CA2855346A1 - Thieno- and furo - pyrimidines and pyridines, useful as potassium channel inhibitors - Google Patents
Thieno- and furo - pyrimidines and pyridines, useful as potassium channel inhibitors Download PDFInfo
- Publication number
- CA2855346A1 CA2855346A1 CA2855346A CA2855346A CA2855346A1 CA 2855346 A1 CA2855346 A1 CA 2855346A1 CA 2855346 A CA2855346 A CA 2855346A CA 2855346 A CA2855346 A CA 2855346A CA 2855346 A1 CA2855346 A1 CA 2855346A1
- Authority
- CA
- Canada
- Prior art keywords
- optionally substituted
- thieno
- pyrimidin
- alkyl
- phenyl
- 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.)
- Abandoned
Links
- 239000003112 inhibitor Substances 0.000 title abstract description 23
- 102000004257 Potassium Channel Human genes 0.000 title abstract description 10
- 108020001213 potassium channel Proteins 0.000 title abstract description 10
- 150000003222 pyridines Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract description 327
- 238000011282 treatment Methods 0.000 claims abstract description 78
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 39
- 230000005764 inhibitory process Effects 0.000 claims abstract description 31
- 201000010099 disease Diseases 0.000 claims abstract description 29
- 230000001404 mediated effect Effects 0.000 claims abstract description 24
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 13
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 11
- 238000002560 therapeutic procedure Methods 0.000 claims abstract description 10
- -1 ̈CN Chemical group 0.000 claims description 204
- 238000000034 method Methods 0.000 claims description 138
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 125
- 125000000217 alkyl group Chemical group 0.000 claims description 122
- 239000000203 mixture Substances 0.000 claims description 91
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 86
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 63
- 125000001072 heteroaryl group Chemical group 0.000 claims description 62
- 206010003658 Atrial Fibrillation Diseases 0.000 claims description 60
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 56
- 125000003386 piperidinyl group Chemical group 0.000 claims description 53
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 51
- 239000003814 drug Substances 0.000 claims description 48
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 44
- 125000003107 substituted aryl group Chemical group 0.000 claims description 42
- 229910052757 nitrogen Inorganic materials 0.000 claims description 38
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 36
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 34
- 125000002757 morpholinyl group Chemical group 0.000 claims description 33
- 125000003118 aryl group Chemical group 0.000 claims description 26
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 26
- 230000001746 atrial effect Effects 0.000 claims description 25
- 125000001424 substituent group Chemical group 0.000 claims description 25
- 230000004064 dysfunction Effects 0.000 claims description 20
- 230000002265 prevention Effects 0.000 claims description 20
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 19
- 206010003662 Atrial flutter Diseases 0.000 claims description 18
- 229910052717 sulfur Inorganic materials 0.000 claims description 18
- 229910006074 SO2NH2 Inorganic materials 0.000 claims description 16
