JP2008503575A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2008503575A5 JP2008503575A5 JP2007518004A JP2007518004A JP2008503575A5 JP 2008503575 A5 JP2008503575 A5 JP 2008503575A5 JP 2007518004 A JP2007518004 A JP 2007518004A JP 2007518004 A JP2007518004 A JP 2007518004A JP 2008503575 A5 JP2008503575 A5 JP 2008503575A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- phenyl
- pyrrolo
- pyridine
- cycloalkyl
- 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
Links
- 125000000217 alkyl group Chemical group 0.000 claims 85
- 150000001875 compounds Chemical class 0.000 claims 30
- 229910052739 hydrogen Inorganic materials 0.000 claims 18
- 239000001257 hydrogen Substances 0.000 claims 18
- 125000001072 heteroaryl group Chemical group 0.000 claims 15
- 229910052760 oxygen Inorganic materials 0.000 claims 15
- 229910052717 sulfur Inorganic materials 0.000 claims 15
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 14
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 14
- 125000005842 heteroatom Chemical group 0.000 claims 14
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 13
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 13
- 125000000623 heterocyclic group Chemical group 0.000 claims 10
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 9
- 150000002431 hydrogen Chemical group 0.000 claims 9
- 125000002877 alkyl aryl group Chemical group 0.000 claims 8
- 125000005213 alkyl heteroaryl group Chemical group 0.000 claims 8
- 125000003118 aryl group Chemical group 0.000 claims 8
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- 208000010877 cognitive disease Diseases 0.000 claims 6
- 230000002265 prevention Effects 0.000 claims 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 6
- 206010012289 Dementia Diseases 0.000 claims 5
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 5
- 239000003814 drug Substances 0.000 claims 5
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims 5
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- 229920006395 saturated elastomer Polymers 0.000 claims 5
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 4
- 208000028698 Cognitive impairment Diseases 0.000 claims 3
- 201000011240 Frontotemporal dementia Diseases 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- 201000004384 Alopecia Diseases 0.000 claims 2
- 208000024827 Alzheimer disease Diseases 0.000 claims 2
- 102000001267 GSK3 Human genes 0.000 claims 2
- 108010014905 Glycogen Synthase Kinase 3 Proteins 0.000 claims 2
- -1 OR 13 Chemical group 0.000 claims 2
- 208000018737 Parkinson disease Diseases 0.000 claims 2
- 230000032683 aging Effects 0.000 claims 2
- 230000006999 cognitive decline Effects 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 208000035475 disorder Diseases 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 206010027175 memory impairment Diseases 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 239000012453 solvate Substances 0.000 claims 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 1
- JLQYPGHUYIISHY-UHFFFAOYSA-N 5-[4-(2-morpholin-4-ylethoxy)phenyl]-n-pyridin-3-yl-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C=1NC2=NC=C(C=3C=CC(OCCN4CCOCC4)=CC=3)C=C2C=1C(=O)NC1=CC=CN=C1 JLQYPGHUYIISHY-UHFFFAOYSA-N 0.000 claims 1
