US2010331306A1PendingUtilityA1

Heterocyclic compounds and their uses

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Assignee: AMGEN INCPriority: Jun 25, 2009Filed: Jun 25, 2010Published: Dec 30, 2010
Est. expiryJun 25, 2029(~3 yrs left)· nominal 20-yr term from priority
A61P 37/08A61P 7/06A61P 37/00A61P 35/00A61P 37/02A61P 37/06A61P 7/00A61P 9/12A61P 9/10A61P 43/00A61P 35/02A61P 3/10A61P 27/02A61P 25/00A61P 29/00A61P 17/00A61P 13/10A61P 19/00A61P 21/04A61P 11/00A61P 11/06A61P 19/02A61P 1/00A61P 17/06C07D 401/14C07D 471/04C07D 401/12C07D 487/04C07D 473/34A61K 31/4375A61K 31/444
43
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Claims

Abstract

Substituted bicyclic heteroaryls and compositions containing them, for the treatment of general inflammation, arthritis, rheumatic diseases, osteoarthritis, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, psoriasis, skin complaints with inflammatory components, chronic inflammatory conditions, including but not restricted to autoimmune diseases such as systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions including all forms of hypersensitivity. The present invention also enables methods for treating cancers that are mediated, dependent on or associated with p110δ activity, including but not restricted to leukemias, such as Acute Myeloid leukaemia (AML) Myelo-dysplastic syndrome (MDS) myelo-proliferative diseases (MPD) Chronic Myeloid Leukemia (CML) T-cell Acute Lymphoblastic leukaemia (T-ALL) B-cell Acute Lymphoblastic leukaemia (B-ALL) Non Hodgkins Lymphoma (NHL) B-cell lymphoma and solid tumors, such as breast cancer.

Claims

exact text as granted — not AI-modified
1 . A compound having the structure: 
       
         
           
           
               
               
           
         
       
