JP2014533259A - カリウムチャネル阻害剤として有用なチエノおよびフロピリミジンならびにピリジン - Google Patents
カリウムチャネル阻害剤として有用なチエノおよびフロピリミジンならびにピリジン Download PDFInfo
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- JP2014533259A JP2014533259A JP2014540560A JP2014540560A JP2014533259A JP 2014533259 A JP2014533259 A JP 2014533259A JP 2014540560 A JP2014540560 A JP 2014540560A JP 2014540560 A JP2014540560 A JP 2014540560A JP 2014533259 A JP2014533259 A JP 2014533259A
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- JP
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- Prior art keywords
- alkyl
- optionally substituted
- thieno
- pyrimidin
- 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.)
- Pending
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- 239000003112 inhibitor Substances 0.000 title abstract description 21
- 102000004257 Potassium Channel Human genes 0.000 title abstract description 9
- 108020001213 potassium channel Proteins 0.000 title abstract description 9
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title description 20
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 title description 10
- RBNBDIMXFJYDLQ-UHFFFAOYSA-N thieno[3,2-d]pyrimidine Chemical group C1=NC=C2SC=CC2=N1 RBNBDIMXFJYDLQ-UHFFFAOYSA-N 0.000 title description 4
- JUQAECQBUNODQP-UHFFFAOYSA-N furo[3,2-d]pyrimidine Chemical compound C1=NC=C2OC=CC2=N1 JUQAECQBUNODQP-UHFFFAOYSA-N 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 321
- 238000011282 treatment Methods 0.000 claims abstract description 76
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 45
- 201000010099 disease Diseases 0.000 claims abstract description 29
- 230000005764 inhibitory process Effects 0.000 claims abstract description 29
- 238000002560 therapeutic procedure Methods 0.000 claims abstract description 15
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 514
- -1 substituted Chemical class 0.000 claims description 356
- 125000000547 substituted alkyl group Chemical group 0.000 claims description 125
- 238000000034 method Methods 0.000 claims description 124
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 112
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 89
- 239000000203 mixture Substances 0.000 claims description 82
- 125000001072 heteroaryl group Chemical group 0.000 claims description 62
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims description 61
- 206010003658 Atrial Fibrillation Diseases 0.000 claims description 60
- 239000003814 drug Substances 0.000 claims description 54
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 54
- 125000003386 piperidinyl group Chemical group 0.000 claims description 53
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 52
- 125000005843 halogen group Chemical group 0.000 claims description 52
- 229910052757 nitrogen Inorganic materials 0.000 claims description 51
- 125000002947 alkylene group Chemical group 0.000 claims description 44
- 125000005415 substituted alkoxy group Chemical group 0.000 claims description 43
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 38
- 229910052760 oxygen Inorganic materials 0.000 claims description 35
- 125000003107 substituted aryl group Chemical group 0.000 claims description 35
- 125000003118 aryl group Chemical group 0.000 claims description 33
- 230000001746 atrial effect Effects 0.000 claims description 30
- 125000002757 morpholinyl group Chemical group 0.000 claims description 29
- 229910052717 sulfur Inorganic materials 0.000 claims description 28
- 125000001424 substituent group Chemical group 0.000 claims description 26
- 230000001404 mediated effect Effects 0.000 claims description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 23
- 230000004064 dysfunction Effects 0.000 claims description 21
- 206010003662 Atrial flutter Diseases 0.000 claims description 19
- 125000003545 alkoxy group Chemical group 0.000 claims description 19
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 19
- 230000002265 prevention Effects 0.000 claims description 18
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 17
- 229940079593 drug Drugs 0.000 claims description 16
- 208000035475 disorder Diseases 0.000 claims description 15
- 208000001435 Thromboembolism 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