- MOPSEUHKLBOUBD-UHFFFAOYSA-N 5-[4-(4-methylpiperazin-1-yl)sulfonyl-3-(trifluoromethoxy)phenyl]-n-pyridin-3-yl-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1CN(C)CCN1S(=O)(=O)C1=CC=C(C=2C=C3C(C(=O)NC=4C=NC=CC=4)=CNC3=NC=2)C=C1OC(F)(F)F MOPSEUHKLBOUBD-UHFFFAOYSA-N 0.000 claims 1
- LAWGIDINEOJMHR-UHFFFAOYSA-N 5-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-(2-methylsulfonylphenyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1CN(C)CCN1S(=O)(=O)C1=CC=C(C=2C=C3C(C(=O)NC=4C(=CC=CC=4)S(C)(=O)=O)=CNC3=NC=2)C=C1 LAWGIDINEOJMHR-UHFFFAOYSA-N 0.000 claims 1
- CZKAYKXAZLJSJO-UHFFFAOYSA-N 5-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-n-pyridin-3-yl-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1CN(C)CCN1S(=O)(=O)C1=CC=C(C=2C=C3C(C(=O)NC=4C=NC=CC=4)=CNC3=NC=2)C=C1 CZKAYKXAZLJSJO-UHFFFAOYSA-N 0.000 claims 1
- DMFRLUSFAKKQHL-UHFFFAOYSA-N 5-[4-(morpholin-4-ylmethyl)phenyl]-n-(2-thiophen-2-ylethyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C=1NC2=NC=C(C=3C=CC(CN4CCOCC4)=CC=3)C=C2C=1C(=O)NCCC1=CC=CS1 DMFRLUSFAKKQHL-UHFFFAOYSA-N 0.000 claims 1
- OVQZOSHVSHCOTM-UHFFFAOYSA-N 5-[4-(morpholin-4-ylmethyl)phenyl]-n-pentyl-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCCCC)=CNC2=NC=C1C(C=C1)=CC=C1CN1CCOCC1 OVQZOSHVSHCOTM-UHFFFAOYSA-N 0.000 claims 1
- CBHFIEXHLUUFGN-UHFFFAOYSA-N 5-[4-(morpholine-4-carbonyl)phenyl]-n-(2-morpholin-4-ylethyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C=1NC2=NC=C(C=3C=CC(=CC=3)C(=O)N3CCOCC3)C=C2C=1C(=O)NCCN1CCOCC1 CBHFIEXHLUUFGN-UHFFFAOYSA-N 0.000 claims 1
- DFAATBVOJZNCNC-UHFFFAOYSA-N 5-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]-n-(2-methylsulfonylphenyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1CN(C)CCN1CC1=CC=C(C=2C=C3C(C(=O)NC=4C(=CC=CC=4)S(C)(=O)=O)=CNC3=NC=2)C=C1 DFAATBVOJZNCNC-UHFFFAOYSA-N 0.000 claims 1
- KNNMGWDEKLAPNM-UHFFFAOYSA-N 5-[4-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]-n-(2-morpholin-4-ylethyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1CN(C)CCN1CCOC1=CC=C(C=2C=C3C(C(=O)NCCN4CCOCC4)=CNC3=NC=2)C=C1 KNNMGWDEKLAPNM-UHFFFAOYSA-N 0.000 claims 1
- CZMPVAHLRSLYGY-UHFFFAOYSA-N 5-[4-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]-n-pyridin-3-yl-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1CN(C)CCN1CCOC1=CC=C(C=2C=C3C(C(=O)NC=4C=NC=CC=4)=CNC3=NC=2)C=C1 CZMPVAHLRSLYGY-UHFFFAOYSA-N 0.000 claims 1
- 208000000044 Amnesia Diseases 0.000 claims 1
- 208000031091 Amnestic disease Diseases 0.000 claims 1
- 208000020925 Bipolar disease Diseases 0.000 claims 1
- 208000011990 Corticobasal Degeneration Diseases 0.000 claims 1
- 208000032131 Diabetic Neuropathies Diseases 0.000 claims 1
- 201000010374 Down Syndrome Diseases 0.000 claims 1
- 206010019196 Head injury Diseases 0.000 claims 1
- 208000023105 Huntington disease Diseases 0.000 claims 1
- 208000009829 Lewy Body Disease Diseases 0.000 claims 1
- 201000002832 Lewy body dementia Diseases 0.000 claims 1
- 208000019022 Mood disease Diseases 0.000 claims 1
- 208000014060 Niemann-Pick disease Diseases 0.000 claims 1
- 206010034010 Parkinsonism Diseases 0.000 claims 1
- 208000000609 Pick Disease of the Brain Diseases 0.000 claims 1
- 208000006011 Stroke Diseases 0.000 claims 1
