6 -alkylene-, C 3-8 -cycloalkyl-, C 1-6 -alkyl-A-C 1-6 -alkylene-, C 3-8 -cycloalkyl-A-C 1-6 -alkylene-, C 1-6 -haloalkyl-A-C 1-6 -alkylene-, R 2.1.1 -A-C 1-6 -alkylene-, C 1-6 -alkyl-S(O) 2 — and C 1-6 -alkyl-C(O)—, R 2.1.1 -A-; 
         R 2.3  and R 4  are together selected 
         from —O—, —S—, —N(R 2.3.1 )—, —C(O)N(R 2.3.1 )—, —N(R 2.3.1 )C(O)—, —S(O) 2 N(R 2.3.1 )—, —N(R 2.3.1 )S(O) 2 —, —C(O)O—, —OC(O)—, —C(O)—, —S(O)—, —S(O) 2 —, R 2.3 , 
         R 2.3 , —C(R 2.3.2 )═C(R 2.3.2 )—, —C═N—, —N═C—, —C(R 2.3.2 ) 2 —O—, —O—C(R 2.3.2 ) 2 —, —C(R 2.3.2 ) 2 N(R 2.3.1 )—, and —N(R 2.3.1 )C(R 2.3.2 ) 2 — and —C 1-4 -alkylene-;
 R 2.3.1  is independently selected from H, C 1-6 -alkyl-, C 1-6 -haloalkyl-;
 C 3-8 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and 
 (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 
 R 2.3.2  is independently selected from H, C 1-6 -alkyl-, C 1-6 -haloalkyl-;
 C 3-8 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and 
 (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 
 
         R 2.4  and R 4  are together selected 
         from —N(R 2.4.1 )—, —C(O)N(R 2.4.1 )—, —N(R 2.4.1 )C(O)—, —S(O) 2 N(R 2.4.1 )—, —N(R 2.4.1 )S(O) 2 —, —C(O)—, —S(O)—, —S(O) 2 —, —C(R 2.4.2 )═C(R 2.4.2 )—, —C═N—, —N═C—, —C(R 2.4.2 ) 2 N(R 2.4.1 )— and —N(R 2.4.1 )C(R 2.4.2 ) 2 —, —C 1-4 -alkylene-; and
 R 2.4.1  is independently selected from H, C 1-6 -alkyl-, C 1-6 -haloalkyl-;
 C 3-8 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and 
 (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 
 R 2.4.2  is independently selected from H, C 1-6 -alkyl-, C 1-6 -haloalkyl-;
 C 3-8 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and 
 (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 
 
         R 2.5  and R 4  are together selected from —C(R 2.5.1 )═, ═C(R 2.5.1 )—, —N═; and
 R 2.5.1  is independently selected from H, C 1-6 -alkyl-, C 1-6 -haloalkyl-;
 C 3-8 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and 
 (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 
 
         R 3  is H or F; 
         R 4  is independently selected from F, Cl, phenyl-H 2 C—O—, HO—, C 1-6 -alkyl-, C 1-6 -haloalkyl-, C 3-8 -cycloalkyl-, C 1-6 -alkyl-O—, C 1-6 -haloalkyl-O—, C 1-6 -alkyl-HN—, (C 1-6 -alkyl) 2 -HN—, C 1-6 -alkyl-HN—C 1-4 -alkylene- and (C 1-6 -alkyl) 2 -HN—C 1-4 -alkylene-; 
         A is a bond or independently selected
 from —O—, —S—, —N(R 5 )—, —C(O)N(R 5 )—, —N(R 5 )C(O)—, —S(O) 2 N(R 5 )—, —N(R 5 )S(O) 2 —, —S(O)(═NR 5 )—N(R 5 )—, —N(R 5 )(NR 5 ═)S(O)—, —S(═NR 5 ) 2 —N(R 5 )—, —N(R 5 )(NR 5 ═) 2 S—, —C(R 5 )═C(R 5 )—, —C≡C—, —C(O)O—, —OC(O)—, —C(O)—, —S(O)—, —S(O) 2 —, —S(═NR 5 )—, —S(O)(═NR 5 )—, —S(═NR 5 ) 2 —, —(R 5 )(O)S═N—, —(R 5 N═)(O)S—, and —N═(O)(R 5 )S—; 
 
         R 5  is independently selected from H, C 1-6 -alkyl- and NC—; 
         or a salt thereof. 
       