- 208000001435 Thromboembolism Diseases 0.000 claims description 15
- 210000001013 sinoatrial node Anatomy 0.000 claims description 15
- 206010003119 arrhythmia Diseases 0.000 claims description 14
- 125000003106 haloaryl group Chemical group 0.000 claims description 14
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 14
- 125000004953 trihalomethyl group Chemical group 0.000 claims description 14
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 13
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 13
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 claims description 13
- 125000005968 oxazolinyl group Chemical group 0.000 claims description 13
- 230000006793 arrhythmia Effects 0.000 claims description 12
- 125000002393 azetidinyl group Chemical group 0.000 claims description 12
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 12
- 125000006004 trihaloethyl group Chemical group 0.000 claims description 12
- 125000004366 heterocycloalkenyl group Chemical group 0.000 claims description 11
- 125000006008 trihaloethoxy group Chemical group 0.000 claims description 11
- 125000004951 trihalomethoxy group Chemical group 0.000 claims description 11
- 208000005189 Embolism Diseases 0.000 claims description 9
- 208000006011 Stroke Diseases 0.000 claims description 9
- 125000003725 azepanyl group Chemical group 0.000 claims description 9
- 230000000747 cardiac effect Effects 0.000 claims description 9
- 208000035475 disorder Diseases 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 206010028980 Neoplasm Diseases 0.000 claims description 8
- 208000002193 Pain Diseases 0.000 claims description 8
- 206010040639 Sick sinus syndrome Diseases 0.000 claims description 8
- 208000007536 Thrombosis Diseases 0.000 claims description 8
- 201000011510 cancer Diseases 0.000 claims description 8
- 206010015037 epilepsy Diseases 0.000 claims description 8
- 230000036407 pain Effects 0.000 claims description 8
- 230000033764 rhythmic process Effects 0.000 claims description 8
- 206010006187 Breast cancer Diseases 0.000 claims description 7
- 208000026310 Breast neoplasm Diseases 0.000 claims description 7
- 208000024172 Cardiovascular disease Diseases 0.000 claims description 7
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000007634 remodeling Methods 0.000 claims description 7
- 230000028327 secretion Effects 0.000 claims description 7
- 125000005017 substituted alkenyl group Chemical group 0.000 claims description 7
- 208000019901 Anxiety disease Diseases 0.000 claims description 6
- 206010003671 Atrioventricular Block Diseases 0.000 claims description 6
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 6
- 208000018262 Peripheral vascular disease Diseases 0.000 claims description 6
- 102000006877 Pituitary Hormones Human genes 0.000 claims description 6
- 108010047386 Pituitary Hormones Proteins 0.000 claims description 6
- 230000036506 anxiety Effects 0.000 claims description 6
- 210000001992 atrioventricular node Anatomy 0.000 claims description 6
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 6
- 238000013194 cardioversion Methods 0.000 claims description 6
- 206010012601 diabetes mellitus Diseases 0.000 claims description 6
- 239000000960 hypophysis hormone Substances 0.000 claims description 6
- 238000012423 maintenance Methods 0.000 claims description 6
- 208000010125 myocardial infarction Diseases 0.000 claims description 6
