Aryl dihydropyridinones and piperidinone mgat2 inhibitors

Abstract

The present invention provides compounds of Formula (I):or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein all of the variables are as defined herein. These compounds are monoacylglycerol acyltransferase type 2 (MGAT2) inhibitors which may be used as medicaments.

What is claimed is: 
     
         1 . A compound of Formula (II): 
       
         
           
           
               
               
           
         
         or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof, wherein:
 R 1  is C 1-6  alkyl; 
 R 2  is independently selected from the group consisting of: C 1-4  alkyl and C 1-4  haloalkyl; 
 R 3  is independently selected from the group consisting of: H and F; 
 R 4  is independently selected from the group consisting of: H and F; 
 R 6  is independently R or —(CH 2 ) n —(X) t —(CH 2 ) m R c ; 
 X is independently selected from the group consisting of: O, S, NH, CONH, and NHCO; 
 R 11  and R 15  are independently selected from the group consisting of: H, C 1-4  alkyl and halo; 
 R 12  and R 14  are independently selected from the group consisting of: H, halo, C 1-4  alkyl and C 1-4  alkoxy; 
 R 13  is independently selected from the group consisting of: H, halo, C 1-4  alkyl substituted with 0-1 C 1-4  alkoxy, C 1-4  alkoxy, C 1-4  haloalkyl, C 1-4  haloalkoxy, —(CH 2 ) m —C 3-4  cycloalkyl, CN, N(C 1-4  alkyl) 2 , NHCO 2 (C 1-4  alkyl), NHSO 2 (C 1-4  alkyl), pyrazolyl, and morpholinyl; 
 alternatively, R 12  and R 13 , together with the carbon atoms to which they are attached, combine to form a 5- to 6-membered carbocyclic ring or a 5- to 6-membered heterocyclic ring comprising: carbon atoms and 1-3 heteroatoms selected from N, NR e , O, and S; 
 R c  is, at each occurrence, independently selected from the group consisting of: C 3-6  cycloalkyl substituted with 0-2 R d , C 3-6  cycloalkenyl substituted with 0-2 R d , —(CH 2 ) m -(phenyl substituted with 0-3 R d ), and a 5- to 6-membered heterocycle comprising: carbon atoms and 1-4 heteroatoms selected from N, NR e , O, and S; wherein said heterocycle is substituted with 0-2 R d ; 
 R d  is, at each occurrence, independently selected from the group consisting of: halo, OH, CN, NO 2 , C 1-4  alkyl, C 1-4  alkoxy, C 1-4  haloalkyl, C 1-4  haloalkoxy, tetrazolyl, OBn and phenyl substituted with 0-2 R h ; 
 R e  is, at each occurrence, independently selected from the group consisting of: H, C 1-8  alkyl, C 1-8  haloalkyl, benzyl optionally substituted with C 1-4  alkoxy, CO(C 1-4  alkyl) and COBn; 
 R h  is independently selected from the group consisting of: halo, C 1-4  alkyl, C 1-4  alkoxy, C 1-4  haloalkyl, and C 1-4  haloalkoxy; 
 n, at each occurrence, is independently 0 or 1; 
 m, at each occurrence, is independently 0, 1, 2 or 3; 
 s, at each occurrence, is independently 1, 2, or 3; and 
 t, at each occurrence, is independently 0 or 1. 
 
       
     
     
         2 . A compound according to  claim 1 , wherein:
 R 6  is independently R, OR, —CONHR c , or —NHCOR c ;   R 12  is independently selected from the group consisting of: H, halo, C 1-4  alkyl and C 1-4  alkoxy;   R 13  is independently selected from the group consisting of: H, halo, C 1-4  alkyl substituted with 0-1 C 1-4  alkoxy, C 1-4  alkoxy, C 1-4  haloalkyl, C 1-4  haloalkoxy, —(CH 2 ) m —C 3-4  cycloalkyl, CN, N(C 1-4  alkyl) 2 , NHCO 2 (C 1-4  alkyl), NHSO 2 (C 1-4  alkyl), pyrazolyl, and morpholinyl;   alternatively, R 12  and R 13 , together with the carbon atoms to which they are attached, combine to form a 5- to 6-membered carbocyclic ring or a 5- to 6-membered saturated heterocyclic ring comprising: carbon atoms and 1-2 oxygen atoms;   R 14  is independently selected from the group consisting of: H and C 1-4  alkoxy; and   R c  is, at each occurrence, independently selected from the group consisting of: C 3-6  cycloalkyl substituted with 0-2 R d , —(CH 2 ) m -(phenyl substituted with 0-3 R d ), and a heteroaryl selected from: oxazolyl, isoxazolyl, thiazolyl, pyrazolyl, imidazolyl, oxadiazolyl, triazolyl, tetrazolyl, pyridyl, and pyrazinyl; wherein said heteroaryl is substituted with 0-2 R d .   
     
