Novel ptefb inhibiting macrocyclic compounds

Abstract

The present invention relates to novel modified macrocyclic compounds with improved tolerability of general formula (I) as described and defined herein, and methods for their preparation, their use for the treatment and/or prophylaxis of disorders, in particular of hyper-proliferative disorders and/or virally induced infectious diseases and/or of cardiovascular diseases. The invention further relates to intermediate compounds useful in the preparation of said compounds of general formula (I).

1 .- 27 . (canceled) 
     
     
         28 . A compound of general formula (7): 
       
         
           
           
               
               
           
         
         wherein: 
         Z is hydrogen or fluorine; 
         L is a C 3 -C 8 -alkylene moiety;
 wherein said moiety is optionally substituted with 
 (i) one substituent selected from hydroxy, —NR 8 R 9 , C 2 -C 3 -alkenyl-, C 2 -C 3 -alkynyl-, C 3 -C 4 -cycloalkyl-, hydroxy-C 1 -C 3 -alkyl, and —(CH 2 )NR 8 R 9 , and/or 
 (ii) one or two or three or four substituents, identically or differently, selected from halogen and C 1 -C 3 -alkyl-; 
 or wherein 
 one carbon atom of said C 3 -C 8 -alkylene moiety forms a three- or four-membered ring together with a bivalent moiety to which it is attached, wherein said bivalent moiety is selected from —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, and —CH 2 OCH 2 —; 
 
         R 1  is C 1 -C 6 -alkyl-, C 3 -C 6 -alkenyl-, C 3 -C 7 -cycloalkyl-, or heterocyclyl-;
 wherein said group is optionally substituted with one or two or three substituents, identically or differently, selected from the group consisting of hydroxy, cyano, halogen, C 1 -C 6 -alkyl-, halo-C 1 -C 3 -alkyl-, C 1 -C 6 -alkoxy-, C 1 -C 3 -fluoroalkoxy-, —NH 2 , alkylamino-, dialkylamino-, acetylamino-, N-methyl-N-acetylamino-, cyclic amines, —OP(═O)(OH) 2 , —C(═O)OH, and —C(═O)NH 2 ; 
 
         R 2  is hydrogen, fluorine, chlorine, bromine, cyano, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, halo-C 1 -C 3 -alkyl-, or C 1 -C 3 -fluoroalkoxy-; 
         R 3  and R 4  are independently from each other, a group selected from hydrogen, fluorine, chlorine, bromine, cyano, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, halo-C 1 -C 3 -alkyl-, and C 1 -C 3 -fluoroalkoxy-; and 
         R 8  and R 9  are independently from each other, a group selected from hydrogen, C 1 -C 6 -alkyl-, C 3 -C 7 -cycloalkyl-, heterocyclyl-, phenyl-, benzyl-, and heteroaryl-;
 wherein said C 1 -C 6 -alkyl-, C 3 -C 7 -cycloalkyl-, heterocyclyl-, phenyl-, benzyl- or heteroaryl-group is optionally substituted with one, two or three substituents, identically or differently, selected from the group consisting of halogen, hydroxy, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, —NH 2 , alkylamino-, dialkylamino-, acetylamino-, N-methyl-N-acetylamino-, cyclic amines, halo-C 1 -C 3 -alkyl-, and C 1 -C 3 -fluoroalkoxy-, or 
 
         R 8  and R 9 , together with the nitrogen atom they are attached to, form a cyclic amine; 
         or salt thereof. 
       
     
     