- 206010044688 Trisomy 21 Diseases 0.000 claims 1
- 206010067584 Type 1 diabetes mellitus Diseases 0.000 claims 1
- 201000004810 Vascular dementia Diseases 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 231100000360 alopecia Toxicity 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 230000006986 amnesia Effects 0.000 claims 1
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 1
- 201000002996 androgenic alopecia Diseases 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000002585 base Substances 0.000 claims 1
- 210000000988 bone and bone Anatomy 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 claims 1
- 230000001684 chronic effect Effects 0.000 claims 1
- 239000003433 contraceptive agent Substances 0.000 claims 1
- 230000002254 contraceptive effect Effects 0.000 claims 1
- 230000007423 decrease Effects 0.000 claims 1
- 208000017004 dementia pugilistica Diseases 0.000 claims 1
- 206010012601 diabetes mellitus Diseases 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 1
- 239000012458 free base Substances 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- JOGDOWSSXITRFY-UHFFFAOYSA-N methyl 5-(4-piperidin-1-ylsulfonylphenyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCCCC1 JOGDOWSSXITRFY-UHFFFAOYSA-N 0.000 claims 1
- VLJMSHQPVFKFNQ-UHFFFAOYSA-N methyl 5-[4-(2-morpholin-4-ylethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1OCCN1CCOCC1 VLJMSHQPVFKFNQ-UHFFFAOYSA-N 0.000 claims 1
- RKPTVBINMGGGER-UHFFFAOYSA-N methyl 5-[4-(4-methylpiperazin-1-yl)sulfonyl-3-(trifluoromethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1OC(F)(F)F)=CC=C1S(=O)(=O)N1CCN(C)CC1 RKPTVBINMGGGER-UHFFFAOYSA-N 0.000 claims 1
- ADPVVAWRYYOKPY-UHFFFAOYSA-N methyl 5-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCN(C)CC1 ADPVVAWRYYOKPY-UHFFFAOYSA-N 0.000 claims 1
- MDFGMUGWHGCMGJ-UHFFFAOYSA-N methyl 5-[4-(morpholin-4-ylmethyl)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1CN1CCOCC1 MDFGMUGWHGCMGJ-UHFFFAOYSA-N 0.000 claims 1
- KPZAJMHJJSYSIH-UHFFFAOYSA-N methyl 5-[4-(piperidin-1-ylmethyl)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1CN1CCCCC1 KPZAJMHJJSYSIH-UHFFFAOYSA-N 0.000 claims 1
- YIXPNXNGBUFBFA-UHFFFAOYSA-N methyl 5-[4-[(4-methylpiperazin-1-yl)methyl]phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1CN1CCN(C)CC1 YIXPNXNGBUFBFA-UHFFFAOYSA-N 0.000 claims 1
- SXLCEUHWLMKILH-UHFFFAOYSA-N methyl 5-[4-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxylate Chemical compound C1=C2C(C(=O)OC)=CNC2=NC=C1C(C=C1)=CC=C1OCCN1CCN(C)CC1 SXLCEUHWLMKILH-UHFFFAOYSA-N 0.000 claims 1
- PQIOSYKVBBWRRI-UHFFFAOYSA-N methylphosphonyl difluoride Chemical group CP(F)(F)=O PQIOSYKVBBWRRI-UHFFFAOYSA-N 0.000 claims 1
- 208000027061 mild cognitive impairment Diseases 0.000 claims 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 claims 1
- CIVGJWQASHLUIB-UHFFFAOYSA-N n-(2-methoxyethyl)-5-[4-(4-methylpiperazin-1-yl)sulfonyl-3-(trifluoromethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCOC)=CNC2=NC=C1C(C=C1OC(F)(F)F)=CC=C1S(=O)(=O)N1CCN(C)CC1 CIVGJWQASHLUIB-UHFFFAOYSA-N 0.000 claims 1
- QQHFMFZTTUYYTR-UHFFFAOYSA-N n-(2-methoxyethyl)-5-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCOC)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCN(C)CC1 QQHFMFZTTUYYTR-UHFFFAOYSA-N 0.000 claims 1