     
     
         2 : The compound of formula 1, according to  claim 1 , wherein R 1  is R 1.a  and R 1.a  is independently selected from H, C 1-4 -alkyl-, F and HO—. 
     
     
         3 : The compound of formula 1, according to  claim 1 , wherein R 4  is R 4.a  and R 4.a  is F, Cl, phenyl-H 2 C—O—, HO—, C 1-4 -alkyl-, C 1-4 -haloalkyl-, C 3-6 -cycloalkyl-, C 1-4 -alkyl-O— and C 1-4 -haloalkyl-O—. 
     
     
         4 : The compound of formula 1, according to  claim 1 , wherein R 4  is R 4.b  and R 4.b  is F. 
     
     
         5 : The compound of formula 1, according to  claim 1 , wherein A is A a  and A a  is a bond or independently selected
 from —O—, —C(O)N(R 5 )—, —N(R 5 )C(O)—, —S(O) 2 N(R 5 )—, —N(R 5 )S(O) 2 —, —C(O)O—, —OC(O)—, —C(O)—, —S(O) 2 —, —(R 5 )(O)S═N—, —(R 5 N═)(O)S—, —N═(O)(R 5 )S— and R 5  is R 5.a  and R 5.a  is independently selected from H, C 1-4 -alkyl- and NC—.   
     
     
         6 : The compound of formula 1, according to  claim 1 , wherein R 2  is R 2.1  and
 R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl-, C 1-4 -haloalkyl-O— and C 3-6 -cycloalkyl-; and 
 R 2.1.1.2  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl. 
   
     
     
         7 : The compound of formula 1, according to  claim 1 , wherein R 2  is R 2.d  and R 2.d  is phenyl; optionally substituted with one, two or three residues independently selected from R 2.1  and
 R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl-, C 1-4 -haloalkyl-O— and C 3-6 -cycloalkyl-; and 
 R 2.1.12  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl. 
   
     
     
         8 : The compound of formula 1, according to  claim 1 , wherein R 2  is R 2.g  and R 2.g  is selected from 
       
         
           
           
               
               
           
         
         wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1 ; wherein possibly available nitrogen atoms of the ring are optionally and independently from each other substituted with R 2.2 ; and 
         R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl-, C 1-4 -haloalkyl-O— and C 3-6 -cycloalkyl-; and 
 R 2.1.1.2  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl; and 
 
         R 2.2  is R 2.2.a  and R 2.2.a  is independently selected from H-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, C 1-4 -alkyl-S(O) 2 — and C 1-4 -alkyl-C(O)—, R 2.1.1 -A-. 
       
     
     
         9 : The compound of formula 1, according to  claim 1 , wherein R 2  is R 2.j  and R 2.j  is selected from 
       
         
           
           
               
               
           
         
         wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1 ; wherein possibly available nitrogen atoms of the ring are optionally and independently from each other substituted with R 2.2 ; and 
         R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl- and C 1-4 -haloalkyl-O—, C 3-6 -cycloalkyl-; and 
 R 2.1.1.2  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl; and 
 
         R 2.2  is R 2.2.a  and R 2.2.a  is independently selected from H-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, C 1-4 -alkyl-S(O) 2 —, C 1-4 -alkyl-C(O)— and R 2.1.1 -A-. 
       
     
     
         10 : The compound of formula 1, according to  claim 1 , wherein R 2  is R 2.m  and R 2.m  is together with R 4  and 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 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 R 2.1 , wherein possibly available nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.2 ; and
 R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl-, C 1-4 -haloalkyl-O— and C 3-6 -cycloalkyl-; and 
 R 2.1.1.2  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl; and 
   R 2.2  is R 2.2.a  and R 2.2.a  is independently selected from H-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, C 1-4 -alkyl-S(O) 2 —, C 1-4 -alkyl-C(O)— and R 2.1.1 -A-.   
     