- 230000000955 neuroendocrine Effects 0.000 claims description 6
- 230000000926 neurological effect Effects 0.000 claims description 6
- 230000006872 improvement Effects 0.000 claims description 5
- 208000030159 metabolic disease Diseases 0.000 claims description 5
- 229910052760 oxygen Inorganic materials 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 9
- 229910006069 SO3H Inorganic materials 0.000 claims 2
- JLOIWHWGPIRXBQ-UHFFFAOYSA-N 1-(5-methylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amine Chemical compound C=12C(C)=CSC2=NC=NC=1N1CCC(N)CC1 JLOIWHWGPIRXBQ-UHFFFAOYSA-N 0.000 claims 1
- HIRSDTQHJHCMSL-UHFFFAOYSA-N 1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amine Chemical compound C1CC(N)CCN1C1=NC=NC2=C1C(C=1C=CC=CC=1)=CS2 HIRSDTQHJHCMSL-UHFFFAOYSA-N 0.000 claims 1
- MEKFJONRNFOZBD-UHFFFAOYSA-N 1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-one Chemical compound C1CC(=O)CCN1C1=NC=NC2=C1C(C=1C=CC=CC=1)=CS2 MEKFJONRNFOZBD-UHFFFAOYSA-N 0.000 claims 1
- VLCVHCJARZAQOT-UHFFFAOYSA-N 1-(6-methyl-5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amine Chemical compound C=12C(C=3C=CC=CC=3)=C(C)SC2=NC=NC=1N1CCC(N)CC1 VLCVHCJARZAQOT-UHFFFAOYSA-N 0.000 claims 1
- ZCGQJNHNULHCGN-UHFFFAOYSA-N 1-(6-methyl-5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-one Chemical compound C=12C(C=3C=CC=CC=3)=C(C)SC2=NC=NC=1N1CCC(=O)CC1 ZCGQJNHNULHCGN-UHFFFAOYSA-N 0.000 claims 1
- WPZQFXGPJKULGO-UHFFFAOYSA-N 1-[5-(4-bromophenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-amine Chemical compound C1CC(N)CCN1C1=NC=NC2=C1C(C=1C=CC(Br)=CC=1)=CS2 WPZQFXGPJKULGO-UHFFFAOYSA-N 0.000 claims 1
- MBSDVCRHBCVPOE-UHFFFAOYSA-N 1-[5-(4-bromophenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-one Chemical compound C1=CC(Br)=CC=C1C1=CSC2=NC=NC(N3CCC(=O)CC3)=C12 MBSDVCRHBCVPOE-UHFFFAOYSA-N 0.000 claims 1
- OVUIZPTUHKPUQH-UHFFFAOYSA-N 1-[5-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-amine Chemical compound C1=CC(C)=CC=C1C1=CSC2=NC=NC(N3CCC(N)CC3)=C12 OVUIZPTUHKPUQH-UHFFFAOYSA-N 0.000 claims 1
- JPDCBVOCAONAFB-UHFFFAOYSA-N 1-[5-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-one Chemical compound C1=CC(C)=CC=C1C1=CSC2=NC=NC(N3CCC(=O)CC3)=C12 JPDCBVOCAONAFB-UHFFFAOYSA-N 0.000 claims 1
- MJILZRSAPALVKX-UHFFFAOYSA-N 1-phenylmethoxy-3-[[1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]amino]propan-2-ol Chemical compound C=1C=CC=CC=1COCC(O)CNC(CC1)CCN1C(C1=2)=NC=NC=2SC=C1C1=CC=CC=C1 MJILZRSAPALVKX-UHFFFAOYSA-N 0.000 claims 1
- KULJWIMKNZHLIB-UHFFFAOYSA-N 2-[[1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]amino]cyclohexan-1-ol Chemical compound OC1CCCCC1NC1CCN(C=2C=3C(C=4C=CC=CC=4)=CSC=3N=CN=2)CC1 KULJWIMKNZHLIB-UHFFFAOYSA-N 0.000 claims 1
- OEZMHZCSLLPKBL-UHFFFAOYSA-N 2-[[1-(6-methyl-5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]amino]cyclohexan-1-ol Chemical compound C=12C(C=3C=CC=CC=3)=C(C)SC2=NC=NC=1N(CC1)CCC1NC1CCCCC1O OEZMHZCSLLPKBL-UHFFFAOYSA-N 0.000 claims 1
- NOWQHVUBAUZKBW-UHFFFAOYSA-N 2-[[1-[5-(4-bromophenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-yl]amino]cyclohexan-1-ol Chemical compound OC1CCCCC1NC1CCN(C=2C=3C(C=4C=CC(Br)=CC=4)=CSC=3N=CN=2)CC1 NOWQHVUBAUZKBW-UHFFFAOYSA-N 0.000 claims 1
- DCSYMNXHBSHWGF-UHFFFAOYSA-N 2-[[1-[5-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-yl]amino]cyclohexan-1-ol Chemical compound C1=CC(C)=CC=C1C1=CSC2=NC=NC(N3CCC(CC3)NC3C(CCCC3)O)=C12 DCSYMNXHBSHWGF-UHFFFAOYSA-N 0.000 claims 1