- DZVALETZZKJKHB-UHFFFAOYSA-N n-(2-methoxyethyl)-5-[4-(morpholin-4-ylmethyl)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCOC)=CNC2=NC=C1C(C=C1)=CC=C1CN1CCOCC1 DZVALETZZKJKHB-UHFFFAOYSA-N 0.000 claims 1
- HQUHZVGGORWCKS-UHFFFAOYSA-N n-(2-methoxyphenyl)-5-[4-(2-morpholin-4-ylethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.COC1=CC=CC=C1NC(=O)C1=CNC2=NC=C(C=3C=CC(OCCN4CCOCC4)=CC=3)C=C12 HQUHZVGGORWCKS-UHFFFAOYSA-N 0.000 claims 1
- JLIARJJCFWZYJF-UHFFFAOYSA-N n-(2-methylsulfonylethyl)-5-(4-piperidin-1-ylsulfonylphenyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCS(=O)(=O)C)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCCCC1 JLIARJJCFWZYJF-UHFFFAOYSA-N 0.000 claims 1
- GLJHFOBNGHWZKT-UHFFFAOYSA-N n-(2-morpholin-4-ylethyl)-5-(4-morpholin-4-ylphenyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C=1NC2=NC=C(C=3C=CC(=CC=3)N3CCOCC3)C=C2C=1C(=O)NCCN1CCOCC1 GLJHFOBNGHWZKT-UHFFFAOYSA-N 0.000 claims 1
- IGCLRWGJKMYGMQ-UHFFFAOYSA-N n-(2-morpholin-4-ylethyl)-5-[4-(pyrrolidine-1-carbonyl)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C=1NC2=NC=C(C=3C=CC(=CC=3)C(=O)N3CCCC3)C=C2C=1C(=O)NCCN1CCOCC1 IGCLRWGJKMYGMQ-UHFFFAOYSA-N 0.000 claims 1
- PKHIOSKRCXIXEL-UHFFFAOYSA-N n-(3-methoxyphenyl)-5-[4-(2-morpholin-4-ylethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.COC1=CC=CC(NC(=O)C=2C3=CC(=CN=C3NC=2)C=2C=CC(OCCN3CCOCC3)=CC=2)=C1 PKHIOSKRCXIXEL-UHFFFAOYSA-N 0.000 claims 1
- ZBBWWSOHXXECEN-UHFFFAOYSA-N n-(3-methoxypropyl)-5-[4-(2-morpholin-4-ylethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCCOC)=CNC2=NC=C1C(C=C1)=CC=C1OCCN1CCOCC1 ZBBWWSOHXXECEN-UHFFFAOYSA-N 0.000 claims 1
- AXTDIAFHYUBGBD-UHFFFAOYSA-N n-(3-methoxypropyl)-5-[4-(4-methylpiperazin-1-yl)sulfonyl-3-(trifluoromethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCCOC)=CNC2=NC=C1C(C=C1OC(F)(F)F)=CC=C1S(=O)(=O)N1CCN(C)CC1 AXTDIAFHYUBGBD-UHFFFAOYSA-N 0.000 claims 1
- WIHAPMOHNKDQSE-UHFFFAOYSA-N n-(3-methoxypropyl)-5-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCCOC)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCN(C)CC1 WIHAPMOHNKDQSE-UHFFFAOYSA-N 0.000 claims 1
- WQQDQYCMHVMYQE-UHFFFAOYSA-N n-(3-methoxypropyl)-5-[4-(piperidin-1-ylmethyl)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCCOC)=CNC2=NC=C1C(C=C1)=CC=C1CN1CCCCC1 WQQDQYCMHVMYQE-UHFFFAOYSA-N 0.000 claims 1
- AFWGUKWVTZFRSU-UHFFFAOYSA-N n-(3-methoxypropyl)-5-[4-[2-(4-methylpiperazin-1-yl)ethoxy]phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NCCCOC)=CNC2=NC=C1C(C=C1)=CC=C1OCCN1CCN(C)CC1 AFWGUKWVTZFRSU-UHFFFAOYSA-N 0.000 claims 1
- KVDXAKICNTWMQL-UHFFFAOYSA-N n-methyl-5-(4-piperidin-1-ylsulfonylphenyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NC)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCCCC1 KVDXAKICNTWMQL-UHFFFAOYSA-N 0.000 claims 1
- LBKRARXZMZIRGK-UHFFFAOYSA-N n-methyl-5-[4-(4-methylpiperazin-1-yl)sulfonyl-3-(trifluoromethoxy)phenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NC)=CNC2=NC=C1C(C=C1OC(F)(F)F)=CC=C1S(=O)(=O)N1CCN(C)CC1 LBKRARXZMZIRGK-UHFFFAOYSA-N 0.000 claims 1
- SMEMVHDJBVTJHC-UHFFFAOYSA-N n-methyl-5-[4-(4-methylpiperazin-1-yl)sulfonylphenyl]-1h-pyrrolo[2,3-b]pyridine-3-carboxamide;hydrochloride Chemical compound Cl.C1=C2C(C(=O)NC)=CNC2=NC=C1C(C=C1)=CC=C1S(=O)(=O)N1CCN(C)CC1 SMEMVHDJBVTJHC-UHFFFAOYSA-N 0.000 claims 1
