JP2015504061A5 - - Google Patents
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- Publication number
- JP2015504061A5 JP2015504061A5 JP2014550525A JP2014550525A JP2015504061A5 JP 2015504061 A5 JP2015504061 A5 JP 2015504061A5 JP 2014550525 A JP2014550525 A JP 2014550525A JP 2014550525 A JP2014550525 A JP 2014550525A JP 2015504061 A5 JP2015504061 A5 JP 2015504061A5
- Authority
- JP
- Japan
- Prior art keywords
- pyridin
- halo
- group
- imidazo
- alkyl
- 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.)
- Granted
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- 125000005843 halogen group Chemical group 0.000 claims 35
- 125000000217 alkyl group Chemical group 0.000 claims 33
- 150000003839 salts Chemical class 0.000 claims 21
- -1 cyano, carboxy Chemical group 0.000 claims 20
- 150000001875 compounds Chemical class 0.000 claims 18
- 125000003342 alkenyl group Chemical group 0.000 claims 14
- 125000000304 alkynyl group Chemical group 0.000 claims 14
- 229910052739 hydrogen Inorganic materials 0.000 claims 14
- 125000001072 heteroaryl group Chemical group 0.000 claims 11
- 239000001257 hydrogen Substances 0.000 claims 10
- FWCVZAQENIZVMY-UHFFFAOYSA-N 2-hydroxy-6-[[2-(2-propan-2-ylpyrazol-3-yl)pyridin-3-yl]methoxy]benzaldehyde Chemical compound CC(C)N1N=CC=C1C1=NC=CC=C1COC1=CC=CC(O)=C1C=O FWCVZAQENIZVMY-UHFFFAOYSA-N 0.000 claims 8
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 8
- 150000002431 hydrogen Chemical class 0.000 claims 7
- 125000003118 aryl group Chemical group 0.000 claims 6
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 229910052799 carbon Inorganic materials 0.000 claims 3
- 229910052760 oxygen Inorganic materials 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- LAFDCOJCHVMHEK-UHFFFAOYSA-N 3-formyl-4-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzonitrile Chemical compound O=CC1=CC(C#N)=CC=C1OCC1=CC=CN2C1=NC=C2 LAFDCOJCHVMHEK-UHFFFAOYSA-N 0.000 claims 2
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 2
- KRGGDHHVSYRSIR-UHFFFAOYSA-N 5-methoxy-2-(1h-pyrrolo[2,3-b]pyridin-4-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=NC2=C1C=CN2 KRGGDHHVSYRSIR-UHFFFAOYSA-N 0.000 claims 2
- XNLXMKUOZPVVAY-UHFFFAOYSA-N 5-methoxy-2-(pyrrolo[1,2-a]pyrazin-6-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=C2N1C=CN=C2 XNLXMKUOZPVVAY-UHFFFAOYSA-N 0.000 claims 2
- 206010001052 Acute respiratory distress syndrome Diseases 0.000 claims 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims 2
- 208000013616 Respiratory Distress Syndrome Diseases 0.000 claims 2
- 201000000028 adult respiratory distress syndrome Diseases 0.000 claims 2
- 150000001299 aldehydes Chemical group 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 208000007056 sickle cell anemia Diseases 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- OYRNMRHRANZAEA-UHFFFAOYSA-N 2-(1h-indazol-4-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=C1C=NN2 OYRNMRHRANZAEA-UHFFFAOYSA-N 0.000 claims 1
