JP2019532072A5 - - Google Patents
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- JP2019532072A5 JP2019532072A5 JP2019520078A JP2019520078A JP2019532072A5 JP 2019532072 A5 JP2019532072 A5 JP 2019532072A5 JP 2019520078 A JP2019520078 A JP 2019520078A JP 2019520078 A JP2019520078 A JP 2019520078A JP 2019532072 A5 JP2019532072 A5 JP 2019532072A5
- Authority
- JP
- Japan
- Prior art keywords
- phenyl
- amino
- sulfonyl
- butyl
- methyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 125000000217 alkyl group Chemical group 0.000 claims 77
- -1 substituted Chemical class 0.000 claims 60
- 125000000623 heterocyclic group Chemical group 0.000 claims 44
- 229910052739 hydrogen Inorganic materials 0.000 claims 33
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 21
- 229910052757 nitrogen Inorganic materials 0.000 claims 17
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 16
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 15
- 125000004452 carbocyclyl group Chemical group 0.000 claims 15
- 150000001875 compounds Chemical class 0.000 claims 15
- 150000003839 salts Chemical class 0.000 claims 13
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 12
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 12
- 125000003118 aryl group Chemical group 0.000 claims 10
- 229910052760 oxygen Inorganic materials 0.000 claims 10
- 125000003342 alkenyl group Chemical group 0.000 claims 9
- 229910052799 carbon Inorganic materials 0.000 claims 9
- ZEZJPIDPVXJEME-UHFFFAOYSA-N 2,4-Dihydroxypyridine Chemical compound OC=1C=CNC(=O)C=1 ZEZJPIDPVXJEME-UHFFFAOYSA-N 0.000 claims 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 5
- 206010019280 Heart failures Diseases 0.000 claims 4
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- ZSKWYFOMPUKTPB-UHFFFAOYSA-N 6-butyl-3-[4-(2-fluoro-3-methylpyridin-4-yl)phenyl]sulfonyl-4-hydroxy-5-(2-methyl-3,4-dihydro-2H-quinolin-1-yl)-1H-pyridin-2-one Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C(=NC=C1)F)C)O)N1C(CCC2=CC=CC=C12)C ZSKWYFOMPUKTPB-UHFFFAOYSA-N 0.000 claims 3
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 3
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 3
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 3
- 125000006706 (C3-C6) carbocyclyl group Chemical group 0.000 claims 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 2
- 208000024172 Cardiovascular disease Diseases 0.000 claims 2
- UQFQONCQIQEYPJ-UHFFFAOYSA-N N-methylpyrazole Chemical compound CN1C=CC=N1 UQFQONCQIQEYPJ-UHFFFAOYSA-N 0.000 claims 2
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 claims 2
- 230000002107 myocardial effect Effects 0.000 claims 2
- 208000010125 myocardial infarction Diseases 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- 238000007634 remodeling Methods 0.000 claims 2
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 2
- RLEUYGUGQVWAFP-UHFFFAOYSA-N 2-[4-[[4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-5-(N-propan-2-ylanilino)-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound CC(C)N(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(=O)N(C)C)C1=NN(C)C=C1 RLEUYGUGQVWAFP-UHFFFAOYSA-N 0.000 claims 1
- XKGZZQUMEPEDEH-UHFFFAOYSA-N 2-[4-[[4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-5-(N-propan-2-ylanilino)-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound CNC(=O)C1=CC=CC=C1C1=CC=C(C=C1)S(=O)(=O)C1=C(O)C(N(C(C)C)C2=CC=CC=C2)=C(N=C1O)C1=NN(C)C=C1 XKGZZQUMEPEDEH-UHFFFAOYSA-N 0.000 claims 1