- 210000001013 sinoatrial node Anatomy 0.000 claims description 14
- 125000004953 trihalomethyl group Chemical group 0.000 claims description 14
- 125000005885 heterocycloalkylalkyl group Chemical group 0.000 claims description 13
- 125000005968 oxazolinyl group Chemical group 0.000 claims description 13
- 125000006004 trihaloethyl group Chemical group 0.000 claims description 13
- 206010042600 Supraventricular arrhythmias Diseases 0.000 claims description 12
- 125000004171 alkoxy aryl group Chemical group 0.000 claims description 11
- 125000005530 alkylenedioxy group Chemical group 0.000 claims description 11
- 125000004366 heterocycloalkenyl group Chemical group 0.000 claims description 11
- 208000006011 Stroke Diseases 0.000 claims description 10
- 125000002393 azetidinyl group Chemical group 0.000 claims description 10
- 125000003725 azepanyl group Chemical group 0.000 claims description 9
- 230000000747 cardiac effect Effects 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 125000006008 trihaloethoxy group Chemical group 0.000 claims description 9
- 125000004951 trihalomethoxy group Chemical group 0.000 claims description 9
- 229910052720 vanadium Inorganic materials 0.000 claims description 9
- 208000005189 Embolism Diseases 0.000 claims description 8
- 208000002193 Pain Diseases 0.000 claims description 8
- 208000007536 Thrombosis Diseases 0.000 claims description 8
- 206010015037 epilepsy Diseases 0.000 claims description 8
- 125000005842 heteroatom Chemical group 0.000 claims description 8
- 230000036407 pain Effects 0.000 claims description 8
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- 230000028327 secretion 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
- 206010040639 Sick sinus syndrome Diseases 0.000 claims description 7
- 230000006870 function Effects 0.000 claims description 7
- 238000012423 maintenance Methods 0.000 claims description 7
- 208000010125 myocardial infarction Diseases 0.000 claims description 7
- 238000007634 remodeling Methods 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
- 206010028980 Neoplasm Diseases 0.000 claims description 6
- 208000018262 Peripheral vascular disease Diseases 0.000 claims description 6
- 230000036506 anxiety Effects 0.000 claims description 6
- 230000011128 cardiac conduction Effects 0.000 claims description 6
- 206010012601 diabetes mellitus Diseases 0.000 claims description 6
- 208000013403 hyperactivity Diseases 0.000 claims description 6
- 239000000960 hypophysis hormone Substances 0.000 claims description 6
- 230000000926 neurological effect Effects 0.000 claims description 6
- 238000002360 preparation method Methods 0.000 claims description 6
- 210000001992 atrioventricular node Anatomy 0.000 claims description 5
- 201000011510 cancer Diseases 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 230000006872 improvement Effects 0.000 claims description 5
- 208000030159 metabolic disease Diseases 0.000 claims description 5
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 4
- 210000005036 nerve Anatomy 0.000 claims description 4
- 230000000955 neuroendocrine Effects 0.000 claims description 4
- 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 description 3
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 3
- 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 description 2
- 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 description 2
- FGBZVXXVBHTVOP-UHFFFAOYSA-N 2-(1,3-benzodioxol-5-yloxymethyl)-4-[1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]morpholine Chemical compound C=1C=C2OCOC2=CC=1OCC(OCC1)CN1C(CC1)CCN1C(C1=2)=NC=NC=2SC=C1C1=CC=CC=C1 FGBZVXXVBHTVOP-UHFFFAOYSA-N 0.000 claims description 2
- 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 description 2
- DQRYKEHGQJTOES-UHFFFAOYSA-N 6-(1,3-benzodioxol-5-yloxymethyl)-4-[1-(5-phenylthieno[2,3-d]pyrimidin-4-yl)piperidin-4-yl]morpholin-3-one Chemical compound O=C1COC(COC=2C=C3OCOC3=CC=2)CN1C(CC1)CCN1C(C1=2)=NC=NC=2SC=C1C1=CC=CC=C1 DQRYKEHGQJTOES-UHFFFAOYSA-N 0.000 claims description 2
- 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 description 2
- 230000033228 biological regulation Effects 0.000 claims 5
- 230000007368 endocrine function Effects 0.000 claims 2
- 230000003557 neuropsychological effect Effects 0.000 claims 2
