Bicyclic heteroaryl substituted compounds

Abstract

Disclosed are compounds of Formula (I) to (VIII): (I) (II) (III) (IV) (V) (VI) (VII) (VIII); or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate or prodrug thereof, wherein R3 is a bicyclic heteroaryl group substituted with zero to 3 R 3a ; and R 1 , R 2 , R 3a , R 4 , and n are defined herein. Also disclosed are methods of using such compounds as PAR4 inhibitors, and pharmaceutical compositions comprising such compounds. These compounds are useful in inhibiting or preventing platelet aggregation, and are useful for the treatment of a thromboembolic disorder or the primary prophylaxis of a thromboembolic disorder.

What is claimed is: 
     
         1 . A compound of Formula (I) to (VIII): 
       
         
           
           
               
               
           
         
         or a salt thereof; wherein:
 R 1  is F, Cl, —OH, C 1-4  alkyl, C 1-4  fluoroalkyl, C 2-4 alkenyl, C 2-4 alkynyl, C 3-7  cycloalkyl, C 3-7  fluorocycloalkyl, C 1-4  alkoxy, C 1-4  fluoroalkoxy, C 2-4  hydroxyalkoxy, C 3-6  cycloalkoxy, (C 1-3  alkoxy)-(C 1-3  alkylene), (C 1-3  alkoxy)-(C 1-3  fluoroalkylene), (C 1-3  deuteroalkoxy)-(C 1-3  deuteroalkylene), (C 1-3  fluoroalkoxy)-(C 1-3  alkylene), (C 1-3  fluoroalkoxy)-(C 1-3  fluoroalkylene), —(CH 2 ) 1-3 O(phenyl), —(CH 2 ) 1-3 NR a R a , —C(O)O(C 1-6  alkyl), —C(O)NR a R a , —C(O)NR b R b , —NH 2 , —NH(C 1-6  alkyl), —N(C 1-6  alkyl) 2 , —NH(C 1-6  hydroxyalkyl), azetidinyl, pyrrolidinyl, furanyl, pyranyl, piperidinyl, morpholinyl, piperazinyl, —S(O) 2 (C 1-3  alkyl), —S(O) 2 NR a R a , C 1-3  alkylthio, or C 1-3  fluoroalkylthio; 
 R 2 , at each occurrence, is independently H, F, Cl, Br, —OH, —CN, C 1-4  alkyl, C 1-4  fluoroalkyl, C 1-4  hydroxyalkyl, C 1-3  aminoalkyl, C 2-4  alkenyl, C 2-4  alkynyl, C 3-7  cycloalkyl, C 3-7  fluorocycloalkyl, C 1-6  alkoxy, C 1-3  fluoroalkoxy, C 1-3  alkylthio, C 1-3  fluoroalkylthio, (C 1-3  alkoxy)-(C 1-3  alkylene), (C 1-3  fluoroalkoxy)-(C 1-3  alkylene), —C(O)NH 2 , —C(O)NH(C 1-6  alkyl), —C(O)N(C 1-6  alkyl) 2 , —C(O)O(C 1-6  alkyl), —C(O)NH(CH 2 CH 2 O(C 1-3  alkyl)), —C(O)NR b R b , —C(O)(piperidinyl), —CH(OH)(C 3-6  cycloalkyl), —CH(OH)(phenyl), —CH(OH)(pyridyl), —S(O) 2 (C 1-3  alkyl), —S(O) 2 NR a R a , or a cyclic group selected from phenyl, 5-to 6-membered heteroaryl, and 5-to 7-membered heterocyclyl, wherein said cyclic group is substituted with zero to 5 substituents independently selected from F, Cl, hydroxy, C 1-3  alkyl, C 1-3  alkoxy, cyclopropyl, and —CN; 
 R 3  is a bicyclic group selected from indolyl, benzofuranyl, benzo[b]thiophenyl, benzo[d]imidazolyl, benzo[d]oxazolyl, benzo[d]thiazolyl, imidazol[1,2-a]pyridinyl, thiazolo[4,5-b]pyridinyl, thiazolo[4,5-c]pyridinyl, thiazolo[5,4-b]pyridinyl, thiazolo[5,4-c]pyridinyl, 4,5,6,7-tetrahydrobenzo[d]thiazolyl, 4,5,6,7-tetrahydrobenzofuranyl, 4,5,6,7-tetrahydrothiazolo[5,4-c]pyridinyl, 5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazolyl, 5,6-dihydro-4H-cyclopenta[d]thiazolyl, indolizinyl, pyrrolo[1,2-a]pyrimidinyl, 6,7-dihydrothiazolo[5,4-c]pyridinyl, 6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazinyl, 4,5,6,7-tetrahydrobenzothiophenyl, furo[3,2-b]pyridinyl, and furo[2,3-b]pyridinyl, each bicyclic group substituted with zero to 3 R 3a ; 
 R 3a , at each occurrence, is independently: 
 