- ODISBELNUIDXQT-UHFFFAOYSA-N 2-[4-[[4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-5-(N-propan-2-ylanilino)-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound CC(C)N(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(N)=O)C1=NN(C)C=C1 ODISBELNUIDXQT-UHFFFAOYSA-N 0.000 claims 1
- CRRLUBJBQDMDBJ-UHFFFAOYSA-N 2-[4-[[5-(3-cyano-N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-6-fluorobenzamide Chemical compound CCN(C1=CC(=CC=C1)C#N)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC(F)=C1C(N)=O)C1=NN(C)C=C1 CRRLUBJBQDMDBJ-UHFFFAOYSA-N 0.000 claims 1
- NQGBKHFOBJTAQD-UHFFFAOYSA-N 2-[4-[[5-(3-cyano-N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(#N)C=1C=C(C=CC=1)N(C=1C(=C(C(=NC=1C1=NN(C=C1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)CC NQGBKHFOBJTAQD-UHFFFAOYSA-N 0.000 claims 1
- QPBMDUANAHALKX-UHFFFAOYSA-N 2-[4-[[5-(3-cyano-N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-cyclopropylbenzamide Chemical compound CCN(c1cccc(c1)C#N)c1c(O)c(c(=O)[nH]c1-c1ccn(C)n1)S(=O)(=O)c1ccc(cc1)-c1ccccc1C(=O)NC1CC1 QPBMDUANAHALKX-UHFFFAOYSA-N 0.000 claims 1
- UXHXONFDNBFQQD-UHFFFAOYSA-N 2-[4-[[5-(3-cyano-N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound CCN(C1=CC(=CC=C1)C#N)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(=O)NC)C1=NN(C)C=C1 UXHXONFDNBFQQD-UHFFFAOYSA-N 0.000 claims 1
- LIPAJYZUOJSMDY-UHFFFAOYSA-N 2-[4-[[5-(3-cyano-N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound CCN(C1=CC(=CC=C1)C#N)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(N)=O)C1=NN(C)C=C1 LIPAJYZUOJSMDY-UHFFFAOYSA-N 0.000 claims 1
- FFDMMICIFYQYBU-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=NN(C=C1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)C1=CC=CC=C1 FFDMMICIFYQYBU-UHFFFAOYSA-N 0.000 claims 1
- XCZMFKPXPCLTPQ-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=NN(C=C1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)C1=CC=CC=C1 XCZMFKPXPCLTPQ-UHFFFAOYSA-N 0.000 claims 1
- VHXLLUHVDUHICZ-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=NN(C=C1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N)O)C1=CC=CC=C1 VHXLLUHVDUHICZ-UHFFFAOYSA-N 0.000 claims 1
- YIQCVBVOWUOLQF-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-4-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-5-fluorobenzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=NN(C=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC(=CC=1)F)C(=O)N)O)C1=CC=CC=C1 YIQCVBVOWUOLQF-UHFFFAOYSA-N 0.000 claims 1
- SZTCZIQHKLTMLT-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-4-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=NN(C=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)C1=CC=CC=C1 SZTCZIQHKLTMLT-UHFFFAOYSA-N 0.000 claims 1
- MOEKOYTYQHLRNN-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-4-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=NN(C=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)C1=CC=CC=C1 MOEKOYTYQHLRNN-UHFFFAOYSA-N 0.000 claims 1
- VTFKKKPKHBFMQA-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(2-methyl-1,3-thiazol-5-yl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound CCN(c1ccccc1)c1c(O)c(c(=O)[nH]c1-c1cnc(C)s1)S(=O)(=O)c1ccc(cc1)-c1ccccc1C(=O)NC VTFKKKPKHBFMQA-UHFFFAOYSA-N 0.000 claims 1