       or any pharmaceutically-acceptable salt thereof, wherein:
 X 1  is C(R 10 ) or N; 
 X 2  is C or N; 
 X 3  is C or N; 
 X 4  is C or N; 
 X 5  is C or N; wherein at least two of X 2 , X 3 , X 4  and X 5  are C; 
 X 6  is C(R 6 ) or N; 
 X 7  is C(R 7 ) or N; 
 X 8  is C(R 10 ) or N; 
 Y is N(R 8 ), O or S; 
 n is 0, 1, 2 or 3; 
 R 1  is a direct-bonded, C 1-4 alk-linked, OC 1-2 alk-linked, C 1-2 alkO-linked, N(R a )-linked or O-linked saturated, partially-saturated or unsaturated 5-, 6- or 7-membered monocyclic or 8-, 9-, 10- or 11-membered bicyclic ring containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, but containing no more than one O or S atom, substituted by 0, 1, 2 or 3 substituents independently selected from halo, C 1-6 alk, C 1-4 haloalk, cyano, nitro, —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —OR a , —OC(═O)R a , —OC(═O)NR a R a , —OC(═O)N(R a )S(═O) 2 R a , —OC 2-6 alkNR a R a , —OC 2-6 alkOR a , —SR a , —S(═O)R a , —S(═O) 2 R a , —S(═O) 2 NR a R a , —S(═O) 2 N(R a )C(═O)R a , —S(═O) 2 N(R a )C(═O)OR a , —S(═O) 2 N(R a )C(═O)NR a R a , —NR a R a , —N(R a )C(═O)R a , —N(R a )C(═O)OR a , —N(R a )C(═O)NR a R a , —N(R a )C(═NR a )NR a R a , —N(R a )S(═O) 2 R a , —N(R a )S(═O) 2 NR a R a , —NR a C 2-6 alkNR a R a  and —NR a C 2-6 alkOR a , wherein the available carbon atoms of the ring are additionally substituted by 0, 1 or 2 oxo or thioxo groups, and wherein the ring is additionally substituted by 0 or 1 directly bonded, SO 2  linked, C(═O) linked or CH 2  linked group selected from phenyl, pyridyl, pyrimidyl, morpholino, piperazinyl, piperadinyl, cyclopentyl, cyclohexyl all of which are further substituted by 0, 1, 2 or 3 independent R b  groups; 
 R 2  is selected from H, halo, C 1-6 alk, C 1-4 haloalk, cyano, nitro, OR a , NR a R a , —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —S(═O)R a , —S(═O) 2 R a , —S(═O) 2 NR a R a , —S(═O) 2 N(R a )C(═O)R a , —S(═O) 2 N(R a )C(═O)OR a  and —S(═O) 2 N(R a )C(═O)NR a R a ; 
 R 3  is selected from H, halo, nitro, cyano, C 1-4 alk, OC 1-4 alk, OC 1-4 haloalk, NHC 1-4 alk, N(C 1-4 alk)C 1-4 alk and C 1-4 haloalk; 
 R 4  is, independently, in each instance, halo, nitro, cyano, C 1-4 alk, OC 1-4 alk, OC 1-4 haloalk, NHC 1-4 alk, N(C 1-4 alk)C 1-4 alk, C 1-4 haloalk or an unsaturated 5-, 6- or 7-membered monocyclic ring containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, but containing no more than one O or S, the ring being substituted by 0, 1, 2 or 3 substituents selected from halo, C 1-4 alk, C 1-3 haloalk, —OC 1-4 alk, —NH 2 , —NHC 1-4 alk, —N(C 1-4 alk)C 1-4 alk; 