- SXHIWHCDGVVVIB-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-3-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN=C2N1C=CC=C2 SXHIWHCDGVVVIB-UHFFFAOYSA-N 0.000 claims 1
- HITDPUASURIIIM-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-5-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=NC=CN12 HITDPUASURIIIM-UHFFFAOYSA-N 0.000 claims 1
- QHLPHLHHFIJUTA-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-6-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN2C=CN=C2C=C1 QHLPHLHHFIJUTA-UHFFFAOYSA-N 0.000 claims 1
- BOVHKSDADHYZQJ-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-7-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC2=NC=CN2C=C1 BOVHKSDADHYZQJ-UHFFFAOYSA-N 0.000 claims 1
- XJOOEFTYEAKFPQ-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-3-methoxybenzaldehyde Chemical compound COC1=CC=CC(C=O)=C1OCC1=CC=CN2C1=NC=C2 XJOOEFTYEAKFPQ-UHFFFAOYSA-N 0.000 claims 1
- IGCYNZLPHDJAFF-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OCC=2C3=NC=CN3C=CC=2)=C1 IGCYNZLPHDJAFF-UHFFFAOYSA-N 0.000 claims 1
- AJERFTOKIJSSNV-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CN2C1=NC=C2 AJERFTOKIJSSNV-UHFFFAOYSA-N 0.000 claims 1
- JIPTXLQISRYEFG-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)-5-methylbenzaldehyde Chemical compound O=CC1=CC(C)=CC=C1OCC1=CC=CN2C1=NC=C2 JIPTXLQISRYEFG-UHFFFAOYSA-N 0.000 claims 1
- DQAWRCYLXLPFGX-UHFFFAOYSA-N 2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC=CC=C1OCC1=CC=CN2C1=NC=C2 DQAWRCYLXLPFGX-UHFFFAOYSA-N 0.000 claims 1
- CXANJHAMRLLDTK-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-5-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=CN=CN12 CXANJHAMRLLDTK-UHFFFAOYSA-N 0.000 claims 1
- FKALBRNKMNOVHC-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-6-ylmethoxy)-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OCC2=CN3C=NC=C3C=C2)=C1 FKALBRNKMNOVHC-UHFFFAOYSA-N 0.000 claims 1
- QDLUTGMUCKWBAN-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-6-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN2C=NC=C2C=C1 QDLUTGMUCKWBAN-UHFFFAOYSA-N 0.000 claims 1
- OBVSYIPVNMKXQV-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-8-ylmethoxy)-4-methoxybenzaldehyde Chemical compound COC1=CC=C(C=O)C(OCC=2C3=CN=CN3C=CC=2)=C1 OBVSYIPVNMKXQV-UHFFFAOYSA-N 0.000 claims 1
- VKOMJTJRYAGKIV-UHFFFAOYSA-N 2-(imidazo[1,5-a]pyridin-8-ylmethoxy)-5-methoxybenzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CN2C1=CN=C2 VKOMJTJRYAGKIV-UHFFFAOYSA-N 0.000 claims 1
- RVRQTALZXUANFL-UHFFFAOYSA-N 2-[(1-methylimidazol-2-yl)methoxy]benzaldehyde Chemical compound CN1C=CN=C1COC1=CC=CC=C1C=O RVRQTALZXUANFL-UHFFFAOYSA-N 0.000 claims 1
- QNMDAKAPCVVQQP-UHFFFAOYSA-N 2-[(2-nitropyridin-3-yl)oxymethyl]benzene-1,3-dicarbaldehyde Chemical compound [O-][N+](=O)C1=NC=CC=C1OCC1=C(C=O)C=CC=C1C=O QNMDAKAPCVVQQP-UHFFFAOYSA-N 0.000 claims 1
- INLKHRAYLFROSM-UHFFFAOYSA-N 2-[(7-chloroquinolin-2-yl)methoxy]-5-nitrobenzaldehyde Chemical compound O=CC1=CC([N+](=O)[O-])=CC=C1OCC1=CC=C(C=CC(Cl)=C2)C2=N1 INLKHRAYLFROSM-UHFFFAOYSA-N 0.000 claims 1