- LMANXXYOVPNSPX-UHFFFAOYSA-N 2-[[[1-[5-(4-bromophenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-yl]amino]methyl]-6-fluorophenol Chemical compound OC1=C(F)C=CC=C1CNC1CCN(C=2C=3C(C=4C=CC(Br)=CC=4)=CSC=3N=CN=2)CC1 LMANXXYOVPNSPX-UHFFFAOYSA-N 0.000 claims 1
- AJFKKJXKBSDZIM-UHFFFAOYSA-N 2-benzyl-5-methyl-4-morpholin-4-ylthieno[2,3-d]pyrimidine-6-carbonitrile Chemical compound N=1C(N2CCOCC2)=C2C(C)=C(C#N)SC2=NC=1CC1=CC=CC=C1 AJFKKJXKBSDZIM-UHFFFAOYSA-N 0.000 claims 1
- AATLCSFFWZGMQU-UHFFFAOYSA-N 2-fluoro-6-[[[1-(6-methyl-5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]amino]methyl]phenol Chemical compound C=12C(C=3C=CC=CC=3)=C(C)SC2=NC=NC=1N(CC1)CCC1NCC1=CC=CC(F)=C1O AATLCSFFWZGMQU-UHFFFAOYSA-N 0.000 claims 1
- PYPSXRCWZBICRL-UHFFFAOYSA-N 5-methoxy-2-[[[1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]amino]methyl]phenol Chemical compound OC1=CC(OC)=CC=C1CNC1CCN(C=2C=3C(C=4C=CC=CC=4)=CSC=3N=CN=2)CC1 PYPSXRCWZBICRL-UHFFFAOYSA-N 0.000 claims 1
- XELONUDAUWADKG-UHFFFAOYSA-N CC(C=C1)=CC=C1C1=CSC2=NC=NC(N(CC3)CCC3NCC3=CC=CC(F)=C3O)=C12.OC(CNC(CC1)CCN1C1=NC=NC2=C1C(C1=CC=CC=C1)=CS2)COCC1=CC=CC=C1 Chemical compound CC(C=C1)=CC=C1C1=CSC2=NC=NC(N(CC3)CCC3NCC3=CC=CC(F)=C3O)=C12.OC(CNC(CC1)CCN1C1=NC=NC2=C1C(C1=CC=CC=C1)=CS2)COCC1=CC=CC=C1 XELONUDAUWADKG-UHFFFAOYSA-N 0.000 claims 1
- ZVNNEBMZOWYGFP-UHFFFAOYSA-N n,n-bis[(2-fluorophenyl)methyl]-1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-amine Chemical compound FC1=CC=CC=C1CN(C1CCN(CC1)C=1C=2C(C=3C=CC=CC=3)=CSC=2N=CN=1)CC1=CC=CC=C1F ZVNNEBMZOWYGFP-UHFFFAOYSA-N 0.000 claims 1
- XQHDQCRNRSAGPV-UHFFFAOYSA-N tert-butyl n-[1-(5-methylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]carbamate Chemical compound C=12C(C)=CSC2=NC=NC=1N1CCC(NC(=O)OC(C)(C)C)CC1 XQHDQCRNRSAGPV-UHFFFAOYSA-N 0.000 claims 1
- DENZKSMZADASCI-UHFFFAOYSA-N tert-butyl n-[1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]carbamate Chemical compound C1CC(NC(=O)OC(C)(C)C)CCN1C1=NC=NC2=C1C(C=1C=CC=CC=1)=CS2 DENZKSMZADASCI-UHFFFAOYSA-N 0.000 claims 1
- NESAZZCPNCLODA-UHFFFAOYSA-N tert-butyl n-[1-(6-methyl-5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]carbamate Chemical compound C=12C(C=3C=CC=CC=3)=C(C)SC2=NC=NC=1N1CCC(NC(=O)OC(C)(C)C)CC1 NESAZZCPNCLODA-UHFFFAOYSA-N 0.000 claims 1
- XLJSUFGVURYUEV-UHFFFAOYSA-N tert-butyl n-[1-[5-(4-methylphenyl)thieno[2,3-d]pyrimidin-4-yl]piperidin-4-yl]carbamate Chemical compound C1=CC(C)=CC=C1C1=CSC2=NC=NC(N3CCC(CC3)NC(=O)OC(C)(C)C)=C12 XLJSUFGVURYUEV-UHFFFAOYSA-N 0.000 claims 1
- 102100033063 G protein-activated inward rectifier potassium channel 1 Human genes 0.000 abstract description 35
- 101000944266 Homo sapiens G protein-activated inward rectifier potassium channel 1 Proteins 0.000 abstract description 35
- 101000614712 Homo sapiens G protein-activated inward rectifier potassium channel 4 Proteins 0.000 abstract description 18
- 102100021237 G protein-activated inward rectifier potassium channel 4 Human genes 0.000 abstract description 16
- 229910052740 iodine Inorganic materials 0.000 abstract description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 222
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 194
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 178
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 152