- KBMYMGSCAZTBKY-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(3-methylphenyl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound CCN(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=CC=C1)C(=O)N(C)C)C1=CC(C)=CC=C1 KBMYMGSCAZTBKY-UHFFFAOYSA-N 0.000 claims 1
- MJIDCFXIZIDVJL-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(3-methylphenyl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=C(C=CC=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)C1=CC=CC=C1 MJIDCFXIZIDVJL-UHFFFAOYSA-N 0.000 claims 1
- FYJQPTIHWBPCAL-UHFFFAOYSA-N 2-[4-[[5-(N-ethylanilino)-4-hydroxy-6-(3-methylphenyl)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound CCN(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=CC=C1)C(N)=O)C1=CC(C)=CC=C1 FYJQPTIHWBPCAL-UHFFFAOYSA-N 0.000 claims 1
- JCCPRKLFMMYHIP-UHFFFAOYSA-N 2-[4-[[6-(cyclopropylmethyl)-5-(N-ethylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C1(CC1)CC1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)N(C1=CC=CC=C1)CC JCCPRKLFMMYHIP-UHFFFAOYSA-N 0.000 claims 1
- AUZAWBFZVJODDF-UHFFFAOYSA-N 2-[4-[[6-(cyclopropylmethyl)-5-(N-ethylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C1(CC1)CC1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)N(C1=CC=CC=C1)CC AUZAWBFZVJODDF-UHFFFAOYSA-N 0.000 claims 1
- IXLJJDCMHBRNAF-UHFFFAOYSA-N 2-[4-[[6-(cyclopropylmethyl)-5-(N-ethylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound C1(CC1)CC1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N)O)N(C1=CC=CC=C1)CC IXLJJDCMHBRNAF-UHFFFAOYSA-N 0.000 claims 1
- UHCQQFYXVXLSFY-UHFFFAOYSA-N 2-[4-[[6-butyl-4-hydroxy-2-oxo-5-(2,3,4,5-tetrahydro-1-benzazepin-1-yl)-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)N1C2=C(CCCC1)C=CC=C2 UHCQQFYXVXLSFY-UHFFFAOYSA-N 0.000 claims 1
- HWROKMVUZLZTHD-UHFFFAOYSA-N 2-[4-[[6-butyl-4-hydroxy-2-oxo-5-(2,3,4,5-tetrahydro-1-benzazepin-1-yl)-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)N1C2=C(CCCC1)C=CC=C2 HWROKMVUZLZTHD-UHFFFAOYSA-N 0.000 claims 1
- HOZAIUOEXIYAEZ-UHFFFAOYSA-N 2-[4-[[6-butyl-4-hydroxy-5-(N-methylanilino)-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound CCCCC1=C(N(C)C2=CC=CC=C2)C(O)=C(C(O)=N1)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=CC=C1)C(N)=O HOZAIUOEXIYAEZ-UHFFFAOYSA-N 0.000 claims 1
- LXNKKNSQUHCUKU-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(2-fluoro-N-methylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound CCCCC1=C(N(C)C2=C(F)C=CC=C2)C(O)=C(C(O)=N1)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(=O)N(C)C LXNKKNSQUHCUKU-UHFFFAOYSA-N 0.000 claims 1
- TXTLEBXRQFNUSN-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(2-fluoro-N-methylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound CCCCc1[nH]c(=O)c(c(O)c1N(C)c1ccccc1F)S(=O)(=O)c1ccc(cc1)-c1ccccc1C(=O)NC TXTLEBXRQFNUSN-UHFFFAOYSA-N 0.000 claims 1
- VOLVFWRKOPUCER-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3,4-dihydro-2H-1,5-benzoxazepin-5-yl)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)N1C2=C(OCCC1)C=CC=C2 VOLVFWRKOPUCER-UHFFFAOYSA-N 0.000 claims 1
- QQTXCKKLBQCSJB-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3,4-dihydro-2H-1,5-benzoxazepin-5-yl)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)N1C2=C(OCCC1)C=CC=C2 QQTXCKKLBQCSJB-UHFFFAOYSA-N 0.000 claims 1
