Imidazolo-5-yl-2-anilino-pyrimidines as agents for the inhibition of the cell proliferation

Abstract

Compounds of the formula (I): wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , p, q, and n are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.

1 - 17 . (canceled)  
     
     
         18 . A method for treating cancer in a warm-blooded animal in need thereof, said method comprising administering to said animal an effective amount of a compound of formula (I):  
       
         
           
           
               
               
           
         
       
       wherein: 
 R 1  is halo, nitro, cyano, hydroxy, amino, carboxy, carbamoyl, mercapto, C 1-6 alkyl, C 1-6 alkoxy, C 2-6 alkenyl or C 2-6 alkynyl;  
 p is 0-4; wherein the values of R 1  may be the same or different;  
 R 2  is sulphamoyl or a group R a —R b —;  
 q is 0-2; wherein the values of R 2  maybe the same or different; and wherein p+q=0-5;  
 R 3  is halo, nitro, cyano, hydroxy, trifluoromethyl, trifluoromethoxy, amino, carboxy, carbamoyl, mercapto, sulphamoyl, C 1-3 alkyl, C 2-3 alkenyl, C 2-3 alkynyl, C 1-3 alkoxy, C 1-3 alkanoyl, N-(C 1-3 alkyl)amino, N,N-(C 1-3 alkyl) 2 amino, C 1-3 alkanoylamino, N-(C 1-3 alkyl)carbamoyl, N,N-(C 1-3 alkyl) 2 carbamoyl, C 1-3 alkylS(O) a  wherein a is 0 to 2, N-(C 1-3 alkyl)sulphamoyl or N,N-(C 1-3 alkyl) 2 sulphamoyl; wherein R 3  may be optionally substituted on carbon by one or more R c ;  
 n is 0 to 2, wherein the values of R 3  may be the same or different;  
 R 4  is hydrogen, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, phenyl or a carbon-linked heterocyclic group; wherein R 4  may be optionally substituted on carbon by one or more R d ; and wherein if said heterocyclic group contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R n ;  
 R 5  and R 6  are independently selected from hydrogen, halo, nitro, cyano, hydroxy, trifluoromethoxy, amino, carboxy, carbamoyl, mercapto, sulphamoyl, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 1-6 alkanoyl, C 1-6 alkanoyloxy, N-(C 1-6 alkyl)amino, N,N-(C 1-6 alkyl) 2 amino, C 1-6 alkanoylamino, N-(C 1-6 alkyl)carbamoyl, N,N-(C 1-6 alkyl) 2 carbamoyl, C 1-6 alkylS(O) a  wherein a is 0 to 2, C 1-6 alkoxycarbonyl, N-(C 1-6 alkyl)sulphamoyl, N,N-(C 1-6 alkyl) 2 sulphamoyl, C 1-6 alkylsulphonylamino, C 3-8 cycloalkyl or a 4-7 membered saturated heterocyclic group; wherein R 5  and R 6  independently of each other may be optionally substituted on carbon by one or more R e ; and wherein if said 4-7 membered saturated heterocyclic group contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R f ;  
 R a  is selected from C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, C 3-8 cycloalkylC 1-6 alkyl, phenyl, a heterocyclic group, phenylC 1-6 alkyl or (heterocyclic group)C 1-6 alkyl; wherein R a  may be optionally substituted on carbon by one or more R g ; and wherein if said heterocyclic group contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R h ;  
 R b  is —C(O)—, —N(R m )C(O)—, —C(O)N(R m )—, —S(O) r —, —OC(O)N(R m )SO 2 —, —SO 2 N(R m )— or —N(R m )SO 2 —; wherein R m  is hydrogen or C 1-6 alkyl optionally substituted by one or more and R i  and r is 1-2;  
 R d , R g  and R i  are independently selected from halo, nitro, cyano, hydroxy, amino, carboxy, carbamoyl, mercapto, sulphamoyl, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 1-6 alkoxy, C 1-6 alkoxyC 1-6 alkoxy, C 1-6 alkoxyC 1-6 alkoxyC 1-6 alkoxy, C 1-6 alkanoyl, C 1-6 alkanoyloxy, N-(C 1-6 alkyl)amino, N,N-(C 1-6 alkyl) 2 amino, C 1-6 alkanoylamino, N-(C 1-6 alkyl)carbamoyl, N,N-(C 1-6 alkyl) 2 carbamoyl, C 1-6 alkylS(O) a  wherein a is 0 to 2, C 1-6 alkoxycarbonyl, N-(C 1-6 alkyl)sulphamoyl, N,N-(C 1-6 alkyl) 2 sulphamoyl, C 1-6 alkylsulphonylamino, C 3-8 cycloalkyl, phenyl, heterocyclic group, phenylC 1-6 alkyl-R o —, (heterocyclic group)C 1-6 alkyl-R o —, phenyl-R o —or (heterocyclic group)-R o —; wherein R d , R g  and R i  independently of each other may be optionally substituted on carbon by one or more R j ; and wherein if said heterocyclic group contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R k ;  
 R o  is —O—, —N(R p )—, —C(O)—, —N(R p )C(O)—, —C(O)N(R p )—, —S(O) s —, —SO 2 N(R p )— or —N(R p )SO 2 —; wherein R p  is hydrogen or C 1-6 alkyl and s is 0-2;  
 R f , R h , R k  and R n  are independently selected from C 1-4 alkyl, C 1-4 alkanoyl, C 1-4 alkylsulphonyl, C 1-4 alkoxycarbonyl, carbamoyl, N-(C 1-4 alkyl)carbamoyl, N,N-(C 1-4 alkyl)carbamoyl, benzyl, benzyloxycarbonyl, benzoyl and phenylsulphonyl; wherein R f , R h , R k  and R n  independently of each other may be optionally substituted on carbon by on or more R 1 ; and  
 R c , R e , R l  and R j  are independently selected from halo, nitro, cyano, hydroxy, trifluoromethoxy, trifluoromethyl, amino, carboxy, carbamoyl, mercapto, sulphamoyl, methyl, ethyl, methoxy, ethoxy, acetyl, acetoxy, methylamino, ethylamino, dimethylamino, diethylamino, N-methyl-N-ethylamino, acetylamino, N-methylcarbamoyl, N-ethylcarbamoyl, N,N-dimethylcarbamoyl, N,N-diethylcarbamoyl, N-methyl-N-ethylcarbamoyl, methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, mesyl, ethylsulphonyl, methoxycarbonyl, ethoxycarbonyl, N-methylsulphamoyl, N-ethylsulphamoyl, N,N-dimethylsulphamoyl, N,N-diethylsulphamoyl or N-methyl-N-ethylsulphamoyl;  
 or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof.  
 