 R 5  is, independently, in each instance, H, halo, C 1-6 alk, C 1-4 haloalk, or C 1-6 alk substituted by 1, 2 or 3 substituents selected from halo, cyano, OH, OC 1-4 alk, C 1-4 alk, C 1-3 haloalk, OC 1-4 alk, NH 2 , NHC 1-4 alk and N(C 1-4 alk)C 1-4 alk; or both R 5  groups together form a C 3-6 spiroalk substituted by 0, 1, 2 or 3 substituents selected from halo, cyano, OH, OC 1-4 alk, C 1-4 alk, C 1-3 haloalk, OC 1-4 alk, NH 2 , NHC 1-4 alk and N(C 1-4 alk)C 1-4 alk; 
 R 6  is H, halo, NHR 9  or OH, cyano, OC 1-4 alk, C 1-4 alk, C 1-3 haloalk, OC 1-4 alk, —C(═O)OR a , —C(═O)N(R a )R a  or —N(R a )C(═O)R b ; 
 R 7  is selected from H, halo, C 1-4 haloalk, cyano, nitro, —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —OR a , —OC(═O)R a , —OC(═O)NR a R a , —OC(═O)N(R a )S(═O) 2 R a , —OC 2-6 alkNR a R a , —OC 2-6 alkOR a , —SR a , —S(═O)R a , —S(═O) 2 R a , —S(═O) 2 NR a R a , —S(═O) 2 N(R a )C(═O)R a , —S(═O) 2 N(R a )C(═O)OR a , —S(═O) 2 N(R a )C(═O)NR a R a , —NR a R a , —N(R a )C(═O)R a , —N(R a )C(═O)OR a , —N(R a )C(═O)NR a R a , —N(R a )C(═NR a )NR a R a , —N(R a )S(═O) 2 R a , —N(R a )S(═O) 2 NR a R a , —NR a C 2-6 alkNR a R a , —NR a C 2-6 alkOR a  and C 1-6 alk, wherein the C 1-6 alk is substituted by 0, 1, 2 or 3 substituents selected from halo, C 1-4 haloalk, cyano, nitro, —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —OR a , —OC(═O)R a , —OC(═O)NR a R a , —OC(═O)N(R a )S(═O) 2 R a , —OC 2-6 alkNR a R a , —OC 2-6 alkOR a , —SR a , —S(═O)R a , —S(═O) 2 R a , —S(═O) 2 NR a R a , —S(═O) 2 N(R a )C(═O)R a , —S(═O) 2 N(R a )C(═O)OR a , —S(═O) 2 N(R a )C(═O)NR a R a , —NR a R a , —N(R a )C(═O)R a , —N(R a )C(═O)OR a , —N(R a )C(═O)NR a R a , —N(R a )C(═NR a )NR a R a , —N(R a )S(═O) 2 R a , —N(R a )S(═O) 2 NR a R a , —NR a C 2-6 alkNR a R a  and —NR a C 2-6 alkOR a , and the C 1-6 alk is additionally substituted by 0 or 1 saturated, partially-saturated or unsaturated 5-, 6- or 7-membered monocyclic rings containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, but containing no more than one O or S, wherein the available carbon atoms of the ring are substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2 or 3 substituents independently selected from halo, nitro, cyano, C 1-4 alk, OC 1-4 alk, OC 1-4 haloalk, NHC 1-4 alk, N(C 1-4 alk)C 1-4 alk and C 1-4 haloalk; or R 7  and R 8  together form a —C═N— bridge wherein the carbon atom is substituted by H, halo, cyano, or a saturated, partially-saturated or unsaturated 5-, 6- or 7-membered monocyclic ring containing 0, 1, 2, 3 or 4 atoms selected from N, O and S, but containing no more than one O or S, wherein the available carbon atoms of the ring are substituted by 0, 1 or 2 oxo or thioxo groups, wherein the ring is substituted by 0, 1, 2, 3 or 4 substituents selected from halo, C 1-6 alk, C 1-4 haloalk, cyano, nitro, —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —OR a , —OC(═O)R a , —OC(═O)NR a R a , —OC(═O)N(R a )S(═O) 2 R a , —OC 2-6 alkNR a R a , —OC 2-6 