- WEWBVBKSBQBVFI-UHFFFAOYSA-N 2-[(7-chloroquinolin-2-yl)methoxy]benzene-1,3-dicarbaldehyde Chemical compound N=1C2=CC(Cl)=CC=C2C=CC=1COC1=C(C=O)C=CC=C1C=O WEWBVBKSBQBVFI-UHFFFAOYSA-N 0.000 claims 1
- LJUWDMROBYYYNX-UHFFFAOYSA-N 2-[[1-[2-(2-methyl-5-nitroimidazol-1-yl)ethyl]triazol-4-yl]methoxy]benzaldehyde Chemical compound CC1=NC=C([N+]([O-])=O)N1CCN1N=NC(COC=2C(=CC=CC=2)C=O)=C1 LJUWDMROBYYYNX-UHFFFAOYSA-N 0.000 claims 1
- HYEMCPMRYDUHSN-UHFFFAOYSA-N 2-[[2-(4-tert-butyl-1,3-thiazol-2-yl)-1-benzofuran-5-yl]oxymethyl]benzaldehyde Chemical compound CC(C)(C)C1=CSC(C=2OC3=CC=C(OCC=4C(=CC=CC=4)C=O)C=C3C=2)=N1 HYEMCPMRYDUHSN-UHFFFAOYSA-N 0.000 claims 1
- GTAYSDREQLXNMN-UHFFFAOYSA-N 2-fluoro-6-[[2-(2-propan-2-ylpyrazol-3-yl)pyridin-3-yl]methoxy]benzaldehyde Chemical compound CC(C)N1N=CC=C1C1=NC=CC=C1COC1=CC=CC(F)=C1C=O GTAYSDREQLXNMN-UHFFFAOYSA-N 0.000 claims 1
- QZQXJMNHOPSYBC-UHFFFAOYSA-N 2-fluoro-6-[[2-[2-(2,2,2-trifluoroethyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound FC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CC(F)(F)F)=C1C=O QZQXJMNHOPSYBC-UHFFFAOYSA-N 0.000 claims 1
- LLNUXVXQOAESCE-UHFFFAOYSA-N 2-fluoro-6-[[2-[2-(3,3,3-trifluoropropyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound FC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CCC(F)(F)F)=C1C=O LLNUXVXQOAESCE-UHFFFAOYSA-N 0.000 claims 1
- BUSDPAIYNWOKOG-UHFFFAOYSA-N 2-hydroxy-6-[[2-[2-(2,2,2-trifluoroethyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound OC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CC(F)(F)F)=C1C=O BUSDPAIYNWOKOG-UHFFFAOYSA-N 0.000 claims 1
- VPPVYRNEOIHMAM-UHFFFAOYSA-N 2-hydroxy-6-[[2-[2-(3,3,3-trifluoropropyl)pyrazol-3-yl]pyridin-3-yl]methoxy]benzaldehyde Chemical compound OC1=CC=CC(OCC=2C(=NC=CC=2)C=2N(N=CC=2)CCC(F)(F)F)=C1C=O VPPVYRNEOIHMAM-UHFFFAOYSA-N 0.000 claims 1
- RCLXRECDHREUJS-UHFFFAOYSA-N 3-(imidazo[1,2-a]pyridin-8-ylmethyl)-1,3-dihydro-2-benzofuran-1-ol Chemical compound C12=CC=CC=C2C(O)OC1CC1=CC=CN2C1=NC=C2 RCLXRECDHREUJS-UHFFFAOYSA-N 0.000 claims 1
- VWXGYOFEFGXHLR-UHFFFAOYSA-N 3-formyl-4-(imidazo[1,5-a]pyridin-5-ylmethoxy)benzonitrile Chemical compound O=CC1=CC(C#N)=CC=C1OCC1=CC=CC2=CN=CN12 VWXGYOFEFGXHLR-UHFFFAOYSA-N 0.000 claims 1
- PRYOWPXXQMPLLX-UHFFFAOYSA-N 3-methyl-2-[(2-nitropyridin-3-yl)oxymethyl]benzaldehyde Chemical compound CC1=CC=CC(C=O)=C1COC1=CC=CN=C1[N+]([O-])=O PRYOWPXXQMPLLX-UHFFFAOYSA-N 0.000 claims 1
- CIVJRNZQBJFPEY-UHFFFAOYSA-N 4-[(7-chloroquinolin-2-yl)methoxy]benzene-1,3-dicarbaldehyde Chemical compound N=1C2=CC(Cl)=CC=C2C=CC=1COC1=CC=C(C=O)C=C1C=O CIVJRNZQBJFPEY-UHFFFAOYSA-N 0.000 claims 1
- BERKGZQCMWOMFH-UHFFFAOYSA-N 4-chloro-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound ClC1=CC=C(C=O)C(OCC=2C3=NC=CN3C=CC=2)=C1 BERKGZQCMWOMFH-UHFFFAOYSA-N 0.000 claims 1
- BJRVCVXCUZTNOT-UHFFFAOYSA-N 4-fluoro-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound FC1=CC=C(C=O)C(OCC=2C3=NC=CN3C=CC=2)=C1 BJRVCVXCUZTNOT-UHFFFAOYSA-N 0.000 claims 1