         (i) F, Cl, —CN, —OH, C 1-3  alkyl, C 1-6  fluoroalkyl, C 1-6  hydroxyalkyl, C 1-6  hydroxy-deuteroalkyl, C 1-6  hydroxy-fluoroalkyl, C 1-6  alkoxy, C 1-3  fluoroalkoxy, C 3-6  cycloalkyl, C 3-6  fluorocycloalkyl, 4-to 7-membered heterocyclyl, —CH(OH)R y  wherein R y  is C 3-6  cycloalkyl, aryl, heteroaryl, or 4-to 7-membered heterocyclyl; (C 1-3  alkoxy)-(C 1-3  alkylene), —(CH 2 ) 1-3 NR a R a , —(CH 2 ) 1-3 NHS(O) 2 (aryl), —O(CH 2 ) 1-3 (aryl), —O(CH 2 ) 1-3 (thiazolyl), —O(CH 2 ) 1-3 (oxazolidinonyl), —O(CH 2 ) 1-3 (amino isoxazolyl), —O(CH 2 ) 1-3 (imidazolyl substituted with phenyl), C 1-6  hydroxyalkoxy, (C 1-3  alkoxy)-(C 1-6  alkoxy), —O(CH 2 ) 1-4 O(aryl), —O(CH 2 ) 1-4 O(CH 2 ) 1-3 (aryl), —O(CH 2 ) 1-4 NR a R a , —O(CH 2 ) 1-3 CHR a NR a (methoxy pyrimidinyl), —O(CH 2 ) 1-4 NHS(O) 2 (C 1-3  alkyl), —O(CH 2 ) 1-4 NHS(O) 2 (aryl), —O(CH 2 ) 1-4 C(O)OH, —O(CH 2 ) 1-4 C(O)O(C 1-6  alkyl), —O(CH 2 ) 1-4 C(O)NR a (CH 2 ) 0-3 (aryl), —O(CH 2 ) 1-4 C(O)NR a (CH 2 ) 0-3 (heteroaryl), —O(CH 2 ) 1-4 C(O)(morpholinyl), —O(CH 2 ) 1-4 OC(O)O(C 1-3  alkyl), —O(CH 2 ) 1-3 CHR a OC(O)NR a (CH 2 ) 1-4 C(O)NR a R a , —CH 2 CHR d OC(O)NR a (heteroaryl), —O(CH 2 ) 1-4 OC(O)NR a (heteroaryl), —O(imidazolyl substituted with aryl), —C(O)OH, —C(O)O(C 1-6  alkyl), —NR a C(O)(furanyl), —NR a C(O)(pyranyl), —NR a C(O)O(C 1-6  alkyl), —NR a C(O)O(CH 2 ) 1-4 (aryl), —O(CH 2 ) 1-4 NR a C(O)O(C 1-6  alkyl), —O(CH 2 ) 1-4 NR a C(O)O(CH 2 ) 0-4 (tetrahydropyranyl), —O(CH 2 ) 1-4 NR a C(O)O(CH 2 ) 0-4 (aryl), —O(CH 2 ) 1-4 NR a C(O)O(CH 2 ) 0-4 (heteroaryl), or —O(CH 2 ) 1-4 NR a C(O)O(CH 2 ) 0-4 (tetrahydrofuranyl), wherein each of said aryl, heteroaryl, and 3- to 6-membered heterocyclyl is substituted with zero to 5 substituents independently selected from F, Cl, —CN, C 1-3  alkyl, C 1-3  fluoroalkyl, C 1-4  hydroxyalkyl, C 1-3  alkoxy, —OCF 3 , —OCHF 2 , —NH 2 , —NH(C 1-6  alkyl), —N(C 1-6  alkyl) 2 , —C(O)O(C 1-3  alkyl), C 1-3  hydroxyalkoxy, phenyl, —CONR c R c , and —S(O) 2 NR c R c ; 
         (ii) —CH(OH)CR h R i R j  wherein R h  and R i  are independently H, F, C 1-4  alkyl, C 1-4  fluoroalkyl, C 1-3  alkoxy, C 1-3  fluoroalkoxy, or taken together with the carbon atom to which they are attached, form C 3-8  cycloalkyl or 4- to 7-membered heterocyclyl ring; and R j  is H, C 1-6  alkyl, C 1-5  fluoroalkyl, (C 1-3  alkoxy)-(C 1-3  alkylene), C 3-8  cycloalkyl, C 3-8  heterocyclyl, aryl, or heteroaryl; 