     
     
         19 . The method according to  claim 18  wherein R 1  is halo, amino, C 1-6 alkyl or C 1-6 alkoxy.  
     
     
         20 . The method according to  claim 18  wherein p is 0-2 and wherein the values of R 1  may be the same or different.  
     
     
         21 . The method according to  claim 18  wherein R 2  is sulphamoyl or a group R a —R b —; wherein 
 R a  is selected from C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-8 cycloalkyl, phenyl or a heterocyclic group; wherein R a  may be optionally substituted on carbon by one or more R g ;    R b  is —N(R m )C(O)—, —C(O)N(R m )—, —S(O) r —, —OC(O)N(R m )SO 2 —, —SO 2 N(R m )— or —N(R m )SO 2 —; wherein R m  is hydrogen or C 1-6 alkyl and r is 2;    R g  is selected from halo, hydroxy, amino, cyano, carbamoyl, C 1-6 alkyl, C 1-6 alkoxy, C 1-6 alkoxyC 1-6 alkoxy, C 1-6 alkoxyC 1-6 alkoxyC 1-6 alkoxy, N,N-(C 1-6 alkyl) 2 amino, C 1-6 alkylS(O) a  wherein a is 2, C 3-8 cycloalkyl, phenyl, heterocyclic group, phenylC 1-6 alkyl-R o — or (heterocyclic group)-R o —; wherein R g  may be optionally substituted on carbon by one or more R j ;    R o  is —O—; and    R j  is selected from halo, hydroxy, methyl or methoxy.    
     