- 102100033063 G protein-activated inward rectifier potassium channel 1 Human genes 0.000 abstract description 3
- 102100021237 G protein-activated inward rectifier potassium channel 4 Human genes 0.000 abstract description 3
- 101000944266 Homo sapiens G protein-activated inward rectifier potassium channel 1 Proteins 0.000 abstract description 3
- 101000614712 Homo sapiens G protein-activated inward rectifier potassium channel 4 Proteins 0.000 abstract description 3
- 238000006243 chemical reaction Methods 0.000 description 192
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 185
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 172
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 128
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 128
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 102
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 93
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 84
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 79
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 73
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 64
- 239000002904 solvent Substances 0.000 description 61
- 230000007246 mechanism Effects 0.000 description 54
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 51
- 239000000243 solution Substances 0.000 description 49
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 48
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 47
- 235000019439 ethyl acetate Nutrition 0.000 description 45
- 239000007858 starting material Substances 0.000 description 40
- 238000010992 reflux Methods 0.000 description 39
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 36
- 239000002585 base Substances 0.000 description 35
- 239000007787 solid Substances 0.000 description 35
- 238000010561 standard procedure Methods 0.000 description 34
- 239000000126 substance Substances 0.000 description 34
- HTELSLAJWRHNRH-UHFFFAOYSA-N 2-cyclopropyl-5-(2-methoxyphenyl)-4-[4-(2-pyrrolidin-1-ylethoxymethyl)piperidin-1-yl]thieno[2,3-d]pyrimidine Chemical compound COC1=CC=CC=C1C1=CSC2=NC(C3CC3)=NC(N3CCC(COCCN4CCCC4)CC3)=C12 HTELSLAJWRHNRH-UHFFFAOYSA-N 0.000 description 33
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 31
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- 229940124597 therapeutic agent Drugs 0.000 description 29
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- 229910052799 carbon Inorganic materials 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
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- 125000004432 carbon atom Chemical group C* 0.000 description 21
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 20
- 239000002253 acid Substances 0.000 description 20
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- 150000003839 salts Chemical class 0.000 description 19
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 18
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- 125000004193 piperazinyl group Chemical group 0.000 description 14
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 13
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 13
- 125000000753 cycloalkyl group Chemical group 0.000 description 13
- 230000000694 effects Effects 0.000 description 13
- 238000002953 preparative HPLC Methods 0.000 description 13
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 13
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide Chemical compound CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 12
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 12
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- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 12
- DDWBRNXDKNIQDY-UHFFFAOYSA-N thieno[2,3-d]pyrimidine Chemical class N1=CN=C2SC=CC2=C1 DDWBRNXDKNIQDY-UHFFFAOYSA-N 0.000 description 12
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- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 10
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- YLDJMNFQDUEVHZ-UHFFFAOYSA-N 4-(2-pyrrolidin-1-ylethoxymethyl)piperidine Chemical compound C1CNCCC1COCCN1CCCC1 YLDJMNFQDUEVHZ-UHFFFAOYSA-N 0.000 description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 9
- 108091006146 Channels Proteins 0.000 description 9
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- 238000004128 high performance liquid chromatography Methods 0.000 description 9
