Thieno- and furo - pyrimidines and pyridines, useful as potassium channel inhibitors

Abstract

The present invention provides compounds of formula (I): (Formula (I)); wherein A, R 1 , R 2 , R 3 I , V, X, and Z are defined herein, which are potassium channel inhibitors. The invention further provides pharmaceutical compositions comprising the compounds of formula (I) and their use in therapy, in particular in treatment of diseases or conditions that are mediated by K ir 3.1 and/or K ir 3.4 or any heteromultimers thereof, or that require inhibition of K ir 3.1 and/or K ir 3.4 or any heteromultimers thereof.

1 . A compound of formula (I) 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable derivative thereof, wherein:
 A is S; 
 X is CR 3   II ; 
 V is CR 3   III ; 
 Z is N; 
 R 1  is selected from optionally substituted alkyl, optionally substituted cycloalkyl, optionally substituted aryl, and optionally substituted heteroaryl; 
 R 2  is selected from H, halo, —CN, trifluoromethyl, optionally substituted alkyl, optionally substituted alkoxy, —NR 4 R 5 , —NR 6 C(O)R 7 , —NR 6 S(O) 2 R 7 , —S(O) 2 NR 4 R 5 , —CONR 4 R 5 , —CO 2 R 7 , optionally substituted oxazolinyl, —SR 14 , —S(O)R 14  and —S(O) 2 R 14 ; 
 R 3   I  is selected from H, halo, —CN, trifluoromethyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted heterocycloalkoxy, —NR 6 C(O)R 7 , —NR 6 S(O) 2 R 7 , —S(O) 2 NR 4 R 5 , —CONR 4 R 5 , —CO 2 R 7 , —NR 8 R 9 , —C≡C-J, optionally substituted cycloalkyl-J and —(NR a R b )-J; 
 Each of R 3   II  and R 3   III  is independently selected from H, halo, —CN, trifluoromethyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted heterocycloalkoxy, optionally substituted heterocycloalkylalkyl, —NR 6 C(O)R 7 , —NR 6 S(O) 2 R 7 , —S(O) 2 NR 4 R 5 , —CONR 4 R 5 , optionally substituted-alkylene-CONR 4 R 5 , —CO 2 R 7 , —NR 10 R 11 , —C≡C-J, optionally substituted cycloalkyl-J and —(NR c R d )-J, provided that R 3   I  is —C≡C-J, optionally substituted cycloalkyl-J or —(NR a R b )-J, and/or at least one of R 3   II  and R 3   III  is present as —C≡C-J, optionally substituted cycloalkyl-J or —(NR c R d )-J; 
 wherein R a  and R b  are linked to form an optionally substituted 4 to 7 membered heterocycloalkyl ring, which is optionally bridged by a bond, optionally substituted C 1-2 alkylene, —NR 6 —, —O—, or —S(O) z —, wherein the optionally bridged, optionally substituted heterocycloalkyl ring is selected from the group consisting of azetidinyl, pyrrolidinyl, piperidinyl, morpholinyl, tetrahydro-1,3-oxazinyl, hexahydropyrimidinyl, 1,4-thiazanyl, azepanyl, 1,4-oxaazepanyl, and 1,4-thieazepanyl; 
 wherein R c  and R d  are linked to form an optionally substituted 4 to 7 membered heterocycloalkyl ring, which is optionally bridged by a bond, optionally substituted C 1-2 alkylene, —NR 6 —, —O—, or —S(O) z —; 
 J is selected from H and —(CR 12 R 13 )q-L-M-W, 
 