         29 . The compound of  claim 28 , wherein:
 Z is hydrogen or fluorine;   L is a C 3 -C 5 -alkylene moiety,   wherein said moiety is optionally substituted with
 i) one substituent selected from hydroxy, C 3 -C 4 -cycloalkyl-, and hydroxy-C 1 -C 3 -alkyl-, and —(CH 2 )NR 8 R 9 , and/or 
 ii) one or two or three substituents, identically or differently, selected from halogen and C 1 -C 3 -alkyl-; 
   R 1  is C 1 -C 6 -alkyl- or C 3 -C 5 -cycloalkyl-;
 wherein said group is optionally substituted with one or two or three substituents, identically or differently, selected from the group consisting of hydroxy, cyano, halogen, C 1 -C 3 -alkyl-, fluoro-C 1 -C 2 -alkyl-, C 1 -C 3 -alkoxy-, C 1 -C 2 -fluoroalkoxy-, —NH 2 , alkylamino-, dialkylamino-, cyclic amines, —OP(═O)(OH) 2 , —C(═O)OH, and —C(═O)NH 2 ; 
   R 2  is hydrogen, fluorine, chlorine, cyano, C 1 -C 2 -alkyl-, C 1 -C 2 -alkoxy-, fluoro-C 1 -C 2 -alkyl-, or C 1 -C 2 -fluoroalkoxy-;   R 3  and R 4  are independently from each other, a group selected from hydrogen, fluorine, chlorine, cyano, C 1 -C 2 -alkyl-, C 1 -C 2 -alkoxy-, fluoro-C 1 -C 2 -alkyl-, and C 1 -C 2 -fluoroalkoxy-; and   R 8  and R 9  are independently from each other, a group selected from hydrogen, C 1 -C 6 -alkyl-, C 3 -C 5 -cycloalkyl-, phenyl-, and benzyl-;
 wherein said C 1 -C 6 -alkyl-, C 3 -C 5 -cycloalkyl-, phenyl- or benzyl- group is optionally substituted with one, two or three substituents, identically or differently, selected from the group consisting of halogen, hydroxy, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, —NH 2 , alkylamino-, dialkylamino-, cyclic amines, fluoro-C 1 -C 2 -alkyl-, and C 1 -C 2 -fluoroalkoxy-, or 
   R 8  and R 9 , together with the nitrogen atom they are attached to, form a cyclic amine;   or a salt thereof.   
     
     
         30 . The compound of  claim 28 , wherein;
 Z is hydrogen or fluorine;   L is a C 3 -C 5 -alkylene moiety,
 wherein said moiety is optionally substituted with 
 (i) one substituent selected from C 3 -C 4 -cycloalkyl- and hydroxymethyl, and/or 
 (ii) one or two or three C 1 -C 2 -alkyl- group substituents, identically or differently; 
   R 1  is C 1 -C 4 -alkyl- or C 3 -C 5 -cycloalkyl-;
 wherein said group is optionally substituted with one or two or three substituents, identically or differently, selected from the group consisting of hydroxy, cyano, halogen, C 1 -C 2 -alkyl-, C 1 -C 2 -alkoxy-, —NH 2 , and —C(═O)OH; 
   R 2  is hydrogen, fluorine, chlorine, cyano, methyl-, methoxy-, trifluoromethyl-, or trifluoromethoxy-;   R 3  is hydrogen, fluorine, chlorine, cyano, methyl-, methoxy-, trifluoromethyl-, or trifluoromethoxy-;   R 4  is hydrogen or fluorine;   or a salt thereof.   
     
     
         31 . The compound of  claim 28 , wherein;
 Z is hydrogen or fluorine;   L is C 3 -C 5 -alkylene;   R 1  is C 1 -C 4 -alkyl optionally substituted with one or two substituents, identically or differently, selected from the group consisting of hydroxy, C 1 -C 2 -alkoxy-, —NH 2 , and —C(═O)OH;   R 2  is hydrogen or fluorine;   R 3  is hydrogen, fluorine, or methoxy; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         32 . The compound of  claim 28 , wherein;
 L is C 3 -C 5 -alkylene;   or a salt thereof.   
     
     
         33 . The compound of  claim 28 , wherein;
 Z is hydrogen or fluorine;   L is C 3 -C 5 -alkylene;   R 1  is methyl;   R 2  is hydrogen;   R 3  is hydrogen or fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         34 . The compound of  claim 28 , wherein:
 Z is hydrogen or fluorine;   L is C 3 -C 5 -alkylene;   R 1  is C 1 -C 3 -alkyl;   R 2  is hydrogen or fluorine;   R 3  is hydrogen, fluorine, or methoxy; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         35 . The compound of  claim 28 , wherein:
 Z is hydrogen or fluorine;   L is C 4 -C 5 -alkylene;   R 1  is methyl;   R 2  is hydrogen;   R 3  is hydrogen or fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         36 . The compound of  claim 28 , wherein;
 Z is hydrogen or fluorine,   R 3  is fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         37 . The compound of  claim 28 , wherein:
 Z is hydrogen or fluorine,   L is C 3 -C 5 -alkylene;   R 1  is methyl;   R 2  is hydrogen;   R 3  is fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         38 . A compound of general formula (19): 
       