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- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 8
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 8
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- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
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- 241000894007 species Species 0.000 description 8
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- WONOKVSIDWOIGC-UHFFFAOYSA-N 4-chloro-5-phenylthieno[2,3-d]pyrimidine Chemical compound C1=2C(Cl)=NC=NC=2SC=C1C1=CC=CC=C1 WONOKVSIDWOIGC-UHFFFAOYSA-N 0.000 description 7
- 206010003130 Arrhythmia supraventricular Diseases 0.000 description 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 7
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 7
- 108090000862 Ion Channels Proteins 0.000 description 7
- 102000004310 Ion Channels Human genes 0.000 description 7
- MUXRDTRNJAJOPS-UHFFFAOYSA-N [8-(4-morpholin-4-yl-5-phenylthieno[2,3-d]pyrimidin-2-yl)-8-azabicyclo[3.2.1]octan-3-yl]methanol Chemical compound C1C(CO)CC2CCC1N2C(N=C1SC=C(C1=1)C=2C=CC=CC=2)=NC=1N1CCOCC1 MUXRDTRNJAJOPS-UHFFFAOYSA-N 0.000 description 7
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- 238000004587 chromatography analysis Methods 0.000 description 7
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- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 7
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- ACIDWYRSUDNYPE-UHFFFAOYSA-N n-[5-phenyl-2-[4-(2-pyrrolidin-1-ylethoxymethyl)piperidin-1-yl]thieno[2,3-d]pyrimidin-6-yl]acetamide Chemical compound CC(=O)NC=1SC2=NC(N3CCC(COCCN4CCCC4)CC3)=NC=C2C=1C1=CC=CC=C1 ACIDWYRSUDNYPE-UHFFFAOYSA-N 0.000 description 7
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- CTEDVGRUGMPBHE-UHFFFAOYSA-N tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(CO)CC1 CTEDVGRUGMPBHE-UHFFFAOYSA-N 0.000 description 1
- HDPGSWMTDGGUEB-UHFFFAOYSA-N tert-butyl 5-hydroxy-2-azabicyclo[2.2.1]heptane-2-carboxylate Chemical compound C1C2N(C(=O)OC(C)(C)C)CC1C(O)C2 HDPGSWMTDGGUEB-UHFFFAOYSA-N 0.000 description 1
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- 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 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 description 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 description 1
- 125000003507 tetrahydrothiofenyl group Chemical group 0.000 description 1
- 125000004632 tetrahydrothiopyranyl group Chemical group S1C(CCCC1)* 0.000 description 1
- UEUXEKPTXMALOB-UHFFFAOYSA-J tetrasodium;2-[2-[bis(carboxylatomethyl)amino]ethyl-(carboxylatomethyl)amino]acetate Chemical compound [Na+].[Na+].[Na+].[Na+].[O-]C(=O)CN(CC([O-])=O)CCN(CC([O-])=O)CC([O-])=O UEUXEKPTXMALOB-UHFFFAOYSA-J 0.000 description 1
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- SMZMHUCIDGHERP-UHFFFAOYSA-N thieno[2,3-b]pyridine Chemical class C1=CN=C2SC=CC2=C1 SMZMHUCIDGHERP-UHFFFAOYSA-N 0.000 description 1
- HACJQZHGTLOKSH-UHFFFAOYSA-N thieno[2,3-d]pyrimidine-6-carboxylic acid Chemical compound N1=CN=C2SC(C(=O)O)=CC2=C1 HACJQZHGTLOKSH-UHFFFAOYSA-N 0.000 description 1
- DBDCNCCRPKTRSD-UHFFFAOYSA-N thieno[3,2-b]pyridine Chemical compound C1=CC=C2SC=CC2=N1 DBDCNCCRPKTRSD-UHFFFAOYSA-N 0.000 description 1
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- VHBFFQKBGNRLFZ-UHFFFAOYSA-N vitamin p Natural products O1C2=CC=CC=C2C(=O)C=C1C1=CC=CC=C1 VHBFFQKBGNRLFZ-UHFFFAOYSA-N 0.000 description 1
- PJVWKTKQMONHTI-UHFFFAOYSA-N warfarin Chemical compound OC=1C2=CC=CC=C2OC(=O)C=1C(CC(=O)C)C1=CC=CC=C1 PJVWKTKQMONHTI-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- 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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- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- 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
Landscapes
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- Hematology (AREA)
- Emergency Medicine (AREA)
- Psychiatry (AREA)
- Reproductive Health (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
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|---|---|---|---|
| GB1119703.5 | 2011-11-15 | ||
| GBGB1119703.5A GB201119703D0 (en) | 2011-11-15 | 2011-11-15 | Compounds |
| GBGB1214250.1A GB201214250D0 (en) | 2012-08-09 | 2012-08-09 | Compounds |