     
         11 : The compound of formula 1, according to  claim 1 , wherein R 2  is R 2.n  and R 2.n  is selected from aryl-, pyrazole, thiophene, furane; wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two, three or four R 2.1 ; wherein possibly available nitrogen atoms of the ring are optionally and independently from each other substituted with R 2.2 ; wherein a carbon atom of the ring is optionally substituted with one R 2.3 ; a nitrogen atom of the ring is optionally substituted with one R 2.4 ; or R 2.n  is selected from 
       
         
           
           
               
               
           
         
         wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two, three or four R 2.1 ; wherein possibly available nitrogen atoms of the ring are optionally and independently from each other substituted with R 2.2 ; wherein a carbon atom of the ring is optionally substituted with one R 2.3  or one R 2.5 ; a nitrogen atom of the ring is optionally substituted with one R 2.4 ; and 
         R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl-, C 1-4 -haloalkyl-O— and C 3-6 -cycloalkyl-; and 
 
         R 2.1.1.2  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl; and 
         R 2.2  is R 2.2.a  and R 2.2.a  is independently selected from H-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, C 1-4 -alkyl-S(O) 2 —, C 1-4 -alkyl-C(O)— and R 2.1.1 -A-; and 
         R 2.3  is together with R 4  a group R 2.3.a  and R 2.3.a  is selected
 from —O—, —S—, —N(R 2.3.1 )—, —C(O)N(R 2.3.1 )—, —N(R 2.3.1 )C(O)—, —S(O) 2 N(R 2.3.1 )—, —N(R 2.3.1 )S(O) 2 —, —C(O)O—, —OC(O)—, —C(O)—, —S(O)—, —S(O) 2 —, —C(R 2.3.2 )═C(R 2.3.2 )—, —C═N—, —N═C—, —C(R 2.3.2 ) 2 —O—, —O—C(R 2.3.2 ) 2 —, —C(R 2.3.2 ) 2 N(R 2.3.1 )—, —N(R 2.3.1 )C(R 2.3.2 ) 2 — and —C 1-4 -alkylene-; and 
 R 2.3.1  is independently selected from H, C 1-4 -alkyl-, C 1-4 -haloalkyl-, C 3-6 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 R 2.3.2  is independently selected from H, C 1-4 -alkyl-, C 1-4 -haloalkyl-, C 3-6 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; and 
 
         R 2.4  is together with R 4  a group R 2.4.a  and R 2.4.a  is selected
 from —N(R 2.4.1 )—, —C(O)N(R 2.4.1 )—, —N(R 2.4.1 )C(O)—, —S(O) 2 N(R 2.4.1 )—, —N(R 2.4.1 )S(O) 2 —, —C(O)—, —S(O)—, —S(O) 2 —, —C(R 2.4.2 )═C(R 2.4.2 )—, —C═N—, —N═C—, —C(R 2.4.2 ) 2 N(R 2.4.1 ), 
 and —N(R 2.4.1 )C(R 2.4.2 ) 2 —, —C 1-4 -alkylene-; and 
 R 2.4.1  is independently selected from H, C 1-4 -alkyl-, C 1-4 -haloalkyl-, C 3-6 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; 
 R 2.4.2  is independently selected from H, C 1-4 -alkyl-, C 1-4 -haloalkyl-, C 3-6 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-; and 
 
         R 2.5  is together with R 4  a group R 2.5.a  and R 2.5.a  is selected from —C(R 2.5.1 )═, ═C(R 2.5.1 )— and —N═; and
 R 2.5.1  is independently selected from H, C 1-4 -alkyl-, C 1-4 -haloalkyl-, C 3-6 -cycloalkyl-, HO—C 1-4 -alkylene-, (C 1-4 -alkyl)-O—C 1-4 -alkylene-, H 2 N—C 1-4 -alkylene-, (C 1-4 -alkyl)HN—C 1-4 -alkylene- and (C 1-4 -alkyl) 2 N—C 1-4 -alkylene-. 
 
       
     
     
         12 : The compound of formula 1 according to  claim 1 , wherein
 R 1  is R 1.b  and R 1.b  is H;   R 2  is R 2.q  and R 2.q  is selected from among the substituents (a1) to (q1)   
       
         
           
           
               
               
           
         
         
           
           
               
               
           
         
         wherein carbon atoms of the ring are optionally and independently from each other substituted with one, two, three or four R 2.1 ; wherein possibly available nitrogen atoms of the ring are optionally and independently from each other are substituted with R 2.2 ; 
         or a salt thereof. 
       