- 238000006243 chemical reaction Methods 0.000 description 151
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 143
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 118
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 96
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 96
- DDWBRNXDKNIQDY-UHFFFAOYSA-N thieno[2,3-d]pyrimidine Chemical class N1=CN=C2SC=CC2=C1 DDWBRNXDKNIQDY-UHFFFAOYSA-N 0.000 description 95
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 75
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 69
- 239000002904 solvent Substances 0.000 description 64
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 63
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 56
- 229910003827 NRaRb Inorganic materials 0.000 description 55
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 53
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 50
- 239000000243 solution Substances 0.000 description 49
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 44
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 42
- 239000007858 starting material Substances 0.000 description 42
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- 230000015572 biosynthetic process Effects 0.000 description 33
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- 150000003839 salts Chemical class 0.000 description 20
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 19
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- 125000003545 alkoxy group Chemical group 0.000 description 18
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- GKPIFULDHDHNBW-UHFFFAOYSA-N thieno[2,3-d]pyrimidine-6-carboxamide Chemical compound N1=CN=C2SC(C(=O)N)=CC2=C1 GKPIFULDHDHNBW-UHFFFAOYSA-N 0.000 description 18
- 125000004429 atom Chemical group 0.000 description 17
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- 238000002953 preparative HPLC Methods 0.000 description 17
- 101100063435 Caenorhabditis elegans din-1 gene Proteins 0.000 description 16
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 16
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 16
- KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 description 16
- VLJNHYLEOZPXFW-UHFFFAOYSA-N pyrrolidine-2-carboxamide Chemical compound NC(=O)C1CCCN1 VLJNHYLEOZPXFW-UHFFFAOYSA-N 0.000 description 16
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- 239000004480 active ingredient Substances 0.000 description 14
- NRAOLILGQIRZBT-UHFFFAOYSA-N thieno[2,3-d]pyrimidin-2-amine Chemical compound NC1=NC=C2C=CSC2=N1 NRAOLILGQIRZBT-UHFFFAOYSA-N 0.000 description 14
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Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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- A61P9/06—Antiarrhythmics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
- C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
- C07D491/048—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1119703.5A GB201119703D0 (en) | 2011-11-15 | 2011-11-15 | Compounds |
| GB1119703.5 | 2011-11-15 | ||
| GB1214250.1 | 2012-08-09 | ||
| GBGB1214250.1A GB201214250D0 (en) | 2012-08-09 | 2012-08-09 | Compounds |
| PCT/GB2012/052842 WO2013072694A1 (en) | 2011-11-15 | 2012-11-15 | Thieno- and furo - pyrimidines and pyridines, useful as potassium channel inhibitors |
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| Publication Number | Publication Date |
|---|---|