     
         22 . The method according to  claim 18  wherein q is 0 or 1.  
     
     
         23 . The method according to  claim 18  wherein q is 1 and R 2  is para to the —NH— of the aniline of formula (I).  
     
     
         24 . The method according to  claim 18  wherein R 3  is halo.  
     
     
         25 . The method according to  claim 18  wherein n is 0.  
     
     
         26 . The method according to  claim 18  wherein R 4  may be optionally substituted on carbon by one or more R d ; wherein R d  is selected from halo, amino, C 1-6 alkoxy, C 1-6 alkanoylamino, C 1-6 alkylsulphonylamino, phenyl or heterocyclic group.  
     
     
         27 . The method according to  claim 18  wherein R 5  and R 6  are independently selected from hydrogen or C 1-6 alkyl; wherein R 5  and R 6  independently of each other may be optionally substituted on carbon by one or more R e ; wherein R e  is selected from halo or methoxy.  
     
     
         28 . The method according to  claim 18  wherein: 
 R 1  is chloro, amino, methyl or methoxy;    p is 0-2; wherein the values of R 1  may be the same or different;    R 2  is sulphamoyl, N-(tetrahydrofur-2-ylmethyl)sulphamoyl, N-(cyclopropylmethyl)sulphamoyl, N-(fur-2-ylmethyl)sulphamoyl, N-(2,2-dimethyl-1,3-dioxolan-4-ylmethyl)sulphamoyl, N-(cyanomethyl)sulphamoyl, N-(carbamoylmethyl)sulphamoyl, N-methylsulphamoyl, N-(4-fluorobenzyl)sulphamoyl, N-(pyridin-2-ylmethyl)sulphamoyl, N-(pyridin-3-ylmethyl)sulphamoyl, N-(4-methylthiazol-2-yl)sulphamoyl, N-(3-methylisoxazol-5-ylmethyl)sulphamoyl, N-(tetrahydropyran-2-ylmethyl)sulphamoyl, N-(2-methylpyrazin-5-yl)sulphamoyl, N-[2-(2-hydroxyethoxy)ethyl]sulphamoyl, N-(2-hydroxyethyl)sulphamoyl, N-(2,2,2-trifluoroethyl)sulphamoyl, N-(2-methoxyethyl)sulphamoyl, N-(2-mesylethyl)sulphamoyl, N-(2-benzyloxyethyl)sulphamoyl, N-(2,2-dimethoxyethyl)sulphamoyl, N-[2-(N,N-dimethylamino)ethyl]sulphamoyl, N-(2-piperidin-1-ylethyl)sulphamoyl, N-[2-(methoxymethoxy)ethyl]sulphamoyl, N-ethylsulphamoyl, N-[2-(2-methoxyethoxy)ethyl]sulphamoyl, N-{2-[2-(2-methoxyethoxy)ethoxy]ethyl}sulphamoyl, N-(2-{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}ethyl)sulphamoyl, N-(2-pyridin-2-ylethyl)sulphamoyl, N-(2-pyridin-4-ylethyl)sulphamoyl, N-(2-isoxazol-3-yloxyethyl)sulphamoyl, N-(2-isothiazol-3-yloxyethyl)sulphamoyl, N-(2-1,2-5-thiadiazol-3-yloxyethyl)sulphamoyl, N-methyl-N-(2-methoxyethyl)sulphamoyl, N-[3-(2-oxopyrrolidin-1-yl)propyl]sulphamoyl, N-(3-methoxypropyl)sulphamoyl, N-propylsulphamoyl, N-(2,3-dihydroxypropyl)sulphamoyl, N-(3-morpholinopropyl)sulphamoyl, N-[3-(N,N-dimethylamino)propyl]sulphamoyl, N-(3,3,3-trifluoropropyl)sulphamoyl, N-(2,2-dimethyl-3-hydroxypropyl)sulphamoyl, N-(3-hydroxypropyl)sulphamoyl, N-(3-ethoxypropyl)sulphamoyl, N-(2-hydroxypropyl)sulphamoyl, N-(3-isopropoxypropyl)sulphamoyl, N-(3-isopropoxy-2-hydroxypropyl)sulphamoyl, N-(3-isoxazol-3-yloxypropyl)sulphamoyl, N-(3-isothiazol-3-yloxypropyl)sulphamoyl, N-(3-1,2-5-thiadiazol-3-yloxypropyl)sulphamoyl, N-(1,1-dimethylpropyl)sulphamoyl, N-methyl-N-(3-morpholinopropyl)sulphamoyl, N-butylsulphamoyl, N-t-butylsulphamoyl, N-(2-hydroxybutyl)sulphamoyl, N-methyl-N-t-butylsulphamoyl, N-pentylsulphamoyl, N-(5-hydroxypentyl)sulphamoyl, N-(4,5-dimethyloxazol-2-yl)sulphamoyl, N-(cyclopropyl)sulphamoyl, N-(cyclobutyl)sulphamoyl, N-(3-trifluoromethylphenyl)sulphamoyl, N-allylsulphamoyl, N-(2-propynyl)sulphamoyl, N-methylcarbamoyl, acetamido, mesylamino or mesyl;    q is 0 or 1;    R 3  is bromo or chloro;    n is 0 or 1;    R 4  is hydrogen, methyl, ethyl, isopropyl, 3-butenyl, benzyl, 2-phthalimidoethyl, 2-aminoethyl, 2-methoxyethyl, 2-acetamidoethyl, 2-mesylaminoethyl or 2,2,2-trifluoroethyl; and    R 5  and R 6  are independently selected from hydrogen, methyl, ethyl, isopropyl, trifluoromethyl or methoxymethyl.    
     