         wherein
 q is 0, 1 or 2; 
 L is —O— or —N(G)-; and 
 G is selected from hydrogen, optionally substituted alkyl and optionally substituted cycloalkyl; 
 M is —(CR 12 R 13 ) t —; 
 t is 0, 1, 2 or 3; 
 W is selected from the group consisting of optionally substituted alkyl, optionally substituted alkoxy, optionally substituted alkenyl, optionally substituted cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted aryl, optionally substituted heteroaryl and —NR 8 R 9 , 
 wherein when W is optionally substituted cycloalkyl it may optionally be bridged by a bond or optionally substituted C 1-2 alkylene, and 
 wherein when W is optionally substituted heterocycloalkyl it may optionally be bridged by a bond, optionally substituted C 1-2 alkylene, —NR 6 —, —O—, or —S(O) z —; 
 alternatively, when L=—N(G)-, L, G, M and W may be linked to form an optionally substituted heterocycloalkyl, an optionally substituted heterocycloalkenyl, or an optionally substituted heteroaryl; 
 z is 0, 1 or 2; 
 R 4  and R 5  are, at each instance, independently selected from H, optionally substituted alkyl, optionally substituted aryl, optionally substituted heteroaryl, and optionally substituted cycloalkyl, or are linked to form an optionally substituted heterocycloalkyl; 
 R 6  and R 7  are, at each instance, independently selected from H and optionally substituted alkyl, or are linked to form an optionally substituted heterocycloalkyl; 
 R 8  and R 9  are, at each instance, independently selected from optionally substituted alkyl, optionally substituted aryl, optionally substituted heterocycloalkyl, optionally substituted heteroaryl, and optionally substituted cycloalkyl; 
 R 10  and R 11  are, at each instance, independently selected from H, optionally substituted alkyl, optionally substituted aryl, optionally substituted heterocycloalkyl, optionally substituted heteroaryl, and optionally substituted cycloalkyl; 
 R 12  and R 13  are, at each instance, independently selected from H, hydroxy, and optionally substituted alkyl, or may be linked to form an optionally substituted cycloalkyl ring, or may together form ═O; and 
 R 14  is optionally substituted alkyl, 
 wherein the optional substituents are independently selected from halo, trihalomethyl, trihaloethyl, trihalomethoxy, trihaloethoxy, —OH, —NO 2 , —CN, —CO 2 H, —CO 2 C 1-6 alkyl, —SO 3 H, —SOC 1-6 alkyl, —SO 2 C 1-6 alkyl, —NHSO 2 C 1-6 alkyl, —NC 1-6 alkylSO 2 C 1-6 alkyl, —SO 2 NH 2 , —SO 2 NHC 1-6 alkyl, —SO 2 N(C 1-6 alkyl) 2 , —NHSO 2 NH 2 , —NHSO 2 NHC 1-6 alkyl, —NHSO 2 N(C 1-6 alkyl) 2 , —NC 1-6 alkylSO 2 NH 2 , —NC 1-6 alkylSO 2 NHC 1-6 alkyl, —NC 1-6 alkylSO 2 N(C 1-6 alkyl) 2 , —C(═O)H, —C(═O)C 1-6 alkyl, —NHC(═O)C 1-6 alkyl, —NC 1-6 alkylC(═O)C 1-6 alkyl, C 1-6 alkylenedioxy, ═θO, —N(C 1-6 alkyl) 2 , —C(═O)NH 2 , —C(═O)NHC 1-6 alkyl, —C(═O)N(C 1-6 alkyl) 2 , —NHC(═O)NH 2 , —NHC(═O)NHC 1-6 alkyl, —NHC(═O)N(C 1-6 alkyl) 2 , —NC 1-6 alkylC(═O)NH 2 , —NC 1-6 alkylC(═O)NHC 1-6 alkyl, —NC 1-6 alkylC(═O)N(C 1-6 alkyl) 2 , —C(═NH)NH 2 , —C(═NH)NHC 1-6 alkyl, —C(═NH)N(C 1-6 alkyl) 2 , —C(═NC 1-6 alkyl)NH 2 , —C(═NC 1-6 alkyl)NHC 1-6 alkyl, —C(═NC 1-6 alkyl)N(C 1-6 alkyl) 2 , —C 1-6 alkyl, —C 3-6 cycloalkyl, —C 3-6 heterocycloalkyl, 2-imidazolidinon-3-yl, 1-C 1-6 alkyl-2-imidazolidinon-3-yl, C 1-6 alkylC 3-6 heterocycloalkyl, aryl, haloaryl, C 1-6 alkoxyaryl, —C 1-6 alkylene-NHSO 2 C 1-6 alkyl, —C 1-6 alkylene-NC 1-6 alkylSO 2 C 1-6 alkyl, —C 1-6 alkylene-SO 2 NH 2 , —C 1-6 alkylene-SO 2 NHC 1-6 alkyl, —C 1-6 alkylene-SO 2 N(C 1-6 alkyl) 2 , —Z t H, —Z t —C 1-6 alkyl, —C 1-6 alkylene-Z t H, —Z t —C 3-6 cycloalkyl, or —C(═O)NHC 1-6 alkylene-Z t H wherein Z t  is independently O, S, NH or N(C 1-6 alkyl). 
 