     
         3 . A compound according to  claim 2 , wherein:
 R 6  is independently selected from the group consisting of: OPh, —CONH(C 3-6  cycloalkyl), —CONHPh, —CONH-(2-halo-Ph), —CONH-(3-halo-Ph), —CONH-(4-halo-Ph), —CONH-(4-C 1-4  alkyl-Ph), —CONH(4-OH-Ph), —CONH-(3-C 1-4  alkoxy-Ph), —CONH-(4-C 1-4  alkoxy-Ph), —CONH-(4-C 1-4  haloalkyl-Ph), —CONH-(4-C 1-4  haloalkoxy-Ph), —CONH-(4-CN-Ph), —CONH-(4-tetrazolyl-Ph), —CONH-(3-halo-4-C 1-4  alkyl-Ph), —CONH-(3-halo-4-C 1-4  alkoxy-Ph), —CONH(CH 2 ) 2 Ph, —CONH(4-(4-C 1-4  alkoxy-Ph)-thiazol-2-yl), —CONH(1-C 1-4  alkyl-pyrazol-3-yl), —CONH(5-C 1-4  alkoxy-pyrid-2-yl), —CONH(6-C 1-4  alkoxy-pyrid-3-yl), —CONH(5-C 1-4  alkoxy-pyrazin-2-yl), —CONH(6-C 1-4  alkoxy-pyridazin-3-yl), —NHCO(CH 2 )SO 2 (C 1-4  alkyl), —NHCOPh, —NHCO(2-C 1-4  alkyl-Ph), —NHCO(3-C 1-4  alkyl-Ph), —NHCO(4-C 1-4  alkyl-Ph), —NHCO(2-halo-Ph), —NHCO(3-halo-Ph), —NHCO(2-C 1-4  haloalkyl-Ph), —NHCO(2-C 1-4  haloalkoxy-Ph), —NHCO(2-halo-4-halo-Ph), —NHCO(2-halo-5-halo-Ph), —NHCO(oxazolyl), —NHCO(isoxazolyl), —NHCO(3-C 1-4  alkyl-isoxazol-5-yl), —NHCO(4-C 1-4  alkyl-isoxazol-5-yl), —NHCO(3-C 1-4  alkoxy-isoxazol-5-yl), —NHCO(4-C 1-4  alkoxy-isoxazol-5-yl), —NHCO(3-halo-isoxazol-5-yl), —NHCO(3-OBn-isoxazol-5-yl), —NHCO(3-(2-halo-Ph)-isoxazol-5-yl), —NHCO(3-(3-halo-Ph)-isoxazol-5-yl), —NHCO(5-C 1-4  alkyl-1H-pyrazol-3-yl), imidazolyl, —NHCO(5-C 1-4  alkyl-1,3,4-oxadiazol-2-yl), —NHCO(1-C 1-4  alkyl-1,2,3-triazol-4-yl), —NHCO(6-C 1-4  alkoxy-pyrid-3-yl), —NHCO(pyrazinyl), —NHCO(6-halo-pyridazin-3-yl), 5-C 1-4  haloalkyl-1,3,4-oxadiazol-2-yl, 3-NO 2 -1H-1,2,4-triazol-1-yl, tetrazolyl and 5-C 1-4  alkyl-tetrazol-1-yl.   
     