- HVVQKIFKUCMPNA-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3,4-dihydro-2H-1,5-benzoxazepin-5-yl)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound CCCCC1=C(N2CCCOC3=C2C=CC=C3)C(O)=C(C(O)=N1)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(N)=O HVVQKIFKUCMPNA-UHFFFAOYSA-N 0.000 claims 1
- ULTAUJUKMVDSRV-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3,4-dihydro-2H-quinolin-1-yl)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)N1CCCC2=CC=CC=C12 ULTAUJUKMVDSRV-UHFFFAOYSA-N 0.000 claims 1
- TYBNEHXUNQTDAG-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3,4-dihydro-2H-quinolin-1-yl)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)N1CCCC2=CC=CC=C12 TYBNEHXUNQTDAG-UHFFFAOYSA-N 0.000 claims 1
- AOGVFHHHSRSBQD-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3,4-dihydro-2H-quinolin-1-yl)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N)O)N1CCCC2=CC=CC=C12 AOGVFHHHSRSBQD-UHFFFAOYSA-N 0.000 claims 1
- YFOJKLBIPIPAOP-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3-cyano-N-ethylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound CCCCC1=C(N(CC)C2=CC(=CC=C2)C#N)C(O)=C(C(O)=N1)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(=O)N(C)C YFOJKLBIPIPAOP-UHFFFAOYSA-N 0.000 claims 1
- OSXWSCDGFLXMLX-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3-cyano-N-ethylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound CCCCC1=C(N(CC)C2=CC(=CC=C2)C#N)C(O)=C(C(O)=N1)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(=O)NC OSXWSCDGFLXMLX-UHFFFAOYSA-N 0.000 claims 1
- PIPIWMWCTPAIKT-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3-cyano-N-ethylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]benzamide Chemical compound CCCCC1=C(N(CC)C2=CC(=CC=C2)C#N)C(O)=C(C(O)=N1)S(=O)(=O)C1=CC=C(C=C1)C1=CC=CC=C1C(N)=O PIPIWMWCTPAIKT-UHFFFAOYSA-N 0.000 claims 1
- MOINQIBTAWXSRX-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3-cyano-N-methylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N,N-dimethylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)N(C)C)O)N(C)C1=CC(=CC=C1)C#N MOINQIBTAWXSRX-UHFFFAOYSA-N 0.000 claims 1
- KVVFMWZKVMPSBM-UHFFFAOYSA-N 2-[4-[[6-butyl-5-(3-cyano-N-methylanilino)-4-hydroxy-2-oxo-1H-pyridin-3-yl]sulfonyl]phenyl]-N-methylbenzamide Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=CC=CC=1)C(=O)NC)O)N(C)C1=CC(=CC=C1)C#N KVVFMWZKVMPSBM-UHFFFAOYSA-N 0.000 claims 1
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- URLGCVZPMZKELH-UHFFFAOYSA-N 4-hydroxy-6-(1-methylpyrazol-3-yl)-3-[4-(2-methylpyridin-3-yl)phenyl]sulfonyl-5-(N-propan-2-ylanilino)-1H-pyridin-2-one Chemical compound CC(C)N(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C)N=CC=C1)C1=NN(C)C=C1 URLGCVZPMZKELH-UHFFFAOYSA-N 0.000 claims 1
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- RSSPAHUNJMZCIU-UHFFFAOYSA-N 5-(N-ethylanilino)-3-[4-(2-fluoro-3-methylpyridin-4-yl)phenyl]sulfonyl-4-hydroxy-6-(2-methyl-1,3-thiazol-5-yl)-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=CN=C(S1)C)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C(=NC=C1)F)C)O)C1=CC=CC=C1 RSSPAHUNJMZCIU-UHFFFAOYSA-N 0.000 claims 1
- RBIVDSATZSLTQB-UHFFFAOYSA-N 5-(N-ethylanilino)-3-[4-(2-fluoro-3-methylpyridin-4-yl)phenyl]sulfonyl-4-hydroxy-6-(3-methylphenyl)-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=C(C=CC=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C(=NC=C1)F)C)O)C1=CC=CC=C1 RBIVDSATZSLTQB-UHFFFAOYSA-N 0.000 claims 1