     
         29 . The method according to  claim 18  wherein the compound of formula (I) is selected from: 
 2-{4-[N-(cyclopropylmethyl)sulphamoyl]anilino}-4-(1,2-dimethylimidazol-5-yl)pyrimidine;    4-(1-ethyl-2-methylimidazol-5-yl)-2-{4-[N-(2-methoxyethyl)sulphamoyl]anilino}pyrimidine;    4-(1-ethyl-2-methylimidazol-5-yl)-2-{4-[N-(3-methoxypropyl)sulphamoyl]anilino}pyrimidine;    4-(1-ethyl-2-methylimidazol-5-yl)-2-{4-[N-(cyclopropylmethyl)sulphamoyl]anilino}pyrimidine;    4-(1-ethyl-2-methylimidazol-5-yl)-2-[4-(N-cyclopropylsulphamoyl)anilino]pyrimidine;    4-(1-methyl-2-isopropylimidazol-5-yl)-2-{4-[N-(cyclopropylmethyl)sulphamoyl]anilino}pyrimidine;    4-(1,2-dimethylimidazol-5-yl)-2-[4-(N-cyclopropylsulphamoyl)anilino]pyrimidine;    4-(1,2-dimethylimidazol-5-yl)-2-[4-(N-cyclobutylsulphamoyl)anilino]pyrimidine;    4-(1,2-dimethylimidazol-5-yl)-2-{4-[N-(2,2,2-trifluoroethyl)sulphamoyl]anilino}pyrimidine; and    4-(1-isopropyl-2-methylimidazol-5-yl)-2-[4-(N-cyclobutylsulphamoyl)anilino]pyrimidine;    or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof.