Di(arylamino)aryl compound

Abstract

The present invention provides a compound which is useful as an inhibitor against the kinase activity of EML4-ALK fusion proteins and mutant EGFR proteins. As a result of extensive and intensive studies on compounds having an inhibitory effect against the kinase activity of EML4-ALK fusion proteins and mutant EGFR proteins, the inventors of the present invention have found that the di(arylamino)aryl compound of the present invention has inhibitory activity against the kinase activity of EML4-ALK fusion proteins and mutant EGFR proteins. This finding led to the completion of the present invention. The compound of the present invention can be used as a pharmaceutical composition for preventing and/or treating cancer, lung cancer, non-small cell lung cancer, small cell lung cancer, EML4-ALK fusion polynucleotide-positive and/or mutant EGFR polynucleotide-positive cancer, EML4-ALK fusion polynucleotide-positive and/or mutant EGFR polynucleotide-positive lung cancer, or EML4-ALK fusion polynucleotide-positive and/or mutant EGFR polynucleotide-positive non-small cell lung cancer, etc.

1 - 18 . (canceled) 
     
     
         19 . A method for preventing or treating cancer, lung cancer, non-small cell lung cancer, small cell lung cancer, EML4-ALK fusion polynucleotide-positive and/or mutant EGFR polynucleotide-positive cancer, EML4-ALK fusion polynucleotide-positive and/or mutant EGFR polynucleotide-positive lung cancer, or EML4-ALK fusion polynucleotide-positive and/or mutant EGFR polynucleotide-positive non-small cell lung cancer, which comprises administering an effective amount of a compound of formula (I) or a salt thereof to a patient: 
       
         
           
           
               
               
           
         
       
       wherein:
 —X— represents 
 (1) a group of formula (II), or 
 (2) a group of formula (III) 
 
       
         
           
           
               
               
           
         
         —R 5  represents 
         (1) —H, 
         (2) —OH, 
         (3) halogen, 
         (4) lower alkyl which may be substituted with one or more halogens, 
         (5) O-lower alkyl which may be substituted with one or more halogens, 
         (6) —S-lower alkyl, 
         (7) cyano, 
         (8) amino which may be substituted with one or two lower alkyls, or 
         (9) cyclic amino which may be substituted with one or more groups selected from the group consisting of lower alkyl, oxo, —OH, —O-lower alkyl, and amino which may be substituted with one or two lower alkyls (provided that the triazine ring to which —R 5  is attached is attached to the nitrogen atom in the cyclic amino), 
         —R 6a , —R 6b , —R 6c  and —R 6d , K which may be the same or different, each represent 
         (1) —H, 
         (2) halogen, 
         (3) lower alkyl which may be substituted with one or more halogens, 
         (4) O-lower alkyl which may be substituted with one or more halogens, 
         (5) —S-lower alkyl, or 
         (6) cyano, 
         —W represents 
         a group represented by -A-B, 
         -A- is —S(═O) 2 —, 
         -B is isopropyl, 
         —R 1a , —R 1b , —R 1c  and —R 1d  are each —H, —R 2  is —O-methyl, —R 4  is —H, and —R 3  is 4-(4-methylpiperazin-1-yl)piperidin-1-yl. 
       
     
     
         20 . The method according to claim  1 , wherein —X— is a group represented by formula (II) and —R 5  is —H. 
     
     
         21 . The method according to claim  1 , wherein said compound is N 4 -[2-(isopropylsulfonyl)phenyl]-N 2 -{2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}quinazoline-2,4-diamine. 
     
     
         22 . The method according to claim  1 , wherein said compound is N-[2-(isopropylsulfonyl)phenyl]-N-{2-methoxy-4-[4-(4-methylpiperazin-1-yl)piperidin-1-yl]phenyl}-1,3,5-triazine-2,4-diamine.