- WSZQWZHRNAPOQM-UHFFFAOYSA-N 5-(N-ethylanilino)-3-[4-(6-fluoro-2-methylpyridin-3-yl)phenyl]sulfonyl-4-hydroxy-6-(1-methylpyrazol-3-yl)-1H-pyridin-2-one Chemical compound CCN(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=CC=C(F)N=C1C)C1=NN(C)C=C1 WSZQWZHRNAPOQM-UHFFFAOYSA-N 0.000 claims 1
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- CRZRPZWKYVYUSK-UHFFFAOYSA-N 5-(N-ethylanilino)-3-[4-(6-fluoro-2-methylpyridin-3-yl)phenyl]sulfonyl-4-hydroxy-6-(2-methyl-1,3-thiazol-5-yl)-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=CN=C(S1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=NC(=CC=1)F)C)O)C1=CC=CC=C1 CRZRPZWKYVYUSK-UHFFFAOYSA-N 0.000 claims 1
- WXAVJFFEWOSSAO-UHFFFAOYSA-N 5-(N-ethylanilino)-3-[4-(6-fluoro-2-methylpyridin-3-yl)phenyl]sulfonyl-4-hydroxy-6-(3-methylphenyl)-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=C(C=CC=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=NC(=CC=1)F)C)O)C1=CC=CC=C1 WXAVJFFEWOSSAO-UHFFFAOYSA-N 0.000 claims 1
- DKAJTRPMRINCRA-UHFFFAOYSA-N 5-(N-ethylanilino)-4-hydroxy-3-[4-(3-methylpyridin-4-yl)phenyl]sulfonyl-6-(2-methyl-1,3-thiazol-5-yl)-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=CN=C(S1)C)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=NC=C1)C)O)C1=CC=CC=C1 DKAJTRPMRINCRA-UHFFFAOYSA-N 0.000 claims 1
- XWKLQBVJYOJXJJ-UHFFFAOYSA-N 5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-3-[4-(2-methylpyridin-3-yl)phenyl]sulfonyl-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=NN(C=C1)C)O)S(=O)(=O)C1=CC=C(C=C1)C=1C(=NC=CC=1)C)O)C1=CC=CC=C1 XWKLQBVJYOJXJJ-UHFFFAOYSA-N 0.000 claims 1
- BFRGUCAOFPBPPH-UHFFFAOYSA-N 5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-3-yl)-3-[4-(3-methylpyridin-4-yl)phenyl]sulfonyl-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C1=NN(C=C1)C)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=NC=C1)C)O)C1=CC=CC=C1 BFRGUCAOFPBPPH-UHFFFAOYSA-N 0.000 claims 1
- XYKXTEPDZYLNTC-UHFFFAOYSA-N 5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-4-yl)-3-[4-(2-methylpyridin-3-yl)phenyl]sulfonyl-1H-pyridin-2-one Chemical compound CCN(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C)N=CC=C1)C1=CN(C)N=C1 XYKXTEPDZYLNTC-UHFFFAOYSA-N 0.000 claims 1
- MIGZPFHOCCENRB-UHFFFAOYSA-N 5-(N-ethylanilino)-4-hydroxy-6-(1-methylpyrazol-4-yl)-3-[4-(3-methylpyridin-4-yl)phenyl]sulfonyl-1H-pyridin-2-one Chemical compound CCN(C1=CC=CC=C1)C1=C(N=C(O)C(=C1O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C)C=NC=C1)C1=CN(C)N=C1 MIGZPFHOCCENRB-UHFFFAOYSA-N 0.000 claims 1
- FTWOTIXPFDOORI-UHFFFAOYSA-N 5-(N-ethylanilino)-4-hydroxy-6-(3-methylphenyl)-3-[4-(3-methylpyridin-4-yl)phenyl]sulfonyl-1H-pyridin-2-one Chemical compound C(C)N(C=1C(=C(C(=NC=1C=1C=C(C=CC=1)C)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=NC=C1)C)O)C1=CC=CC=C1 FTWOTIXPFDOORI-UHFFFAOYSA-N 0.000 claims 1
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- CGTCNDKPBWXKII-UHFFFAOYSA-N 6-butyl-5-(3,4-dihydro-2H-quinolin-1-yl)-4-hydroxy-3-[4-(3-methylpyridin-4-yl)phenyl]sulfonyl-1H-pyridin-2-one Chemical compound C(CCC)C1=C(C(=C(C(=N1)O)S(=O)(=O)C1=CC=C(C=C1)C1=C(C=NC=C1)C)O)N1CCCC2=CC=CC=C12 CGTCNDKPBWXKII-UHFFFAOYSA-N 0.000 claims 1
