JP2011506474A5 - - Google Patents
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- JP2011506474A5 JP2011506474A5 JP2010538183A JP2010538183A JP2011506474A5 JP 2011506474 A5 JP2011506474 A5 JP 2011506474A5 JP 2010538183 A JP2010538183 A JP 2010538183A JP 2010538183 A JP2010538183 A JP 2010538183A JP 2011506474 A5 JP2011506474 A5 JP 2011506474A5
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- compound
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- hydrogen
- Prior art date
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- 150000001875 compounds Chemical class 0.000 claims description 117
- -1 n- propyl Chemical group 0.000 claims description 57
- 239000001257 hydrogen Substances 0.000 claims description 44
- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 42
- 125000005842 heteroatom Chemical group 0.000 claims description 40
- 229910052760 oxygen Inorganic materials 0.000 claims description 38
- 229910052717 sulfur Chemical group 0.000 claims description 36
- 125000001931 aliphatic group Chemical group 0.000 claims description 35
- 229910052757 nitrogen Inorganic materials 0.000 claims description 30
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 28
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 28
- 239000001301 oxygen Chemical group 0.000 claims description 28
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 27
- 239000011593 sulfur Chemical group 0.000 claims description 26
- 125000005843 halogen group Chemical group 0.000 claims description 23
- 125000003118 aryl group Chemical group 0.000 claims description 20
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 19
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 18
- 229920006395 saturated elastomer Polymers 0.000 claims description 18
- 150000002431 hydrogen Chemical class 0.000 claims description 17
- 108010079245 Cystic Fibrosis Transmembrane Conductance Regulator Proteins 0.000 claims description 15
- 102000008371 intracellularly ATP-gated chloride channel activity proteins Human genes 0.000 claims description 15
- 125000002950 monocyclic group Chemical group 0.000 claims description 15
- 125000001424 substituent group Chemical group 0.000 claims description 15
- 125000002619 bicyclic group Chemical group 0.000 claims description 14
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 14
- 230000007812 deficiency Effects 0.000 claims description 13
- 102100026383 Vasopressin-neurophysin 2-copeptin Human genes 0.000 claims description 12
- 201000010064 diabetes insipidus Diseases 0.000 claims description 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 10
- 125000000623 heterocyclic group Chemical group 0.000 claims description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
- 230000000694 effects Effects 0.000 claims description 9
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
- 206010006474 Bronchopulmonary aspergillosis allergic Diseases 0.000 claims description 6
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 6
- 206010033645 Pancreatitis Diseases 0.000 claims description 6
- 208000006778 allergic bronchopulmonary aspergillosis Diseases 0.000 claims description 6
- 239000012472 biological sample Substances 0.000 claims description 6
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
- 239000012634 fragment Substances 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000001072 heteroaryl group Chemical group 0.000 claims description 5
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 4
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- LPCQBTAOTIZGAE-UHFFFAOYSA-N 2h-pyrimidine-1-carboxamide Chemical compound NC(=O)N1CN=CC=C1 LPCQBTAOTIZGAE-UHFFFAOYSA-N 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 4
- 125000004174 2-benzimidazolyl group Chemical group [H]N1C(*)=NC2=C([H])C([H])=C([H])C([H])=C12 0.000 claims description 3
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- 206010010356 Congenital anomaly Diseases 0.000 claims description 3
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- 208000008955 Mucolipidoses Diseases 0.000 claims description 3
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- 208000002678 Mucopolysaccharidoses Diseases 0.000 claims description 3