         (iii) —O(CH 2 ) 1-4 NR a S(O) 2 (C 1-4  alkyl) or —O(CH 2 ) 1-4 NR a S(O) 2 R w , wherein R w  is aryl or heteroaryl, each substituted with zero to 2 substituents independently selected from F, Cl, cyano, C 1-3  alkyl, C 1-3  alkoxy, —OCF 3 , —OCHF 2 , and C 1-3  fluoroalkyl; or 
         (iv) —O(CH 2 ) 1-4 OC(O)NR a R x , —OCH(R d )(CH 2 ) 1-3 OC(O)NR a R x , —OCR d R d (CH 2 ) 1-3 OC(O)NR a R x , —O(CH 2 ) 1-3 CH(R d )OC(O)NR a R x , —O(CH 2 ) 1-3 CR d R d OC(O)NR a R x , —OCH(R d )CH(R d )(CH 2 ) 0-2 OC(O)NR a R x , or —OCR d R d CR d R d (CH 2 ) 0-2 OC(O)NR a R x , wherein R x  is selected from H, C 1-4  alkyl, C 1-4  fluoroalkyl, aryl, heteroaryl, and —CH 2 (heteroaryl), each aryl and heteroaryl substituted with zero to 2 substituents independently selected from F, Cl, Br, —CN, —OH, C 1-3  alkyl, C 1-3  fluoroalkyl, C 1-6  hydroxyalkyl, C 1-6  hydroxy-deuteroalkyl, C 1-6  hydroxyalkoxy, C 1-6  hydroxy-fluoroalkoxy, C 1-3  alkoxy, —C(O)OH, —(CH 2 ) 0-3 C(O)O(C 1-3  alkyl), —(CH 2 ) 1-3 OP(O)(OH) 2 , —CH 2 (morpholinyl), —C(O)NH 2 , —C(O)NH(C 1-6  alkyl), —C(O)N(C 1-6  alkyl) 2 , —C(O)NR a (C 1-6  hydroxyalkyl), —C(O)NR b R b , —S(O) 2 NR a R a , —NH 2 , —NH(C 1-6  alkyl), —NR a (C 1-6  hydroxyalkyl), —N(C 1-6  alkyl) 2 , —NR a C(O)(C 1-6  alkyl), —NR a C(O)(chloro, fluorophenyl), —NR a S(O) 2 (C 1-3  alkyl), —C(O)NR a (CH 2 ) 0-1  (hydroxymethyloxetanyl), —C(O)NR a (CH 2 ) 0-1  (hydroxymethyl C 3-6  cycloalkyl), —C(O)NR a (CH 2 ) 0-1  (hydroxy C 3-6  cycloalkyl), —C(O)NHCH 2 C(CH 3 ) 2 OP(O)(OH) 2 , —C(O)(hydroxypiperidinyl), —C(O)(hydroxypyrrolidinyl), —C(O)(hydroxymethylpyrrolidinyl), —C(O)(morpholinyl), —C(O)(hydroxymethylmorpholinyl), pyrrolidinyl, morpholinyl, thiophenyl, methyl triazolyl, and oxazolidinonyl;
 R 4  is H, F, Cl, or —CH 3 ; 
 R a , at each occurrence, is independently H, C 1-4 alkyl, or C 1-4  fluoroalkyl; 
 two R b  along with the nitrogen atom to which they are attached form a 4- to 7-membered heterocyclo ring having 1 to 2 nitrogen atoms and 0-1 oxygen or sulfur atoms; 
 R c , at each occurrence, is independently C 1-3  alkyl or C 1-3  hydroxyalkyl, or two R c  along with the nitrogen atom to which they are attached form a heterocyclyl or bicyclic heterocyclyl; 
 R d , at each occurrence, is independently C 1-6  alkyl, C 1-4  fluoroalkyl, C 1-6  hydroxyalkyl, (C 1-4  alkoxy)-(C 1-3  alkylene), (C 1-2  fluoroalkoxy)-(C 1-2  alkylene), (C 3-6  cycloalkyl)-(C 0-2  alkylene), aryl-(C 1-2  alkylene), heteroaryl-(C 1-2  alkylene), aryloxy-(C 1-2  alkylene), aryl-CH 2 O—(C 1-2  alkylene), or heteroaryloxy-(C 1-2  alkylene); and 
 n is zero, 1, or 2. 
 