     
     
         13 : The compound of formula 1 according to  claim 1 , wherein R 2  is R 2.s  and R 2.s  is Phenyl-R 2.3 ,
 wherein the phenyl ring is optionally substituted with one or two residues R 2.1 , wherein
 R 2.1  is R 2.1.a  and R 2.1.a  is selected from H, halogen, NC—, O═, HO—, H-A-, H-A-C 1-4 -alkylene-, R 2.1.1 -A-, C 1-4 -alkyl-A-, C 3-6 -cycloalkyl-A-, C 1-4 -haloalkyl-A-, R 2.1.1 —C 1-4 -alkylene-A-, C 1-4 -alkyl-A-C 1-4 -alkylene-, C 3-6 -cycloalkyl-A-C 1-4 -alkylene-, C 1-4 -haloalkyl-A-C 1-4 -alkylene-, R 2.1.1 —C 1-4 -alkylene-A-C 1-4 -alkylene-, R 2.1.1 -A-C 1-4 -alkylene-, HO—C 1-4 -alkylene-A-, HO—C 1-4 -alkylene-A-C 1-4 -alkylene-, C 1-4 -alkyl-O—C 1-4 -alkylene-A- and C 1-4 -alkyl-O—C 1-4 -alkylene-A-C 1-4 -alkylene-; and 
 R 2.1.1  is R 2.1.1.a  and R 2.1.1.a  is selected from
 aryl-, optionally substituted independently from each other with one, two or three residues independently selected from R 2.1.1.1 ; 
 C 5-10 -heteroaryl-, containing one, two, three or four heteroatoms selected independently from 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; 
 C 5-10 -heterocyclyl-, containing one, two, three or four heteroatoms selected independently from S, S(O), S(O) 2 , O and N, and 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 R 2.1.1.1 ; wherein nitrogen atoms of the ring are optionally and independently from each other substituted with one, two or three R 2.1.1.2 ; and 
 
 R 2.1.1.1  is independently selected from halogen, HO—, O═, C 1-4 -alkyl-, C 1-4 -alkyl-O—, C 1-4 -haloalkyl-, C 1-4 -haloalkyl-O— and C 3-6 -cycloalkyl-; and 
 R 2.1.1.2  is independently selected from O═, C 1-4 -alkyl-, C 1-4 -haloalkyl-; C 3-6 -cycloalkyl-, C 1-4 -alkyl-O—C 1-4 -alkyl-, H(O)C—, C 1-4 -alkyl-(O)C—, tetrahydrofuranylmethyl- and tetrahydropyranylmethyl. 
   and R 2.s  and R 4  together denote a group (r1),   
       
         
           
           
               
               
           
         
         
           wherein the N-atom is optionally substituted with —R 2.2 , wherein 
           R 2.2  is independently selected from H-A-C 1-6 -alkylene-, C 3-8 -cycloalkyl-, C 1-6 -alkyl-A-C 1-6 -alkylene-, C 3-8 -cycloalkyl-A-C 1-6 -alkylene-, C 1-6 -haloalkyl-A-C 1-6 -alkylene-, R 2.1.1 -A-C 1-6 -alkylene-, C 1-6 -alkyl-S(O) 2 —, C 1-6 -alkyl-C(O)— and R 2.1.1 -A-; 
         
         or a salt thereof. 
       
     
     
         14 : A compound of formula 1′ 
       
         
           
           
               
               
           
         
         wherein R 1 , R 2 , R 3  and R 4  have the meaning of  claim 1 . 
       
     
     
         15 - 16 . (canceled) 
     
     
         17 : A pharmaceutical composition comprising a compound of formula 1 according to  claim 1  or a pharmaceutically acceptable salt thereof. 
     
     
         18 . (canceled) 
     
     
         19 : The pharmaceutical composition according to  claim 17  further comprising a pharmaceutically active compound selected from the group consisting of betamimetics, anticholinergics, corticosteroids, PDE4-inhibitors, LTD4-antagonists, EGFR-inhibitors, CRTH2 inhibitors, 5-LO-inhibitors, Histamine receptor antagonists, CCR9 antagonists and SYK-inhibitors, NE-inhibitors, MMP9 inhibitors and MMP12 inhibitors, or combinations of two or three of such pharmaceutically active compounds.

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