- 210000005036 nerve Anatomy 0.000 claims 1
- 208000015122 neurodegenerative disease Diseases 0.000 claims 1
- 210000002682 neurofibrillary tangle Anatomy 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 125000004043 oxo group Chemical group O=* 0.000 claims 1
- 230000007170 pathology Effects 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 201000002212 progressive supranuclear palsy Diseases 0.000 claims 1
- 201000000980 schizophrenia Diseases 0.000 claims 1
- 208000011580 syndromic disease Diseases 0.000 claims 1
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0401655A SE0401655D0 (sv) | 2004-06-24 | 2004-06-24 | New compounds |
| PCT/SE2005/000955 WO2006001754A1 (en) | 2004-06-24 | 2005-06-20 | New derivatives of 5-aryl-1h-pyrrolo [2, 3b] pyridine-3-carboxamide or 5-aryl-1h-pyrrolo [2, 3b] pyridine-3-carboxylic acid |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008503575A JP2008503575A (ja) | 2008-02-07 |
| JP2008503575A5 true JP2008503575A5 (OSRAM) | 2008-07-31 |
Family
ID=32733685
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007518004A Pending JP2008503575A (ja) | 2004-06-24 | 2005-06-20 | ５−アリール−１ｈ−ピロロ［２，３ｂ］ピリジン−３−カルボキサミド又は５−アリール−１ｈ−ピロロ［２，３ｂ］ピリジン−３−カルボン酸の新規な誘導体 |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20090018130A1 (OSRAM) |
| EP (1) | EP1761530A1 (OSRAM) |
| JP (1) | JP2008503575A (OSRAM) |
| CN (1) | CN1972943A (OSRAM) |
| AR (1) | AR049650A1 (OSRAM) |
| SE (1) | SE0401655D0 (OSRAM) |
| TW (1) | TW200606164A (OSRAM) |
| UY (1) | UY28979A1 (OSRAM) |
| WO (1) | WO2006001754A1 (OSRAM) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004054634A1 (de) * | 2004-11-12 | 2006-05-18 | Schwarz Pharma Ag | Azaindolcarboxamide |
| WO2009017453A1 (en) * | 2007-07-30 | 2009-02-05 | Astrazeneca Ab | New therapeutic combination of an antipsychotic and a gsk3 inhibitor 958 |
| WO2009017455A1 (en) * | 2007-07-30 | 2009-02-05 | Astrazeneca Ab | A new combination of (a) an alpha-4-beta-2 -neuronal nicotinic agonist and (b) a gsk3 inhibitor |
| WO2009017454A1 (en) * | 2007-07-30 | 2009-02-05 | Astrazeneca Ab | New therapeutic combination of a gsk3 inhibitor and an a7-nicotinic agonist 960 |
| EP2706059A1 (en) | 2008-06-11 | 2014-03-12 | Genentech, Inc. | Diazacarbazoles and methods of use |
| US20110183938A1 (en) | 2009-12-16 | 2011-07-28 | Genentech, Inc. | 1,7-diazacarbazoles and methods of use |
| JP2013530180A (ja) | 2010-06-16 | 2013-07-25 | パーデュー、ファーマ、リミテッド、パートナーシップ | アリール置換インドールおよびその使用 |
| WO2016008966A1 (en) | 2014-07-17 | 2016-01-21 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for treating neuromuscular junction-related diseases |
| WO2016207366A1 (en) | 2015-06-26 | 2016-12-29 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of viral infections |
| GB201519573D0 (en) | 2015-11-05 | 2015-12-23 | King S College London | Combination |
| KR101746199B1 (ko) | 2016-07-04 | 2017-06-13 | 기초과학연구원 | 질소 함유 헤테로아릴 유도체 및 GSK3β 저해제로서의 이의 용도 |
| AU2019264078A1 (en) * | 2018-05-02 | 2020-12-17 | Jw Pharmaceutical Corporation | Novel heterocycle derivative |
| CN110041328A (zh) * | 2019-05-22 | 2019-07-23 | 南京合巨药业有限公司 | 一种5-氟-1H-吡咯并[2,3-b]吡啶-3-羧酸的制备方法 |