       
     
     
         2 . The compound according to  claim 1  having the structure of Formula (I) to Formula (IV): 
       
         
           
           
               
               
           
         
       
     
     
         3 . The compound according to  claim 1  or a salt thereof; wherein:
 R 1  is —OH, C 1-2  alkyl, —CHFCH 3 , —CH═CH 2 , C 1-3  alkoxy, C 1-2  fluoroalkoxy, —OCH 2 CH 2 OH, —CH 2 O(C 1-2  alkyl), —CD 2 OCD 3 , —CH 2 OCHF 2 , —CF 2 OCH 3 , —CH 2 O(phenyl), —CH(CH 3 )OCH 3 , —NH(CH 3 ), —N(CH 3 ) 2 , —CH 2 N(CH 3 ) 2 , —C(O)NH 2 , —C(O)NH(CH 3 ), —C(O)N(CH 3 ) 2 , —C(O)NH(CH 2 CH 2 OH), —C(O)OCH 3 , —CH(CH 3 )OCH 3 , cyclopropyl, furanyl, or —O(cyclopropyl); 
 R 2 , at each occurrence, is independently H, F, Cl, —CN, —CH 3 , —CH 2 F, —CHF 2 , —CF 3 , —OCH 3 , —OCF 3 , —CH 2 OH, —CH 2 CH 2 OH, —CH(CH 3 )OH, —C(CH 3 ) 2 OH, —CH(OH)CH 2 OH, —CH 2 NH 2 , —C(O)NH 2 , —C(O)N(CH 3 ) 2 , —C(O)(piperidinyl), —C(O)OCH 3 , —C(O)NH(CH 2 CH 2 OCH 3 ), —CH(OH)(cyclopropyl), —CH(OH)(phenyl), —CH═CH 2 , —C(CH 3 )═CH 2 , or —C≡CH; 
 R 3  is: 
 
       
         
           
           
               
               
           
         