alkOR a , —SR a , —S(═O)R a , —S(═O) 2 R a , —S(═O) 2 NR a R a , —S(═O) 2 N(R a )C(═O)R a , —S(═O) 2 N(R a )C(═O)OR a , —S(═O) 2 N(R a )C(═O)NR a R a , —NR a R a , —N(R a )C(═O)R a , —N(R a )C(═O)OR a , —N(R a )C(═O)NR a R a , —N(R a )C(═NR a )NR a R a , —N(R a )S(═O) 2 R a , —N(R a )S(═O) 2 NR a R a , —NR a C 2-6 alkNR a R a  and —NR a C 2-6 alkOR a ; or R 7  and R 9  together form a —N═C— bridge wherein the carbon atom is substituted by H, halo, C 1-6 alk, C 1-4 haloalk, cyano, nitro, OR a , NR a R a , —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —S(═O)R a , —S(═O) 2 R a  or —S(═O) 2 NR a R a ; 
 R 8  is H, C 1-6 alk, C(═O)N(R a )R a , C(═O)R b  or C 1-4 haloalk; 
 R 9  is H, C 1-6 alk or C 1-4 haloalk; 
 R 10  is in each instance H, halo, C 1-3 alk, C 1-3 haloalk or cyano; 
 R 11  is selected from H, halo, C 1-6 alk, C 1-4 haloalk, cyano, nitro, —C(═O)R a , —C(═O)OR a , —C(═O)NR a R a , —C(═NR a )NR a R a , —OR a , —OC(═O)R a , —OC(═O)NR a R a , —OC(═O)N(R a )S(═O) 2 R a , —OC 2-6 alkNR a R a , —OC 2-6 alkOR a , —SR a , —S(═O)R a , —S(═O) 2 R b , —S(═O) 2 NR a R a , —S(═O) 2 N(R a )C(═O)R a , —S(═O) 2 N(R a )C(═O)OR a , —S(═O) 2 N(R a )C(═O)NR a R a , —NR a R a , —N(R a )C(═O)R a , —N(R a )C(═O)OR a , —N(R a )C(═O)NR a R a , —N(R a )C(═NR a )NR a R a , —N(R a )S(═O) 2 R a , —N(R a )S(═O) 2 NR a R a , —NR a C 2-6 alkNR a R a , —NR a C 2-6 alkOR a , —NR a C 2-6 alkCO 2 R a , —NR a C 2-6 alkSO 2 R b , —CH 2 C(═O)R a , —CH 2 C(═O)OR a , —CH 2 C(═O)NR a R a , —CH 2 C(═NR a )NR a R a , —CH 2 OR a , —CH 2 C(═O)R a , —CH 2 C(═O)NR a R a , —CH 2 C(═O)N(R a )S(═O) 2 R a , —CH 2 OC 2-6 alkNR a R a , —CH 2 OC 2-6 alkOR a , —CH 2 SR a , —CH 2 S(═O)R a , —CH 2 S(═O) 2 R b , —CH 2 S(═O) 2 NR a R a , —CH 2 S(═O) 2 N(R a )C(═O)R a , —CH 2 S(═O) 2 N(R a )C(═O)OR a , —CH 2 S(═O) 2 N(R a )C(═O)NR a R a , —CH 2 NR a R a , —CH 2 N(R a )C(═O)R a , —CH 2 N(R a )C(═O)OR a , —CH 2 N(R a )C(═O)NR a R a , —CH 2 N(R a )C(═NR a )NR a R a , —CH 2 N(R a )S(═O) 2 R a , —CH 2 N(R a )S(═O) 2 NR a R a , —CH 2 NR a C 2-6 alkNR a R a , —CH 2 NR a C 2-6 alkOR a , —CH 2 NR a C 2-6 alkCO 2 R a , —CH 2 NR a C 2-6 alkSO 2 R b , —CH 2 R c , —C(═O)R c  and —C(═O)N(R a )R c ; 
 R a  is independently, at each instance, H or R b ; 
 R b  is independently, at each instance, phenyl, benzyl or C 1-6 alk, the phenyl, benzyl and C 1-6 alk being substituted by 0, 1, 2 or 3 substituents selected from halo, C 1-4 alk, C 1-3 haloalk, —OH, —OC 1-4 alk, —NH 2 , —NHC 1-4 alk and —N(C 1-4 alk)C 1-4 alk; and 
 R c  is a saturated or partially-saturated 4-, 5- or 6-membered ring containing 1, 2 or 3 heteroatoms selected from N, O and S, the ring being substituted by 0, 1, 2 or 3 substituents selected from halo, C 1-4 alk, C 1-3 haloalk, —OC 1-4 alk, —NH 2 , —NHC 1-4 alk and —N(C 1-4 alk)C 1-4 alk. 
 