| US20240166596A1 (en) * | 2021-07-16 | 2024-05-23 | Aphiotx Inc. | Sulfamoyl benzene derivatives and uses thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0106586D0 (en) * | 2001-03-16 | 2001-05-09 | Smithkline Beecham Plc | Novel compounds |
| CA2480317A1 (en) * | 2002-03-28 | 2003-10-09 | Eisai Co., Ltd. | 7-azaindoles as inhibitors of c-jun n-terminal kinases for the treatment of neurodegenerative disorders |
-
2004
- 2004-06-24 SE SE0401655A patent/SE0401655D0/xx unknown
-
2005
- 2005-06-13 TW TW094119531A patent/TW200606164A/zh unknown
- 2005-06-17 AR ARP050102505A patent/AR049650A1/es unknown
- 2005-06-20 CN CNA200580021231XA patent/CN1972943A/zh active Pending
- 2005-06-20 WO PCT/SE2005/000955 patent/WO2006001754A1/en not_active Ceased
- 2005-06-20 US US11/571,183 patent/US20090018130A1/en not_active Abandoned
- 2005-06-20 EP EP05754098A patent/EP1761530A1/en not_active Withdrawn
- 2005-06-20 JP JP2007518004A patent/JP2008503575A/ja active Pending
- 2005-06-23 UY UY28979A patent/UY28979A1/es not_active Application Discontinuation
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| RU2336275C2 (ru) | Пиримидопроизводные, характеризующиеся антипролиферативной активностью, и фармацевтическая композиция | |
| JP2008503575A5 (OSRAM) | ||
| RU2435757C2 (ru) | Производные 3-циклил-2-(4-сульфамоилфенил)-n-циклилпропионамида, применимые для лечения нарушенной переносимости глюкозы и диабета | |
| SI2961736T1 (en) | Histone demethylase inhibitors | |
| RU2001121186A (ru) | Производные пиразолкарбоновой кислоты, их получение, содержащие их фармацевтические композиции | |
| JP4137159B2 (ja) | セロトニン及びノルアドレナリン再取り込み阻害薬としてのｎ−ピロリジン−３−イル−アミド誘導体 | |
| CA2515343A1 (en) | Antiparasitic terpene alkaloids | |
| JP2010531345A5 (OSRAM) | ||
| CA2568608A1 (en) | Six membered amino-amide derivatives as angiogenesis inhibitors | |
| RU2011116226A (ru) | Пиразолопиридиновые производные как ингибиторы надфн-оксидазы | |
| JP2005526814A5 (OSRAM) | ||
| RU2007108861A (ru) | Трифтометилзамещенные бензамиды в качестве ингибиторов киназ | |
| JP2020502092A5 (OSRAM) | ||
| CA2523261A1 (en) | Fused pyrimidine derivatives with crf activity | |
| JP2007519754A5 (OSRAM) | ||
| BR0317294A (pt) | Composto, formulação farmacêutica, uso de um composto, métodos de prevenção e/ou tratamento de condições associadas com a glicogênio sintase quinase-3 e de prevenção e/ou tratamento de doenças, e, uso dos intermediários | |
| JP2009526821A (ja) | 注意欠陥多動性障害治療用の新規な医薬組成物 | |
| MXPA04002338A (es) | Derivados de carbazol y su uso como antagonistas receptores del npy5. | |
| MX2014004254A (es) | Derivados de carbamato / urea que contienen anillos de piperidina y piperazina como inhibidores del receptor h3. | |
| RU2007130144A (ru) | Гетероциклические соединения в качестве антагонистов cccr2b | |
| JP2019537592A5 (OSRAM) | ||
| RU2009103300A (ru) | Производные 2-бензоилимидазопиридинов, их получение и их применение в терапии | |
| WO2008153325A1 (en) | Triazole derivatives having antifungal activity, method for the preparation thereof, and pharmaceutical composition comprising the same | |
| JP2004525183A5 (OSRAM) | ||
| RU2005122615A (ru) | Соединения n-(индолэтил)циклоамина |