       
       R 3a , at each occurrence, is independently:
 (i) F, Cl, —CN, —OH, —CH 3 , —CF 3 , —CHFC(CH 3 ) 3 , cyclopropyl, —CH 2 OH, —CD 2 OH, —CH 2 CH 2 OH, —CH(OH)CH 3 , —C(CH 3 ) 2 OH, —CH(OH)C(CH 3 ) 3 , —CD(OH)C(CH 3 ) 3 , —CH(OH)CF 3 , —CH(OH)CH 2 CF 3 , —CH(OH)(cyclopropyl), —CH(OH)(methylcyclopropyl), —CH(OH)(trifluoromethylcyclopropyl), —CH(OH)(cyclopropyl substituted with phenyl), —CH(OH)(cyclobutyl), —CH(OH)(methoxycyclobutyl), —CH(OH)(ethoxycarbonylcyclobutyl), —CH(OH)(trifluoromethylcyclobutyl), —CH(OH)(hydroxymethylcyclobutyl), —CH(OH)(cyclobutyl substituted with phenyl), —CH(OH)(cyclohexyl), —CH(OH)(methylcyclohexyl), —CH(OH)(phenyl), —CH(OH)(isopropylphenyl), —CH(OH)(trifluoromethylphenyl), —CH(OH)(fluoro, methoxyphenyl), —CH(OH)(pyridinyl), —CH(OH)(thiazolyl), —CH(OH)(tetrahydropyranyl), —CH(OH)(methyltetrahydropyranyl), —CH 2 OCH 3 , —CH 2 N(CH 3 ) 2 , —CH 2 NHS(O) 2 (phenyl), or —CH(OH)CH 2 (phenyl); 
 (ii) —OCH 3 , —OCH 2 CH 3 , —OCH(CH 3 ) 2 , —OCF 3 , —OCHF 2 , —OCH 2 (phenyl), —OCH 2 (thiazolyl), —OCH 2 (oxazolidinonyl), —OCH 2 (amino isoxazolyl), —OCH 2 (imidazolyl substituted with phenyl), —OCH 2 CH 2 OH, —OCH 2 CH(CH 3 )OH, —OCH 2 CH 2 OCH 3 , —OCH(CH 3 )CH 2 OH, —OCH 2 CH(OH)CH 3 , —OCH(CH 3 )CH(OH)CH 3 , —OCH 2 C(CH 3 ) 2 OH, —OCH 2 CH 2 O(phenyl), —OCH 2 CH 2 OCH 2 (phenyl), —OCH 2 CH 2 NH(CH 3 ), —OCH 2 CH(CH 3 )NH(methoxy pyrimidinyl), —OCH 2 C(O)OH, —OCH 2 C(O)OCH 3 , —OCH 2 C(O)OCH 2 CH 3 , —OCH 2 C(O)OC(CH 3 ) 3 , —OCH 2 C(O)NH(phenyl), —OCH 2 C(O)NHCH 2 (phenyl), —OCH 2 C(O)(morpholinyl), —OCH 2 CH 2 CH 2 C(O)NH(pyridinyl), —OCH 2 CH 2 OC(O)OCH 3 , —OCH 2 CH(CH 3 )OC(O)NHCH 2 CH 2 C(O)NH 2 , —OCH 2 CH(CH 2 CH 3 )OC(O)NH(pyridinyl), —OCH 2 CH(CH 2 OCH 3 )OC(O)NH(pyridinyl), —OCH 2 CH(CH 2 OC(CH 3 ) 3 )OC(O)NH(pyridinyl), —OCH 2 CH(CH 2 OCH 2 CH(CH 3 ) 2 )OC(O)NH(pyridinyl), —OCH 2 CH(CH 2 OCH 2 (phenyl))OC(O)NH(pyridinyl), —OCH 2 CH(CH 2 OCH 2 CH(CH 3 ) 2 )OC(O)NH(pyrimidinyl), or —OCH 2 CH(CH 2 OCH 2 CH(CH 3 ) 2 )OC(O)NH(methyl pyrimidinyl); 
 (iii) —C(O)OH, —C(O)OCH 3 , or —C(O)OC(CH 3 ) 3 ; 
 (iv) —NHC(O)OCH 3 , —NHC(O)OC(CH 3 ) 3 , —NHC(O)OCH 2 (phenyl), —NHC(O)OCH 2 (tetrahydrofuranyl), or —NHC(O)O(tetrahydropyranyl); 