- 102100026784 Myelin proteolipid protein Human genes 0.000 claims description 3
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- 208000018737 Parkinson disease Diseases 0.000 claims description 3
- 208000017493 Pelizaeus-Merzbacher disease Diseases 0.000 claims description 3
- 208000000609 Pick Disease of the Brain Diseases 0.000 claims description 3
- 108091000054 Prion Proteins 0.000 claims description 3
- 201000005660 Protein C Deficiency Diseases 0.000 claims description 3
- 208000021386 Sjogren Syndrome Diseases 0.000 claims description 3
- 208000009415 Spinocerebellar Ataxias Diseases 0.000 claims description 3
- 206010045261 Type IIa hyperlipidaemia Diseases 0.000 claims description 3
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 3
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- 230000037444 atrophy Effects 0.000 claims description 3
- 201000004562 autosomal dominant cerebellar ataxia Diseases 0.000 claims description 3
- 230000002146 bilateral effect Effects 0.000 claims description 3
- 206010006451 bronchitis Diseases 0.000 claims description 3
- 208000007451 chronic bronchitis Diseases 0.000 claims description 3
- 206010012601 diabetes mellitus Diseases 0.000 claims description 3
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- 208000030172 endocrine system disease Diseases 0.000 claims description 3
- 201000001386 familial hypercholesterolemia Diseases 0.000 claims description 3
- 208000013746 hereditary thrombophilia due to congenital protein C deficiency Diseases 0.000 claims description 3
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims description 3
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- 150000002632 lipids Chemical class 0.000 claims description 3
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- 208000020460 mucolipidosis II alpha/beta Diseases 0.000 claims description 3
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- 208000000638 myeloperoxidase deficiency Diseases 0.000 claims description 3
- 230000004770 neurodegeneration Effects 0.000 claims description 3
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 3
- 108010040003 polyglutamine Proteins 0.000 claims description 3
- 229920000155 polyglutamine Polymers 0.000 claims description 3
- 201000002212 progressive supranuclear palsy Diseases 0.000 claims description 3
- 230000020978 protein processing Effects 0.000 claims description 3
- 201000009890 sinusitis Diseases 0.000 claims description 3
- 230000000391 smoking effect Effects 0.000 claims description 3
- 208000011580 syndromic disease Diseases 0.000 claims description 3
- 210000001177 vas deferen Anatomy 0.000 claims description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 2
- KLIDCXVFHGNTTM-UHFFFAOYSA-N 2,6-dimethoxyphenol Chemical group COC1=CC=CC(OC)=C1O KLIDCXVFHGNTTM-UHFFFAOYSA-N 0.000 claims description 2
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 2
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 2
- UKDZIHPXUOIUBE-UHFFFAOYSA-N 7-ethyl-4-oxo-n-[3-(trifluoromethyl)-1h-indol-6-yl]-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound C1=C2C(C(F)(F)F)=CNC2=CC(NC(=O)C2=CNC3=CC(=CN3C2=O)CC)=C1 UKDZIHPXUOIUBE-UHFFFAOYSA-N 0.000 claims description 2
- GNYIWDPHISZCAJ-UHFFFAOYSA-N 7-ethyl-4-oxo-n-[5-(trifluoromethyl)-1h-indol-6-yl]-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound O=C1N2C=C(CC)C=C2NC=C1C(=O)NC(C(=C1)C(F)(F)F)=CC2=C1C=CN2 GNYIWDPHISZCAJ-UHFFFAOYSA-N 0.000 claims description 2
- QQOPRXFMMROSKY-UHFFFAOYSA-N 7-ethyl-n-[2-fluoro-5-hydroxy-4-(1-methylcyclohexyl)phenyl]-4-oxo-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound O=C1N2C=C(CC)C=C2NC=C1C(=O)NC(C(=C1)F)=CC(O)=C1C1(C)CCCCC1 QQOPRXFMMROSKY-UHFFFAOYSA-N 0.000 claims description 2
- XGGKIJONYVCYPT-UHFFFAOYSA-N 7-methyl-4-oxo-n-[3-(trifluoromethyl)-1h-indol-6-yl]-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound C1=C2C(C(F)(F)F)=CNC2=CC(NC(=O)C2=CNC3=CC(=CN3C2=O)C)=C1 XGGKIJONYVCYPT-UHFFFAOYSA-N 0.000 claims description 2