     
     
         2 . A compound according to  claim 1 , wherein the compound is:
 4-amino-1-((1S)-1-(6-fluoro-3-(5-fluoro-3-pyridinyl)-2-quinolinyl)ethyl)-1H-pyrazolo[3,4-d]pyrimidine-3-carbonitrile;   4-amino-1-((1R)-1-(6-fluoro-3-(5-fluoro-3-pyridinyl)-2-quinolinyl)ethyl)-1H-pyrazolo[3,4-d]pyrimidine-3-carbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-3-(6-(methylsulfonyl)-2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   N-(1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-9H-purin-6-amine;   N-((1S)-1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-9H-purin-6-amine;   N-((1R)-1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-9H-purin-6-amine;   N-(1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-4-pyrimidinamine;   N-(1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-4,6-pyrimidinediamine;   N˜4˜-((1R)-1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-2,4-pyrimidinediamine;   4-amino-6-((1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-((1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-6-hydroxy-5-pyrimidinecarbonitrile;   4-amino-1-((1S)-1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-1H-pyrazolo[3,4-d]pyrimidine-3-carbonitrile;   4-amino-1-((1R)-1-(6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)-1H-pyrazolo[3,4-d]pyrimidine-3-carbonitrile;   4-amino-6-((1-(5-chloro-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(5-chloro-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1R)-1-(5-chloro-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-3-(2-pyridinyl)-5-quinolinecarbonitrile;   2-((1R)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-3-(2-pyridinyl)-5-quinolinecarbonitrile;   4-amino-6-((1-(3-(2-pyridinyl)-1,8-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((1-(3-(2-pyridinyl)-1,6-naphthyridin-2-yl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((1-(6-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((1-(6-fluoro-4-(methylsulfanyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((8-fluoro-3-(2-(methylsulfonyl)phenyl)-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((8-fluoro-3-(2-pyridinyl)-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((8-fluoro-3-phenyl-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((5-fluoro-3-phenyl-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((5-fluoro-3-(3-fluorophenyl)-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((3-(3,5-difluorophenyl)-5-fluoro-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((5-fluoro-3-(2-(methylsulfonyl)phenyl)-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((5-fluoro-3-(2-pyridinyl)-2-quinolinyl)methyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(4-(dimethylamino)-6-fluoro-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-(4-morpholinyl)-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-(3-hydroxy-1-azetidinyl)-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N,N-dimethyl-3-phenyl-4-quinolinecarboxamide;   4-amino-6-(((1S)-1-(6-fluoro-4-(4-morpholinylcarbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-4-(((3S)-3-hydroxy-1-pyrrolidinyl)carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(4-((1,1-dioxido-4-thiomorpholinyl)-carbonyl)-6-fluoro-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-phenyl-4-quinolinecarbonitrile;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-phenyl-4-quinolinecarbonitrile;   2-((1R)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-phenyl-4-quinolinecarbonitrile;   methyl 2-(-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-phenyl-4-quinolinecarboxylate;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-phenyl-4-quinolinecarboxylic acid;   2-((1S)-1-((6-amino-5-carbamoyl-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-phenyl-4-quinolinecarboxylic acid;   2-(-1-(6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-methyl-3-phenyl-4-quinolinecarboxamide;   4-amino-6-((-1-(6-fluoro-3-phenyl-4-(1-piperazinylcarbonyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-((4-methyl-1-piperazinyl)carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-(-1-(6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N,N-dimethyl-3-phenyl-4-quinolinecarboxamide;   4-amino-6-((-1-(6-fluoro-4-(((3R)-3-hydroxy-1-pyrrolidinyl)carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((1-(6-fluoro-3-phenyl-4-(1-pyrrolidinylcarbonyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-(4-morpholinylcarbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-(((3S)-3-hydroxy-1-pyrrolidinyl)carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-(((3R)-3-hydroxy-1-pyrrolidinyl)-carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidine-carbonitrile;   4-amino-6-((1-(4-((1,1-dioxido-4-thiomorpholinyl)carbonyl)-6-fluoro-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidine-carbonitrile;   4-amino-6-((1-(6-fluoro-4-((3-hydroxy-1-azetidinyl)carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((1-(6-fluoro-4-((3-methoxy-1-azetidinyl)carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-(1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-(2-(4-morpholinyl)ethyl)-3-phenyl-4-quinolinecarboxamide;   