 (v) —OCH 2 CH 2 NHC(O)OCH 3 , —OCH 2 CH 2 NHC(O)O(tetrahydropyranyl), —OCH 2 CH 2 NHC(O)OCH 2 (phenyl), —OCH 2 CH 2 NHC(O)O(methoxyphenyl), —OCH 2 CH 2 NHC(O)O(tetrahydrofuranyl), —OCH 2 CH 2 NHC(O)OCH 2 (tetrahydrofuranyl), —OCH 2 CH 2 NHC(O)NH(pyridinyl), —OCH 2 CH 2 N(CH 3 )C(O)NH(methylpyrimidinyl), or —OCH 2 CH(CH 3 )OC(O)OCH 2 (aminopyridinyl); 
 (vi) —OCH 2 CH 2 NHS(O) 2 CH 3  or —OCH 2 CH 2 NHS(O) 2 R w  wherein R w  is phenyl or pyridinyl, each substituted with zero to 2 substituents independently selected from F, Cl, and —CH 3 ; or 
 (vii) —OCH 2 CH 2 OC(O)NHR z , —OCH(CH 3 )CH 2 OC(O)NHR z , —OCH 2 CH(CH 3 )OC(O)NHR z , —OCH(CH 3 )CH(CH 3 )OC(O)NHR z , —OCH 2 CH(CH 2 O(isobutyl))OC(O)NHR z , —OCH 2 CH(CH 2 CH 3 )OC(O)NHR z , —OCH 2 CH(CH 2 OCH 3 )OC(O)NHR z , or —OCH 2 CH(CH 2 OCH 2 CH(CH 3 ) 2 )OC(O)NHR z  wherein R z  is H, —CH 2 CF 3 , phenyl, pyrrolyl, pyrazolyl, thiazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, oxadiazolyl, thiadiazolyl, indolyl, pyrrolo[2,3-b]pyridinyl, benzo[d]oxazolonyl, —CH 2 (pyrazolyl), —CH 2 (imidazolyl), or —CH 2 (pyridinyl), each substituted with zero to 2 substituents independently selected from F, Cl, Br, —CN, —OH, —CH 3 , —CH 2 CH 2 CH 3 , —CF 3 , —CH 2 OH, —CD 2 OH, —CH(CH 3 )OH, —CH 2 CH 2 OH, —CH 2 CH 2 CH 2 OH, —C(CH 3 ) 2 OH, —CH 2 CH(CH 3 )OH, —CH 2 C(CH 3 ) 2 OH, —CH 2 CH 2 C(O)OCH 3 , —CH 2 OP(O)(OH) 2 , —CH 2 CH 2 OP(O)(OH) 2 , —CH 2 (morpholinyl), —OCH 3 , —OCH 2 CH 2 OH, —OCH 2 CH(CH 3 )OH, —OCH 2 C(CH 3 ) 2 OH, —OCH 2 CH 2 C(CH 3 ) 2 OH, —OCH(CH 3 )CH 2 OH, —OCH 2 CH(OH)CH 2 OH, —OCH 2 CF 2 OH, —OCH 2 CF 2 CH 2 OH, —C(O)OH, —C(O)OCH 3 , —C(O)NH 2 , —C(O)NH(CH 3 ), —C(O)N(CH 3 ) 2 , —C(O)NH(CH 2 CH 2 OH), —C(O)NH(CH 2 CH(CH 3 )OH), —C(O)NH(CH 2 C(CH 3 ) 2 OH), —C(O)NH(CH 2 C(CH 3 ) 2 CH 2 OH), —C(O)NH(CH 2 CH 2 C(CH 3 ) 2 OH), —C(O)N(CH 3 )CH 2 CH 2 OH, —C(O)N(CH 3 )CH 2 C(CH 3 ) 2 OH, —C(O)NHCH 2 (hydroxymethyloxetanyl), —C(O)NH(hydroxymethylcyclobutyl), —C(O)NHCH 2 (hydroxycyclobutyl), —C(O)NHCH 2 (hydroxymethylcyclobutyl), —C(O)NHCH 2 C(CH 3 ) 2 OP(O)(OH) 2 , —C(O)(hydroxypiperidinyl), —C(O)(hydroxypyrrolidinyl), —C(O)(hydroxymethylpyrrolidinyl), —C(O)(morpholinyl), —C(O)(hydroxymethylmorpholinyl), —NH 2 , —N(CH 3 ) 2 , —NHC(O)CH 3 , —NHC(O)(chloro, fluorophenyl), —NH(CH 2 C(CH 3 ) 2 OH), —N(CH 3 )S(O) 2 CH 3 , pyrrolidinyl, morpholinyl, thiophenyl, methyl triazolyl, and oxazolidinonyl; 
 