       
     
     
         2 . The compound of  claim 1 , wherein R 1  is phenyl. 
     
     
         3 . The compound of  claim 1 , wherein R 2  is selected from H, trifluoromethyl, substituted alkyl, optionally substituted alkoxy, —NR 4 R 5 , —NR 6 C(O)R 7 , —S(O) 2 NR 4 R 5 , —CONR 4 R 5 , CO 2 R 7 , optionally substituted oxazolinyl, —SR 14 , —S(O)R 14  and —S(O) 2 R 14 . 
     
     
         4 . The compound of  claim 1 , wherein R 3   I  is selected from trifluoromethyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted heterocycloalkoxy, —NR 6 C(O)R 7 , —NR 6 S(O) 2 R 7 , —S(O) 2 NR 4 R 5 , —CONR 4 R 5 , —CO 2 R 7 , —NR 8 R 9 , optionally substituted cycloalkyl-J and —(NR a R b )-J. 
     
     
         5 . The compound of  claim 1 , wherein R 3   III  is selected from H, halo, —CN, trifluoromethyl, optionally substituted alkyl, optionally substituted alkoxy, optionally substituted heterocycloalkoxy, optionally substituted heterocycloalkylalkyl, —NR 6 C(O)R 7 , —NR 6 S(O) 2 R 7 , —S(O) 2 NR 4 R 5 , —CONR 4 R 5 , optionally substituted-alkylene-CONR 4 R 5 , —CO 2 R 7 , —NR 10 R 11 , optionally substituted cycloalkyl-J and —(NR c R d )-J. 
     
     
         6 . The compound of  claim 1 , wherein R 3   I  is —(NR a R b )-J. 
     
     
         7 . The compound of  claim 1 , wherein R 3   I  is —(NR a R b )-J, V is CR 3   III  and R 3   III  is H or —(NR c R d )-J and, in at least one instance, J is —(CR 12 R 13 )q-L-M-W. 
     
     
         8 . The compound of  claim 1 , wherein q is 0 or 1. 
     
     
         9 . The compound of  claim 1 , wherein q is 1. 
     
     
         10 . The compound of  claim 1 , wherein t is 0, 1 or 2. 
     
     
         11 . The compound of  claim 1 , wherein t is 2. 
     
     
         12 . The compound of  claim 1 , wherein L is O. 
     
     
         13 . The compound of  claim 1 , wherein L is —N(G)-. 
     
     
         14 . The compound of  claim 1 , wherein R 12  and R 13  are, at each instance, H. 
     
     
         15 . The compound of  claim 1 , wherein W is optionally substituted heterocycloalkyl. 
     
     
         16 . A pharmaceutical composition comprising at least one compound as claimed in  claim 1  and, optionally, one or more pharmaceutically acceptable excipients. 
     
     
         17 . A method for the treatment of a disease or condition that is mediated by K ir 3.1 and/or K ir 3.4 or any heteromultimers thereof, or that requires inhibition of K ir 3.1 and/or K ir 3.4 or any heteromultimers thereof, comprising administering to a subject an effective amount of at least one compound of formula (I) as defined in  claim 1   or a composition comprising at least one compound of formula (I) as defined in  claim 1  and, optionally, one or more pharmaceutically acceptable excipients.   
     
     
         18 . The method of  claim 17 , wherein the method is for the treatment of cardiovascular diseases, such as atrial fibrillation (AF), atrial flutter (AFL), atrioventricular (AV) dysfunction and sinoatrial node (SAN) dysfunction; the prevention of recurrence of supraventricular arrhythmias including AF and AFL; the maintenance of sinus rhythm; the termination and cardioversion of supraventriclar arrhythmias; the treatment of sinus node dysfunction; the treatment of AV node dysfunction, including AV block; the treatment of conduction dysfunction; the prevention or reversal of atrial structural and ionic remodeling; the prevention of thrombosis, thromboembolism and thromboembolic diseases, such as stroke, myocardial infarction, and peripheral vascular diseases; the improvement of cardiac contractility; the treatment of metabolic diseases, such as diabetes mellitus; the modulation of neuro-endocrine function; the modulation of the secretion of pituitary hormones; the treatment of neurological and neuropsychiatric disorders, such as pain, depression, anxiety, attention deficit/hyperactivity disorder and epilepsy; and the treatment of cancer, such as breast cancer.