         
           
           
               
               
           
         
         wherein: 
         Z is hydrogen or fluorine; 
         L is a C 3 -C 8 -alkylene moiety;
 wherein said moiety is optionally substituted with 
 (i) one substituent selected from hydroxy, —NR 8 R 9 , C 2 -C 3 -alkenyl-, C 2 -C 3 -alkynyl-, 
 C 3 -C 4 -cycloalkyl-, hydroxy-C 1 -C 3 -alkyl, and —(CH 2 )NR 8 R 9 , and/or (ii) one or two or three or four substituents, identically or differently, selected from halogen and C 1 -C 3 -alkyl-; 
 or wherein 
 one carbon atom of said C 3 -C 8 -alkylene moiety forms a three- or four-membered ring together with a bivalent moiety to which it is attached, wherein said bivalent moiety is selected from —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, and —CH 2 OCH 2 —; 
 
         R 1  is C 1 -C 6 -alkyl-, C 3 -C 6 -alkenyl-, C 3 -C 7 -cycloalkyl-, or heterocyclyl-;
 wherein said group is optionally substituted with one or two or three substituents, identically or differently, selected from the group consisting of hydroxy, cyano, halogen, C 1 -C 6 -alkyl-, halo-C 1 -C 3 -alkyl-, C 1 -C 6 -alkoxy-, C 1 -C 3 -fluoroalkoxy-, —NH 2 , alkylamino-, dialkylamino-, acetylamino-, N-methyl-N-acetylamino-, cyclic amines, —OP(═O)(OH) 2 , —C(═O)OH, and —C(═O)NH 2 ; 
 
         R 2  is hydrogen, fluorine, chlorine, bromine, cyano, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, halo-C 1 -C 3 -alkyl-, or C 1 -C 3 -fluoroalkoxy-; 
         R 3  and R 4  are independently from each other, a group selected from hydrogen, fluorine, chlorine, bromine, cyano, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, halo-C 1 -C 3 -alkyl-, and C 1 -C 3 -fluoroalkoxy-; and 
         R 8  and R 9  are independently from each other, a group selected from hydrogen, C 1 -C 6 -alkyl-, C 3 -C 7 -cycloalkyl-, heterocyclyl-, phenyl-, benzyl-, and heteroaryl-;
 wherein said C 1 -C 6 -alkyl-, C 3 -C 7 -cycloalkyl-, heterocyclyl-, phenyl-, benzyl- or heteroaryl-group is optionally substituted with one, two or three substituents, identically or differently, selected from the group consisting of halogen, hydroxy, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, —NH 2 , alkylamino-, dialkylamino-, acetylamino-, N-methyl-N-acetylamino-, cyclic amines, halo-C 1 -C 3 -alkyl-, and C 1 -C 3 -fluoroalkoxy-, or 
 
         R 8  and R 9 , together with the nitrogen atom they are attached to, form a cyclic amine; 
         or salt thereof. 
       
     
     