       R 4  is H, F, or —CH 3 ; and 
       p is zero, 1, 2, or 3. 
     
     
         4 . The compound according to  claim 1  or a salt thereof, wherein:
 R 3  is: 
 
       
         
           
           
               
               
           
         
       
     
     
         5 . The compound according to  claim 1  having the structure of Formula (I): 
       
         
           
           
               
               
           
         
         or a salt thereof. 
       
     
     
         6 . The compound according to  claim 5  or a salt thereof, wherein:
 R 1  is —OCH 3 , —OCHF 2 , —OCH 2 CH 3 , or —CH 2 OCH 3 ; 
 R 2 , at each occurrence, is independently H, F, Cl, —CN, —CH 3 , —OCH 3 , or —CH 2 OH; and 
 R 3  is: 
 
       
         
           
           
               
               
           
         
       
     
     
         7 . The compound according to  claim 1  or a salt thereof, wherein said compound is selected from Examples 1-129, 131-133, 135-152, 154-176, 178-184, 186-189, 191-511, 516-624, 627-647, 658, 661-669, 671-702, 708-731, 733-738, 740-768, and 805-837. 
     
     
         8 . The compound according to  claim 1  having the structure of Formula (II): 
       
         
           
           
               
               
           
         
         or a salt thereof. 
       
     
     
         9 . The compound according to  claim 8  or a salt thereof, wherein:
 R 1  is —OH, —OCH 3 , —OCH 2 CH 3 , —OCHF 2 , —OCH 2 CHF 2 , —CH 2 OCH 3 , or —NH(CH 3 ); 
 R 2 , at each occurrence, is independently F, Cl, —CN, —CH 3 , —CH 2 OH, —CH 2 F, —CHF 2 , or —OCH 3 ; 
 R 3  is: 
 
       
         
           
           
               
               
           
         
       
       and
 R 3a , at each occurrence, is independently F, Cl, —CH 3 , —OCH 3 , —CH(OH)(trifluoromethylcyclobutyl), —OCH 2 CH(CH 3 )OC(O)NHR z , or —OCH(CH 3 )CH(CH 3 )OC(O)NHR z , wherein R z  is pyridinyl, pyrimidinyl, or benzo[d]oxazolonyl, each substituted with zero to 2 substituents independently selected from F, —OH, —CN, —CH 3 , —CF 3 , —CH 2 OH, —CH 2 CH 2 OH, —OCH 2 CH 2 OH, —OCH 3 , —CH 2 CH(CH 3 )OH, and —OCH 2 CH 2 C(CH 3 ) 2 OH. 
 
     
     
         10 . The compound according to  claim 1  or a salt thereof, wherein said compound is selected from Examples 177, 185, 190, 512-515, 625-626, 648-657, 659-660, and 769-804. 
     
     
         11 . A pharmaceutical composition, which comprises a pharmaceutically acceptable carrier and a compound according to  claim 1  or a pharmaceutically acceptable salt thereof, alone or in combination with another therapeutic agent. 
     
     
         12 . A method for the treatment of a thromboembolic disorder or the primary prophylaxis of a thromboembolic disorder, which comprises the steps of administering to a patient in need thereof a therapeutically effective amount of a compound according to  claim 1  or a pharmaceutically acceptable salt thereof, wherein the thromboembolic disorder is selected from the group consisting of arterial cardiovascular thromboembolic disorders, venous cardiovascular thromboembolic disorders, and thromboembolic disorders in the chambers of the heart or in the peripheral circulation. 
     
     
         13 . The method according to  claim 8  wherein the thromboembolic disorder is selected from the group consisting of unstable angina, an acute coronary syndrome, atrial fibrillation, myocardial infarction, transient ischemic attack, stroke, atherosclerosis, peripheral occlusive arterial disease, venous thrombosis, deep vein thrombosis, thrombophlebitis, arterial embolism, coronary arterial thrombosis, cerebral arterial thrombosis, cerebral embolism, kidney embolism, pulmonary embolism, and thrombosis resulting from medical implants, devices, and procedures in which blood is exposed to an artificial surface that promotes thrombosis. 
     
     
         14 . A method of inhibiting or preventing platelet aggregation, which comprises the step of administering to a subject in need thereof a therapeutically effective amount of a compound according to  claim 1  or a salt thereof.