- IOLJMWNHXRPCSE-UHFFFAOYSA-N 4-formyl-3-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzonitrile Chemical compound O=CC1=CC=C(C#N)C=C1OCC1=CC=CN2C1=NC=C2 IOLJMWNHXRPCSE-UHFFFAOYSA-N 0.000 claims 1
- QSPXWFLFNPDJTF-UHFFFAOYSA-N 5-bromo-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(Br)=CC=C1OCC1=CC=CN2C1=NC=C2 QSPXWFLFNPDJTF-UHFFFAOYSA-N 0.000 claims 1
- WCVNZCJUHMJOEH-UHFFFAOYSA-N 5-bromo-2-[(6-methylpyridin-3-yl)methoxy]benzaldehyde Chemical compound C1=NC(C)=CC=C1COC1=CC=C(Br)C=C1C=O WCVNZCJUHMJOEH-UHFFFAOYSA-N 0.000 claims 1
- MOHKJHQLXKCGPV-UHFFFAOYSA-N 5-ethyl-2-(imidazo[1,2-a]pyridin-8-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(CC)=CC=C1OCC1=CC=CN2C1=NC=C2 MOHKJHQLXKCGPV-UHFFFAOYSA-N 0.000 claims 1
- OAKLOYATUAFQQI-UHFFFAOYSA-N 5-methoxy-2-(1h-pyrazolo[3,4-b]pyridin-4-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=NC2=C1C=NN2 OAKLOYATUAFQQI-UHFFFAOYSA-N 0.000 claims 1
- ZGAQYTGICSHQIN-UHFFFAOYSA-N 5-methoxy-2-(pyrazolo[1,5-a]pyrazin-3-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=C2C=NC=CN2N=C1 ZGAQYTGICSHQIN-UHFFFAOYSA-N 0.000 claims 1
- NRGBAMJCLLKMCZ-UHFFFAOYSA-N 5-methoxy-2-(pyrrolo[1,2-a]pyrazin-4-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN=CC2=CC=CN12 NRGBAMJCLLKMCZ-UHFFFAOYSA-N 0.000 claims 1
- QHYINIBXOSBMIT-UHFFFAOYSA-N 5-methoxy-2-(quinolin-5-ylmethoxy)benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=NC=CC=C12 QHYINIBXOSBMIT-UHFFFAOYSA-N 0.000 claims 1
- PHGADRUHZNQNFN-UHFFFAOYSA-N 5-methoxy-2-[(1-methylindazol-4-yl)methoxy]benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CC2=C1C=NN2C PHGADRUHZNQNFN-UHFFFAOYSA-N 0.000 claims 1
- QSJNCVCFMKNDKW-UHFFFAOYSA-N 5-methoxy-2-[(8-methylimidazo[1,2-a]pyridin-2-yl)methoxy]benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CN(C=CC=C2C)C2=N1 QSJNCVCFMKNDKW-UHFFFAOYSA-N 0.000 claims 1
- OFTYDSFWKUUDNZ-UHFFFAOYSA-N 5-methoxy-2-[[2-(2-propan-2-ylpyrazol-3-yl)pyridin-3-yl]methoxy]benzaldehyde Chemical compound O=CC1=CC(OC)=CC=C1OCC1=CC=CN=C1C1=CC=NN1C(C)C OFTYDSFWKUUDNZ-UHFFFAOYSA-N 0.000 claims 1
- GLQWIOMIMKQPFA-UHFFFAOYSA-N 6-[(2-formyl-4-methoxyphenoxy)methyl]pyrrolo[1,2-a]pyrazine-7-carbonitrile Chemical compound O=CC1=CC(OC)=CC=C1OCC1=C(C#N)C=C2N1C=CN=C2 GLQWIOMIMKQPFA-UHFFFAOYSA-N 0.000 claims 1
- CWDLNRKREBPISR-UHFFFAOYSA-N 6-[(2-formyl-4-methoxyphenoxy)methyl]pyrrolo[1,2-a]pyrazine-7-carboxamide Chemical compound O=CC1=CC(OC)=CC=C1OCC1=C(C(N)=O)C=C2N1C=CN=C2 CWDLNRKREBPISR-UHFFFAOYSA-N 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- 206010011985 Decubitus ulcer Diseases 0.000 claims 1
- 206010021143 Hypoxia Diseases 0.000 claims 1
- 208000004852 Lung Injury Diseases 0.000 claims 1
- 208000019693 Lung disease Diseases 0.000 claims 1
- 206010028980 Neoplasm Diseases 0.000 claims 1
- 208000004210 Pressure Ulcer Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 206010069363 Traumatic lung injury Diseases 0.000 claims 1
- 208000025865 Ulcer Diseases 0.000 claims 1