     
         4 . A compound according to  claim 3 , wherein:
 R 2  is independently selected from the group consisting of: CF 3  and Me;   R 3  is independently selected from the group consisting of: H and F;   R 4  is independently selected from the group consisting of: H and F;   R 6  is independently selected from the group consisting of: OPh, —CONH(cyclopropyl), —CONH(cyclobutyl), —CONH(cyclopentyl), —CONH(cyclohexyl), —CONHPh, —CONH(4-F-Ph), —CONH(2-Cl-Ph), —CONH(4-Cl-Ph), —CONH(4-Me-Ph), —CONH(4-OH-Ph), —CONH(3-OMe-Ph), —CONH(4-OMe-Ph), —CONH(4-CF 3 -Ph), —CONH(4-OCF 3 -Ph), —CONH(1-Me-pyrazol-3-yl), —CONH(4-(1H-tetrazol-2-yl)-Ph), —CONH(4-(2H-tetrazol-5-yl)-Ph), —CONH(3-F-4-Me-Ph), —CONH(3-F-4-OMe-Ph), —CONH(CH 2 ) 2 Ph, —CONH(5-OMe-pyrid-2-yl), —CONH(6-OMe-pyrid-3-yl), —CONH(5-OMe-pyrazin-2-yl), —CONH(6-OMe-pyridazin-3-yl), —NHCO(CH 2 )SO 2 Me, —NHCOPh, —NHCO(2-Me-Ph), —NHCO(3-Me-Ph), —NHCO(4-Me-Ph), —NHCO(2-Cl-Ph), —NHCO(3-Cl-Ph), —NHCO(2-Cl-4-F-Ph), —NHCO(2-Cl-5-F-Ph), —NHCO(isoxazol-5-yl), —NHCO(3-Me-isoxazol-5-yl), —NHCO(4-Me-isoxazol-5-yl), —NHCO(3-OMe-isoxazol-5-yl), —NHCO(3-Br-isoxazol-5-yl), —NHCO(3-(2-Cl-Ph)-isoxazol-5-yl), —NHCO(3-(3-F-Ph)-isoxazol-5-yl), —NHCO(3-OBn-isoxazol-5-yl), 1H-imidazol-1-yl, —NHCO(5-Me-1,3,4-oxadiazol-2-yl), —NHCO(1-Me-1,2,3-triazol-4-yl), —NHCO(6-OMe-pyrid-3-yl), —NHCO(6-Cl-pyridazin-3-yl), 5-CF 3 -1,3,4-oxadiazol-2-yl, 1H-tetrazol-1-yl, 1H-tetrazol-3-yl, and 2H-tetrazol-5-yl;   R 11  and R 15  are independently selected from the group consisting of: H, Me, F, and Cl;   R 12  is independently selected from the group consisting of: H, F, Cl, Me and OMe;   R 13  is independently selected from the group consisting of: H, F, Cl, Br, Me, OMe, OEt, CH 2 OMe, CF 3 , CH 2 CF 3 , OCHF 2 , OCF 3 , CN, N(Me) 2 , cyclopropyl and cyclopropylmethyl;   alternatively, R 12  and R 13 , together with the carbon atoms to which they are attached, combine to form a 5- to 6-membered carbocyclic ring or a 5- to 6-membered saturated heterocyclic ring comprising: carbon atoms and 1-2 oxygen atoms; and   R 14  is H.   
     
     
         5 . A compound according to  claim 2 , wherein:
 R 13  is independently selected from the group consisting of: H, halo, C 1-4  alkyl substituted with 0-1 C 1-4  alkoxy, C 1-4  alkoxy, C 1-4  haloalkyl, C 1-4  haloalkoxy, CN or C 3-4  cycloalkyl.   
     
     
         6 . A compound according to  claim 6 , wherein:
 R 6  is independently 5-membered nitrogen heteroaryl.   
     
     
         7 . A compound according to  claim 8 , wherein:
 R 6  is independently 1H-imidazol-1-yl, 1H-tetrazol-1-yl, 1H-tetrazol-3-yl, or 2H-tetrazol-5-yl.   
     
     
         8 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a compound of  claim 1 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof. 
     
     
         9 . The pharmaceutical composition according to  claim 8 , further comprising one or more other suitable therapeutic agents selected from: anti-diabetic agents, anti-hyperglycemic agents, anti-hyperinsulinemic agents, anti-retinopathic agents, anti-neuropathic agents, anti-nephropathic agents, anti-atherosclerotic agents, anti-ischemic agents, anti-hypertensive agents, anti-obesity agents, anti-dyslipidemic agents, anti-hyperlipidemic agents, anti-hypertriglyceridemic agents, anti-hypercholesterolemic agents, anti-restenotic agents, lipid lowering agents, anorectic agents, and appetite suppressants. 
     