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| BR112018012112A2 (pt) | 2015-12-16 | 2018-12-04 | Bristol-Myers Squibb Company | heteroaril-hidroxipirimidinonas como agonistas do receptor apj |
| CN109641843B (zh) * | 2016-06-14 | 2022-07-19 | 百时美施贵宝公司 | 作为apj激动剂的4-羟基-3-磺酰基吡啶-2(1h)-酮 |
| WO2017218633A1 (en) | 2016-06-14 | 2017-12-21 | Bristol-Myers Squibb Company | 6-hydroxy-5-(phenyl/heteroarylsulfonyl)pyrimidin-4(1h)-one as apj agonists |
| WO2018097944A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Triazole furan compounds as agonists of the apj receptor |
| WO2018097945A1 (en) | 2016-11-16 | 2018-05-31 | Amgen Inc. | Heteroaryl-substituted triazoles as apj receptor agonists |
| EP3541804B1 (en) | 2016-11-16 | 2025-01-22 | Amgen Inc. | Cycloalkyl substituted triazole compounds as agonists of the apj receptor |
| EP3541803B1 (en) | 2016-11-16 | 2020-12-23 | Amgen Inc. | Triazole pyridyl compounds as agonists of the apj receptor |
| MA46824A (fr) | 2016-11-16 | 2019-09-25 | Amgen Inc | Composés de triazole substitués par alkyle en tant qu'agonistes du récepteur apj |
| US10906890B2 (en) | 2016-11-16 | 2021-02-02 | Amgen Inc. | Triazole phenyl compounds as agonists of the APJ receptor |
| MA50509A (fr) | 2017-11-03 | 2021-06-02 | Amgen Inc | Agonistes de triazole fusionnés du récepteur apj |
| MA52487A (fr) | 2018-05-01 | 2021-03-10 | Amgen Inc | Pyrimidinones substituées en tant qu'agonistes du récepteur apj |
Family Cites Families (9)
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|---|---|---|---|---|
| RU2009106214A (ru) * | 2006-07-26 | 2010-09-10 | Новартис АГ (CH) | Ингибиторы ундекапренилпирофосфатсинтазы |
| US10377718B2 (en) | 2014-06-06 | 2019-08-13 | Research Triangle Institute | Apelin receptor (APJ) agonists and uses thereof |
| PE20180506A1 (es) * | 2015-06-03 | 2018-03-09 | Bristol Myers Squibb Co | Agonistas de receptor de apelina (apj) de 4-hidroxi-3-(heteroaril) piridin-2-ona como para uso en el tratamiento de trastornos cardiovasculares |
| EA034857B1 (ru) * | 2015-10-14 | 2020-03-30 | Бристол-Маерс Сквибб Компани | 2,4-дигидроксиникотинамиды как агонисты apj |
| MX381160B (es) | 2015-12-04 | 2025-03-12 | Bristol Myers Squibb Co | Agonistas del receptor de apelina y metodos de uso. |
| BR112018012112A2 (pt) | 2015-12-16 | 2018-12-04 | Bristol-Myers Squibb Company | heteroaril-hidroxipirimidinonas como agonistas do receptor apj |
| CA3018346A1 (en) | 2016-03-24 | 2017-09-28 | Bristol-Myers Squibb Company | 6-hydroxy-4-oxo-1,4-dihydropyrimidine-5-carboxamides as apj agonists |
| CN109641843B (zh) * | 2016-06-14 | 2022-07-19 | 百时美施贵宝公司 | 作为apj激动剂的4-羟基-3-磺酰基吡啶-2(1h)-酮 |
| WO2017218633A1 (en) | 2016-06-14 | 2017-12-21 | Bristol-Myers Squibb Company | 6-hydroxy-5-(phenyl/heteroarylsulfonyl)pyrimidin-4(1h)-one as apj agonists |
-
2017
- 2017-10-12 US US16/340,172 patent/US10669258B2/en active Active
- 2017-10-12 EP EP17788068.9A patent/EP3526198B1/en active Active
- 2017-10-12 JP JP2019520078A patent/JP7037558B2/ja active Active
- 2017-10-12 KR KR1020197013282A patent/KR102521956B1/ko active Active
- 2017-10-12 CN CN201780076365.4A patent/CN110072850B/zh active Active
- 2017-10-12 WO PCT/US2017/056265 patent/WO2018071622A1/en not_active Ceased
- 2017-10-12 ES ES17788068T patent/ES2820223T3/es active Active
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