4-amino-6-((-1-(6-fluoro-4-(hydroxymethyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-3-phenyl-4-(1-piperazinylcarbonyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-((1S)-1-(6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-methyl-3-phenyl-4-quinolinecarboxamide;   4-amino-6-((-1-(6-fluoro-4-((methylsulfonyl)methyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-4-((3-hydroxy-1-azetidinyl)-carbonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidine-carbonitrile;   4-amino-6-(((1S)-1-(4-((1,1-dioxido-4-thiomorpholinyl)carbonyl)-6-fluoro-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N,N-dimethyl-3-phenyl-4-quinolinecarboxamide;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N,N-dimethyl-3-phenyl-4-quinolinecarboxamide;   4-amino-6-((-1-(6-fluoro-4-(4-morpholinylmethyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-((1S)-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-N-ethyl-6-fluoro-3-phenyl-4-quinolinecarboxamide;   2-(-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-(1-methylethyl)-3-phenyl-4-quinolinecarboxamide;   2-(-1-((6-amino-5-cyano-4-pyrimidinyl)amino)ethyl)-N-(cyclopropylmethyl)-6-fluoro-3-phenyl-4-quinolinecarboxamide;   4-amino-6-(((1S)-1-(6-fluoro-4-methoxy-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1R)-1-(6-fluoro-4-methoxy-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(3-(3,5-difluorophenyl)-6-fluoro-4-methoxy-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(-1-(6-fluoro-4-((2-methoxyethyl)amino)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(-1-(4-((2-(dimethylamino)ethyl)amino)-6-fluoro-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-4-((2-methoxyethyl)amino)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1R)-1-(6-fluoro-4-((2-methoxyethyl)amino)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(-1-(6-fluoro-4-((2-(methylsulfonyl)ethyl)amino)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(-1-(6-fluoro-4-((2-hydroxyethyl)amino)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-4-((2-(methylsulfonyl)ethyl)amino)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(6-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   N-(1-(6-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)ethyl)-9H-purin-6-amine;   N-(-1-(5-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)ethyl)-9H-purin-6-amine;   4-amino-6-((-1-(6-fluoro-4-((R)-(2-hydroxyethyl)sulfinyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1R)-1-(5-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-(((1S)-1-(5-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   N-((1S)-1-(6-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)-ethyl)-9H-purin-6-amine;   N-((1R)-1-(6-fluoro-4-(methylsulfonyl)-3-phenyl-2-quinolinyl)-ethyl)-9H-purin-6-amine;   4-amino-6-((-1-(3-(3,5-difluorophenyl)-6-fluoro-4-(methyl-sulfonyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   4-amino-6-((-1-(6-fluoro-4-((S)-(2-hydroxyethyl)sulfinyl)-3-phenyl-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile;   2-(1-(6-Amino-5-cyanopyrimidin-4-ylamino)ethyl)-6-fluoro-N-methyl-3-(pyridin-2-yl)quinoline-4-carboxamide;   (S)-2-(1-(6-Amino-5-cyanopyrimidin-4-ylamino)ethyl)-N-ethyl-6-fluoro-3-(pyridin-2-yl)quinoline-4-carboximidamide;   (S)-2-(1-(6-Amino-5-cyanopyrimidin-4-ylamino)ethyl)-6-fluoro-N-(2-hydroxyethyl)-3-(pyridin-2-yl)quinoline-4-carboxamide;   (S)-2-(1-(6-Amino-5-cyanopyrimidin-4-ylamino)ethyl)-N-cyclopropyl-6-fluoro-3-(pyridin-2-yl)quinoline-4-carboxamide;   2-1-(((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-3-(2-pyridinyl)-4-quinolinecarboxylic acid;   2-(-1-(((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-methyl-3-(2-pyridinyl)-4-quinolinecarboxamide;   2-((1R)-1-((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N-methyl-3-(2-pyridinyl)-4-quinolinecarboxamide;   2-(1-((6-Amino-5-cyano-4-pyrimidinyl)amino)ethyl)-6-fluoro-N,N-dimethyl-3-(2-pyridinyl)-4-quinolinecarboxamide;   4-Amino-6-((1-(6-fluoro-4-(1-piperazinylcarbonyl)-3-(2-pyridinyl)-2-quinolinyl)ethyl)amino)-5-pyrimidinecarbonitrile; or   4-amino-6-(1-(6-fluoro-4-(3-hydroxyazetidine-1-carbonyl)-3-(pyridin-2-yl)quinolin-2-yl)ethylamino)pyrimidine-5-carbonitrile; or any pharmaceutically-acceptable salt thereof.   
     
     
         3 . A method of treating rheumatoid arthritis, ankylosing spondylitis, osteoarthritis, psoriatic arthritis, psoriasis, inflammatory diseases and autoimmune diseases, inflammatory bowel disorders, inflammatory eye disorders, inflammatory or unstable bladder disorders, skin complaints with inflammatory components, chronic inflammatory conditions, autoimmune diseases, systemic lupus erythematosis (SLE), myestenia gravis, rheumatoid arthritis, acute disseminated encephalomyelitis, idiopathic thrombocytopenic purpura, multiples sclerosis, Sjoegren's syndrome and autoimmune hemolytic anemia, allergic conditions and hypersensitivity, comprising the step of administering a compound according to  claim 1 . 
     
     
         4 . A method of treating cancers, which are mediated, dependent on or associated with p110δ activity, comprising the step of administering a compound according to  claim 1 . 
     
     
         5 . A pharmaceutical composition comprising a compound according to  claim 1  and a pharmaceutically-acceptable diluent or carrier.

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