     
         10 . A method for the treatment of diabetes, hyperglycemia, impaired glucose tolerance, gestational diabetes, insulin resistance, hyperinsulinemia, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, retinopathy, neuropathy, nephropathy, delayed wound healing, Metabolic Syndrome, obesity, dyslipidemia, and glaucoma, comprising administering to a patient in need of such treatment a therapeutically effective amount of at least a compound of  claim 1 . 
     
     
         11 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a compound of  claim 4 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof. 
     
     
         12 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a compound of  claim 5 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof. 
     
     
         13 . The pharmaceutical composition according to  claim 12 , further comprising one or more other suitable therapeutic agents selected from: anti-diabetic agents, anti-hyperglycemic agents, anti-hyperinsulinemic agents, anti-retinopathic agents, anti-neuropathic agents, anti-nephropathic agents, anti-atherosclerotic agents, anti-ischemic agents, anti-hypertensive agents, anti-obesity agents, anti-dyslipidemic agents, anti-hyperlipidemic agents, anti-hypertriglyceridemic agents, anti-hypercholesterolemic agents, anti-restenotic agents, lipid lowering agents, anorectic agents, and appetite suppressants. 
     
     
         14 . A method for the treatment of diabetes, hyperglycemia, impaired glucose tolerance, gestational diabetes, insulin resistance, hyperinsulinemia, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, retinopathy, neuropathy, nephropathy, delayed wound healing, Metabolic Syndrome, obesity, dyslipidemia, and glaucoma, comprising administering to a patient in need of such treatment a therapeutically effective amount of at least a compound of  claim 5 . 
     
     
         15 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a compound of  claim 6 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof. 
     
     
         16 . The pharmaceutical composition according to  claim 15 , further comprising one or more other suitable therapeutic agents selected from: anti-diabetic agents, anti-hyperglycemic agents, anti-hyperinsulinemic agents, anti-retinopathic agents, anti-neuropathic agents, anti-nephropathic agents, anti-atherosclerotic agents, anti-ischemic agents, anti-hypertensive agents, anti-obesity agents, anti-dyslipidemic agents, anti-hyperlipidemic agents, anti-hypertriglyceridemic agents, anti-hypercholesterolemic agents, anti-restenotic agents, lipid lowering agents, anorectic agents, and appetite suppressants. 
     
     
         17 . A method for the treatment of diabetes, hyperglycemia, impaired glucose tolerance, gestational diabetes, insulin resistance, hyperinsulinemia, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, retinopathy, neuropathy, nephropathy, delayed wound healing, Metabolic Syndrome, obesity, dyslipidemia, and glaucoma, comprising administering to a patient in need of such treatment a therapeutically effective amount of at least a compound of  claim 6 . 
     
     
         18 . A pharmaceutical composition, comprising: a pharmaceutically acceptable carrier and a compound of  claim 7 , or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt thereof. 
     
     
         19 . The pharmaceutical composition according to  claim 18 , further comprising one or more other suitable therapeutic agents selected from: anti-diabetic agents, anti-hyperglycemic agents, anti-hyperinsulinemic agents, anti-retinopathic agents, anti-neuropathic agents, anti-nephropathic agents, anti-atherosclerotic agents, anti-ischemic agents, anti-hypertensive agents, anti-obesity agents, anti-dyslipidemic agents, anti-hyperlipidemic agents, anti-hypertriglyceridemic agents, anti-hypercholesterolemic agents, anti-restenotic agents, lipid lowering agents, anorectic agents, and appetite suppressants. 
     
     
         20 . A method for the treatment of diabetes, hyperglycemia, impaired glucose tolerance, gestational diabetes, insulin resistance, hyperinsulinemia, nonalcoholic fatty liver disease, nonalcoholic steatohepatitis, retinopathy, neuropathy, nephropathy, delayed wound healing, Metabolic Syndrome, obesity, dyslipidemia, and glaucoma, comprising administering to a patient in need of such treatment a therapeutically effective amount of at least a compound of  claim 7 .