| CA2855346A1 true CA2855346A1 (en) | 2013-05-23 |
Family
ID=47222145
Family Applications (1)
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| CA2855346A Abandoned CA2855346A1 (en) | 2011-11-15 | 2012-11-15 | Thieno- and furo - pyrimidines and pyridines, useful as potassium channel inhibitors |
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| RU2667507C2 (ru) | 2013-06-06 | 2018-09-21 | Астеллас Фарма Инк. | Бензотиофеновое соединение |
| FR3015483B1 (fr) * | 2013-12-23 | 2016-01-01 | Servier Lab | Nouveaux derives de thienopyrimidine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| RU2545758C1 (ru) * | 2014-03-20 | 2015-04-10 | Общество с ограниченной ответственностью "Алион" | Бициклические пиримидины или их фармацевтически приемлемые соли-активаторы антиоксидантной программы и их применение в качестве цитопротекторов |
| WO2016040330A1 (en) | 2014-09-09 | 2016-03-17 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| TWI703150B (zh) | 2015-06-04 | 2020-09-01 | 美商庫拉腫瘤技術股份有限公司 | 用於抑制ｍｅｎｉｎ及ｍｌｌ蛋白之交互作用的方法及組合物 |
| US10588907B2 (en) | 2015-06-04 | 2020-03-17 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| FR3037956B1 (fr) * | 2015-06-23 | 2017-08-04 | Servier Lab | Nouveaux derives d'acide amine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR3037957B1 (fr) * | 2015-06-23 | 2019-01-25 | Les Laboratoires Servier | Nouveaux derives d'hydroxyester, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR3037958B1 (fr) * | 2015-06-23 | 2019-01-25 | Les Laboratoires Servier | Nouveaux derives d'hydroxy-acide, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| FR3037959B1 (fr) * | 2015-06-23 | 2017-08-04 | Servier Lab | Nouveaux derives bicycliques, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| CA3008171A1 (en) | 2015-12-22 | 2017-06-29 | SHY Therapeutics LLC | Compounds for the treatment of cancer and inflammatory disease |
| PH12018501955B1 (en) | 2016-03-16 | 2024-01-24 | Kura Oncology Inc | Bridged bicyclic inhibitors of menin-mll and methods of use |
| SI3429591T1 (sl) * | 2016-03-16 | 2023-07-31 | Kura Oncology, Inc. | Substituirani tieno(2,3-d)pirimidinski derivati kot inhibitorji menin-MLL in postopki uporabe |
| CN106727587A (zh) * | 2016-11-28 | 2017-05-31 | 李娜 | 一种治疗心律失常的药物组合物 |
| EP3562828A1 (en) | 2016-12-28 | 2019-11-06 | Dart NeuroScience LLC | Substituted pyrazolopyrimidinone compounds as pde2 inhibitors |
| EA038388B1 (ru) * | 2017-01-16 | 2021-08-19 | Кура Онколоджи, Инк. | Замещенные ингибиторы менина-mll и способы применения |
| CN110691779B (zh) | 2017-03-24 | 2023-10-10 | 库拉肿瘤学公司 | 治疗血液系统恶性肿瘤和尤因肉瘤的方法 |
| US11542248B2 (en) | 2017-06-08 | 2023-01-03 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with MLL proteins |
| WO2018237084A1 (en) | 2017-06-21 | 2018-12-27 | SHY Therapeutics LLC | COMPOUNDS INTERACTING WITH RAS SUPERFAMIL FOR USE IN THE TREATMENT OF CANCERS, INFLAMMATORY DISEASES, RASOPATHIES AND FIBROTIC DISEASES |
| CA3072648A1 (en) * | 2017-08-14 | 2019-02-21 | Acesion Pharma Aps | Substituted benzimidazoles as potassium channel inhibitors |
| WO2019060365A1 (en) | 2017-09-20 | 2019-03-28 | Kura Oncology, Inc. | SUBSTITUTED MÉNINE-MLL INHIBITORS AND METHODS OF USE |
| WO2019104285A1 (en) | 2017-11-27 | 2019-05-31 | Dart Neuroscience, Llc | Substituted furanopyrimidine compounds as pde1 inhibitors |
| CN108117556A (zh) * | 2018-01-15 | 2018-06-05 | 王山川 | 一种细胞周期检查点激酶1抑制剂的合成方法 |