- 206010052428 Wound Diseases 0.000 claims 1
- 208000027418 Wounds and injury Diseases 0.000 claims 1
- 208000008445 altitude sickness Diseases 0.000 claims 1
- 125000005214 aminoheteroaryl group Chemical group 0.000 claims 1
- 201000011510 cancer Diseases 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 150000004292 cyclic ethers Chemical class 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- 230000007954 hypoxia Effects 0.000 claims 1
- 231100000515 lung injury Toxicity 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- MEADIYLUVHACCV-UHFFFAOYSA-N n,n-diethyl-2-formyl-4-methoxy-3-(pyridin-4-ylmethoxy)benzamide Chemical compound CCN(CC)C(=O)C1=CC=C(OC)C(OCC=2C=CN=CC=2)=C1C=O MEADIYLUVHACCV-UHFFFAOYSA-N 0.000 claims 1
- KHPCVTBRFJFTGV-UHFFFAOYSA-N n-(2-formyl-4-methoxyphenyl)imidazo[1,2-a]pyridine-8-carboxamide Chemical compound O=CC1=CC(OC)=CC=C1NC(=O)C1=CC=CN2C1=NC=C2 KHPCVTBRFJFTGV-UHFFFAOYSA-N 0.000 claims 1
- RXFXGKDBNOKILL-UHFFFAOYSA-N n-(2-formylphenyl)imidazo[1,2-a]pyridine-8-carboxamide Chemical compound O=CC1=CC=CC=C1NC(=O)C1=CC=CN2C1=NC=C2 RXFXGKDBNOKILL-UHFFFAOYSA-N 0.000 claims 1
- BXNFZMDIMWCBHR-UHFFFAOYSA-N n-[6-[(2-formylphenoxy)methyl]pyridin-2-yl]acetamide Chemical compound CC(=O)NC1=CC=CC(COC=2C(=CC=CC=2)C=O)=N1 BXNFZMDIMWCBHR-UHFFFAOYSA-N 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- 125000004944 pyrazin-3-yl group Chemical group [H]C1=C([H])N=C(*)C([H])=N1 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 125000003831 tetrazolyl group Chemical group 0.000 claims 1
- DENPQNAWGQXKCU-UHFFFAOYSA-N thiophene-2-carboxamide Chemical compound NC(=O)C1=CC=CS1 DENPQNAWGQXKCU-UHFFFAOYSA-N 0.000 claims 1
- 230000000287 tissue oxygenation Effects 0.000 claims 1
- 231100000397 ulcer Toxicity 0.000 claims 1
- ATEDQANYWGMZND-UHFFFAOYSA-N CC(C)[n]1nccc1-c1c(CCl)cccn1 Chemical compound CC(C)[n]1nccc1-c1c(CCl)cccn1 ATEDQANYWGMZND-UHFFFAOYSA-N 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161581053P | 2011-12-28 | 2011-12-28 | |
| US61/581,053 | 2011-12-28 | ||
| US201261661320P | 2012-06-18 | 2012-06-18 | |
| US61/661,320 | 2012-06-18 | ||
| PCT/US2012/072177 WO2013102142A1 (en) | 2011-12-28 | 2012-12-28 | Substituted benzaldehyde compounds and methods for their use in increasing tissue oxygenation |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017077318A Division JP6424399B2 (ja) | 2011-12-28 | 2017-04-10 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015504061A JP2015504061A (ja) | 2015-02-05 |
| JP2015504061A5 true JP2015504061A5 (enExample) | 2016-07-28 |
| JP6242810B2 JP6242810B2 (ja) | 2017-12-06 |
Family
ID=48698669
Family Applications (7)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014550525A Active JP6242810B2 (ja) | 2011-12-28 | 2012-12-28 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
| JP2017077318A Active JP6424399B2 (ja) | 2011-12-28 | 2017-04-10 | 置換ベンズアルデヒド化合物および組織酸素化の増加におけるそれらの使用方法 |
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