         39 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine;   L is a C 3 -C 5 -alkylene moiety,   wherein said moiety is optionally substituted with
 i) one substituent selected from hydroxy, C 3 -C 4 -cycloalkyl-, and hydroxy-C 1 -C 3 -alkyl-, and —(CH 2 )NR 8 R 9 , and/or 
 ii) one or two or three substituents, identically or differently, selected from halogen and C 1 -C 3 -alkyl-; 
   R 1  is C 1 -C 6 -alkyl- or C 3 -C 5 -cycloalkyl-;
 wherein said group is optionally substituted with one or two or three substituents, identically or differently, selected from the group consisting of hydroxy, cyano, halogen, C 1 -C 3 -alkyl-, fluoro-C 1 -C 2 -alkyl-, C 1 -C 3 -alkoxy-, C 1 -C 2 -fluoroalkoxy-, —NH 2 , alkylamino-, dialkylamino-, cyclic amines, —OP(═O)(OH) 2 , —C(═O)OH, and —C(═O)NH 2 ; 
   R 2  is hydrogen, fluorine, chlorine, cyano, C 1 -C 2 -alkyl-, C 1 -C 2 -alkoxy-, fluoro-C 1 -C 2 -alkyl-, or C 1 -C 2 -fluoroalkoxy-;   R 3  and R 4  are independently from each other, a group selected from hydrogen, fluorine, chlorine, cyano, C 1 -C 2 -alkyl-, C 1 -C 2 -alkoxy-, fluoro-C 1 -C 2 -alkyl-, and C 1 -C 2 -fluoroalkoxy-; and   R 8  and R 9  are independently from each other, a group selected from hydrogen, C 1 -C 6 -alkyl-, C 3 -C 5 -cycloalkyl-, phenyl-, and benzyl-;
 wherein said C 1 -C 6 -alkyl-, C 3 -C 5 -cycloalkyl-, phenyl- or benzyl- group is optionally substituted with one, two or three substituents, identically or differently, selected from the group consisting of halogen, hydroxy, C 1 -C 3 -alkyl-, C 1 -C 3 -alkoxy-, —NH 2 , alkylamino-, dialkylamino-, cyclic amines, fluoro-C 1 -C 2 -alkyl-, and C 1 -C 2 -fluoroalkoxy-, or 
   R 8  and R 9 , together with the nitrogen atom they are attached to, form a cyclic amine;   or a salt thereof.   
     
     
         40 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine;   L is a C 3 -C 5 -alkylene moiety,
 wherein said moiety is optionally substituted with 
 (i) one substituent selected from C 3 -C 4 -cycloalkyl- and hydroxymethyl, and/or 
 (ii) one or two or three C 1 -C 2 -alkyl- group substituents, identically or differently; 
   R 1  is C 1 -C 4 -alkyl- or C 3 -C 5 -cycloalkyl-;
 wherein said group is optionally substituted with one or two or three substituents, identically or differently, selected from the group consisting of hydroxy, cyano, halogen, C 1 -C 2 -alkyl-, C 1 -C 2 -alkoxy-, —NH 2 , and —C(═O)OH; 
   R 2  is hydrogen, fluorine, chlorine, cyano, methyl-, methoxy-, trifluoromethyl-, or trifluoromethoxy-;   R 3  is hydrogen, fluorine, chlorine, cyano, methyl-, methoxy-, trifluoromethyl-, or trifluoromethoxy-;   R 4  is hydrogen or fluorine;   or a salt thereof.   
     
     
         41 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine;   L is C 3 -C 5 -alkylene;   R 1  is C 1 -C 4 -alkyl optionally substituted with one or two substituents, identically or differently, selected from the group consisting of hydroxy, C 1 -C 2 -alkoxy-, —NH 2 , and —C(═O)OH;   R 2  is hydrogen or fluorine;   R 3  is hydrogen, fluorine, or methoxy; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         42 . The compound of  claim 38 , wherein:
 L is C 3 -C 5 -alkylene;   or a salt thereof.   
     
     
         43 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine;   L is C 3 -C 5 -alkylene;   R 1  is methyl;   R 2  is hydrogen;   R 3  is hydrogen or fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         44 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine;   L is C 3 -C 5 -alkylene;   R 1  is C 1 -C 3 -alkyl;   R 2  is hydrogen or fluorine;   R 3  is hydrogen, fluorine, or methoxy; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         45 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine;   L is C 4 -C 5 -alkylene;   R 1  is methyl;   R 2  is hydrogen;   R 3  is hydrogen or fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         46 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine,   R 3  is fluorine; and   R 4  is hydrogen;   or a salt thereof.   
     
     
         47 . The compound of  claim 38 , wherein:
 Z is hydrogen or fluorine,   L is C 3 -C 5 -alkylene;   R 1  is methyl;   R 2  is hydrogen;   R 3  is fluorine; and   R 4  is hydrogen;   or a salt thereof.