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| JP7407461B2 (ja) | 2018-12-19 | 2024-01-04 | シャイ・セラピューティクス・エルエルシー | がん、炎症性疾患、ｒａｓ病、及び線維性疾患の処置のためのｒａｓスーパーファミリーと相互作用する化合物 |
| JP7458406B2 (ja) | 2018-12-21 | 2024-03-29 | セルジーン コーポレーション | Ｒｉｐｋ２のチエノピリジン阻害剤 |
| MX2022005053A (es) | 2019-10-28 | 2022-05-18 | Merck Sharp & Dohme Llc | Inhibidores de peque?as moleculas de mutante g12c de kras. |
| WO2021106231A1 (en) * | 2019-11-29 | 2021-06-03 | Taiho Pharmaceutical Co., Ltd. | A compound having inhibitory activity against kras g12d mutation |
| WO2021106230A1 (ja) | 2019-11-29 | 2021-06-03 | 大鵬薬品工業株式会社 | 新規なフェノール化合物又はその塩 |
| WO2022194191A1 (en) * | 2021-03-16 | 2022-09-22 | Guangdong Newopp Biopharmaceuticals Co., Ltd. | Heterocyclic compounds as inhibitors of kras g12d |
| EP4313973A1 (en) * | 2021-03-22 | 2024-02-07 | Acesion Pharma ApS | Novel potassium channel inhibitors |
| TW202304925A (zh) * | 2021-03-26 | 2023-02-01 | 美商住友製藥腫瘤公司 | （呋喃并嘧啶—４—基）哌𠯤化合物及其用途 |
| CN115006468B (zh) * | 2022-06-28 | 2023-06-06 | 西安外事学院 | 一种复方中草药生发液及制备方法 |
| TW202535891A (zh) | 2023-10-20 | 2025-09-16 | 美商默沙東有限責任公司 | Ｋｒａｓ蛋白之小分子抑制劑 |
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2012
- 2012-11-14 AR ARP120104296A patent/AR090037A1/es unknown
- 2012-11-15 MX MX2014005935A patent/MX2014005935A/es not_active Application Discontinuation
- 2012-11-15 TW TW101142693A patent/TWI498331B/zh not_active IP Right Cessation
- 2012-11-15 WO PCT/GB2012/052842 patent/WO2013072694A1/en not_active Ceased
- 2012-11-15 CA CA2855346A patent/CA2855346A1/en not_active Abandoned
- 2012-11-15 JP JP2014540560A patent/JP2014533259A/ja active Pending
- 2012-11-15 US US14/358,722 patent/US9290511B2/en not_active Expired - Fee Related
- 2012-11-15 AU AU2012338570A patent/AU2012338570A1/en not_active Abandoned
- 2012-11-15 RU RU2014124101/04A patent/RU2014124101A/ru not_active Application Discontinuation
- 2012-11-15 CN CN201280061286.3A patent/CN104011054B/zh not_active Expired - Fee Related
- 2012-11-15 EP EP12790948.9A patent/EP2780343A1/en not_active Withdrawn
- 2012-11-15 IN IN1183MUN2014 patent/IN2014MN01183A/en unknown
- 2012-11-15 KR KR1020147015757A patent/KR20140094603A/ko not_active Withdrawn
- 2012-11-15 BR BR112014011671A patent/BR112014011671A2/pt not_active IP Right Cessation
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2014
- 2014-05-14 ZA ZA2014/03503A patent/ZA201403503B/en unknown
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2016
- 2016-02-05 US US15/016,846 patent/US20160152634A1/en not_active Abandoned
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| CN104011054B (zh) | 2016-08-24 |
| RU2014124101A (ru) | 2015-12-27 |
| US20160152634A1 (en) | 2016-06-02 |
| BR112014011671A2 (pt) | 2017-05-30 |
| ZA201403503B (en) | 2016-09-28 |
| IN2014MN01183A (cg-RX-API-DMAC7.html) | 2015-07-03 |
| AU2012338570A1 (en) | 2014-07-03 |
| TWI498331B (zh) | 2015-09-01 |
| TW201326178A (zh) | 2013-07-01 |
| US20140371203A1 (en) | 2014-12-18 |
| CN104011054A (zh) | 2014-08-27 |
| MX2014005935A (es) | 2014-09-04 |
| KR20140094603A (ko) | 2014-07-30 |
| WO2013072694A1 (en) | 2013-05-23 |
| JP2014533259A (ja) | 2014-12-11 |
| NZ626199A (en) | 2015-04-24 |
| AR090037A1 (es) | 2014-10-15 |
| EP2780343A1 (en) | 2014-09-24 |
| US9290511B2 (en) | 2016-03-22 |
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Effective date: 20171115 |