| GB1214250.1 | 2012-08-09 | ||
| PCT/GB2012/052842 WO2013072694A1 (en) | 2011-11-15 | 2012-11-15 | Thieno- and furo - pyrimidines and pyridines, useful as potassium channel inhibitors |
Publications (2)
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| JP2014533259A true JP2014533259A (ja) | 2014-12-11 |
| JP2014533259A5 JP2014533259A5 (enEXAMPLES) | 2016-01-14 |
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| US (2) | US9290511B2 (enEXAMPLES) |
| EP (1) | EP2780343A1 (enEXAMPLES) |
| JP (1) | JP2014533259A (enEXAMPLES) |
| KR (1) | KR20140094603A (enEXAMPLES) |
| CN (1) | CN104011054B (enEXAMPLES) |
| AR (1) | AR090037A1 (enEXAMPLES) |
| AU (1) | AU2012338570A1 (enEXAMPLES) |
| BR (1) | BR112014011671A2 (enEXAMPLES) |
| CA (1) | CA2855346A1 (enEXAMPLES) |
| IN (1) | IN2014MN01183A (enEXAMPLES) |
| MX (1) | MX2014005935A (enEXAMPLES) |
| RU (1) | RU2014124101A (enEXAMPLES) |
| TW (1) | TWI498331B (enEXAMPLES) |
| WO (1) | WO2013072694A1 (enEXAMPLES) |
| ZA (1) | ZA201403503B (enEXAMPLES) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
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| JP2018522855A (ja) * | 2015-06-23 | 2018-08-16 | レ ラボラトワール セルヴィエ | 新規なヒドロキシエステル誘導体、その調製方法及びそれを含有する医薬組成物 |
| JP2018522856A (ja) * | 2015-06-23 | 2018-08-16 | レ ラボラトワール セルヴィエ | 新規なアミノ酸誘導体、その製造方法、及びそれを含有する医薬組成物 |
| JP2018527296A (ja) * | 2015-06-23 | 2018-09-20 | レ ラボラトワール セルヴィエ | 新規なヒドロキシ酸誘導体、その製造方法、及びそれを含有する医薬組成物 |
| JP2018527297A (ja) * | 2015-06-23 | 2018-09-20 | レ ラボラトワール セルヴィエ | 新規な二環式誘導体、それらを調製するためのプロセス及びそれらを含有する医薬組成物 |
| JP2023512113A (ja) * | 2019-11-29 | 2023-03-23 | 大鵬薬品工業株式会社 | Ｋｒａｓ ｇ１２ｄ変異に対して阻害活性を有する化合物 |
| JP2024511101A (ja) * | 2021-03-22 | 2024-03-12 | アセシオン ファーマ エイピーエス | 新規カリウムチャネル阻害剤 |
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| MX2015016743A (es) | 2013-06-06 | 2016-03-21 | Astellas Pharma Inc | Compuesto de benzotiofeno. |
| 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 |
| US10246464B2 (en) | 2014-09-09 | 2019-04-02 | The Regents Of The University Of Michigan | Thienopyrimidine and thienopyridine compounds and methods of use thereof |
| WO2016197027A1 (en) | 2015-06-04 | 2016-12-08 | Kura Oncology, Inc. | Methods and compositions for inhibiting the interaction of menin with mll proteins |
| 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 |
| EP3394056B1 (en) | 2015-12-22 | 2021-04-14 | Shy Therapeutics LLC | Compounds for the treatment of cancer and inflammatory disease |
| MX388839B (es) * | 2016-03-16 | 2025-03-20 | Kura Oncology Inc | Inhibidores sustituidos de menina-mll y metodos de uso |
| SG11201807834WA (en) | 2016-03-16 | 2018-10-30 | Kura Oncology Inc | Bridged bicyclic inhibitors of menin-mll and methods of use |
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| JP2018522855A (ja) * | 2015-06-23 | 2018-08-16 | レ ラボラトワール セルヴィエ | 新規なヒドロキシエステル誘導体、その調製方法及びそれを含有する医薬組成物 |
| JP2018522856A (ja) * | 2015-06-23 | 2018-08-16 | レ ラボラトワール セルヴィエ | 新規なアミノ酸誘導体、その製造方法、及びそれを含有する医薬組成物 |
| JP2018527296A (ja) * | 2015-06-23 | 2018-09-20 | レ ラボラトワール セルヴィエ | 新規なヒドロキシ酸誘導体、その製造方法、及びそれを含有する医薬組成物 |
| JP2018527297A (ja) * | 2015-06-23 | 2018-09-20 | レ ラボラトワール セルヴィエ | 新規な二環式誘導体、それらを調製するためのプロセス及びそれらを含有する医薬組成物 |
| JP2023512113A (ja) * | 2019-11-29 | 2023-03-23 | 大鵬薬品工業株式会社 | Ｋｒａｓ ｇ１２ｄ変異に対して阻害活性を有する化合物 |
| JP7707189B2 (ja) | 2019-11-29 | 2025-07-14 | 大鵬薬品工業株式会社 | Ｋｒａｓ ｇ１２ｄ変異に対して阻害活性を有する化合物 |
| JP2024511101A (ja) * | 2021-03-22 | 2024-03-12 | アセシオン ファーマ エイピーエス | 新規カリウムチャネル阻害剤 |
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| RU2014124101A (ru) | 2015-12-27 |
| AR090037A1 (es) | 2014-10-15 |
| US20160152634A1 (en) | 2016-06-02 |
| NZ626199A (en) | 2015-04-24 |
| CA2855346A1 (en) | 2013-05-23 |
| AU2012338570A1 (en) | 2014-07-03 |
| WO2013072694A1 (en) | 2013-05-23 |
| TW201326178A (zh) | 2013-07-01 |
| US9290511B2 (en) | 2016-03-22 |
| CN104011054A (zh) | 2014-08-27 |
| CN104011054B (zh) | 2016-08-24 |
| US20140371203A1 (en) | 2014-12-18 |
| MX2014005935A (es) | 2014-09-04 |
| KR20140094603A (ko) | 2014-07-30 |
| TWI498331B (zh) | 2015-09-01 |
| EP2780343A1 (en) | 2014-09-24 |
| ZA201403503B (en) | 2016-09-28 |
| IN2014MN01183A (enEXAMPLES) | 2015-07-03 |
| BR112014011671A2 (pt) | 2017-05-30 |
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