- CXYUDDYJTJSZKY-UHFFFAOYSA-N C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C)=C1NC(=O)C1=CNC2=CC=NN2C1=O Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C)=C1NC(=O)C1=CNC2=CC=NN2C1=O CXYUDDYJTJSZKY-UHFFFAOYSA-N 0.000 claims description 2
- KSMKKIBZTDNPMQ-UHFFFAOYSA-N C=1C=C(NC(=O)C=2C(N3N=CC=C3NC=2)=O)C(C(F)(F)F)=CC=1N1CCCC1 Chemical compound C=1C=C(NC(=O)C=2C(N3N=CC=C3NC=2)=O)C(C(F)(F)F)=CC=1N1CCCC1 KSMKKIBZTDNPMQ-UHFFFAOYSA-N 0.000 claims description 2
- 208000015439 Lysosomal storage disease Diseases 0.000 claims description 2
- XCUAIINAJCDIPM-XVFCMESISA-N N(4)-hydroxycytidine Chemical compound O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1C(=O)NC(=NO)C=C1 XCUAIINAJCDIPM-XVFCMESISA-N 0.000 claims description 2
- RKHJVKTUNODYJJ-UHFFFAOYSA-N N1C2=CC=NN2C(=O)C(C(=O)NC2=CC=3NC=CC=3C=C2C(F)(F)F)=C1 Chemical compound N1C2=CC=NN2C(=O)C(C(=O)NC2=CC=3NC=CC=3C=C2C(F)(F)F)=C1 RKHJVKTUNODYJJ-UHFFFAOYSA-N 0.000 claims description 2
- AHVCYAYHVQQESC-UHFFFAOYSA-N N1C2=CC=NN2C(=O)C(C(=O)NC=2C=C3NC=C(C3=CC=2)C(C)(C)C)=C1 Chemical compound N1C2=CC=NN2C(=O)C(C(=O)NC=2C=C3NC=C(C3=CC=2)C(C)(C)C)=C1 AHVCYAYHVQQESC-UHFFFAOYSA-N 0.000 claims description 2
- 208000012902 Nervous system disease Diseases 0.000 claims description 2
- LSVRZDJINJEYOH-UHFFFAOYSA-N O=C1N2N=C(C)C=C2NC=C1C(=O)NC(C(=C1)C(C)(C)C)=CC2=C1C=CN2 Chemical compound O=C1N2N=C(C)C=C2NC=C1C(=O)NC(C(=C1)C(C)(C)C)=CC2=C1C=CN2 LSVRZDJINJEYOH-UHFFFAOYSA-N 0.000 claims description 2
- CJYHLFAIRHUFSG-UHFFFAOYSA-N O=C1N2N=C(C)C=C2NC=C1C(=O)NC1=CC(O)=C(C(C)(C)C)C=C1C(C)(C)C Chemical compound O=C1N2N=C(C)C=C2NC=C1C(=O)NC1=CC(O)=C(C(C)(C)C)C=C1C(C)(C)C CJYHLFAIRHUFSG-UHFFFAOYSA-N 0.000 claims description 2
- 208000024777 Prion disease Diseases 0.000 claims description 2
- 208000004622 abetalipoproteinemia Diseases 0.000 claims description 2
- 239000002671 adjuvant Substances 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
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- 239000004599 antimicrobial Substances 0.000 claims description 2
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
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- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 2
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- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000002883 imidazolyl group Chemical group 0.000 claims description 2
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- 125000001041 indolyl group Chemical group 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 229940066491 mucolytics Drugs 0.000 claims description 2
- KTEBEMMMLNIPHB-UHFFFAOYSA-N n-(2,4-ditert-butyl-5-hydroxyphenyl)-7-ethyl-4-oxo-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound O=C1N2C=C(CC)C=C2NC=C1C(=O)NC1=CC(O)=C(C(C)(C)C)C=C1C(C)(C)C KTEBEMMMLNIPHB-UHFFFAOYSA-N 0.000 claims description 2
- VXBPRKYNBFJTAB-UHFFFAOYSA-N n-(3-tert-butyl-1h-indol-6-yl)-7-ethyl-4-oxo-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound C1=C2C(C(C)(C)C)=CNC2=CC(NC(=O)C2=CNC3=CC(=CN3C2=O)CC)=C1 VXBPRKYNBFJTAB-UHFFFAOYSA-N 0.000 claims description 2
- QSGVSPNYFDSCOM-UHFFFAOYSA-N n-[2-fluoro-5-hydroxy-4-(1-methylcyclohexyl)phenyl]-7-methyl-4-oxo-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound O=C1N2C=C(C)C=C2NC=C1C(=O)NC(C(=C1)F)=CC(O)=C1C1(C)CCCCC1 QSGVSPNYFDSCOM-UHFFFAOYSA-N 0.000 claims description 2
- YFNMNJHCEMBBAU-UHFFFAOYSA-N n-[4-(3,3-dimethylpyrrolidin-1-yl)-2-(trifluoromethyl)phenyl]-7-methyl-4-oxo-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound O=C1N2C=C(C)C=C2NC=C1C(=O)NC(C(=C1)C(F)(F)F)=CC=C1N1CCC(C)(C)C1 YFNMNJHCEMBBAU-UHFFFAOYSA-N 0.000 claims description 2
- ICPUHOLYWHUUGE-UHFFFAOYSA-N n-[4-cyclopentyl-5-hydroxy-2-(trifluoromethyl)phenyl]-7-methyl-4-oxo-1h-pyrrolo[1,2-a]pyrimidine-3-carboxamide Chemical compound O=C1N2C=C(C)C=C2NC=C1C(=O)NC(C(=C1)C(F)(F)F)=CC(O)=C1C1CCCC1 ICPUHOLYWHUUGE-UHFFFAOYSA-N 0.000 claims description 2
- 230000001537 neural effect Effects 0.000 claims description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
- 235000015097 nutrients Nutrition 0.000 claims description 2
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
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- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- HKSQZEGSMBFHGC-UHFFFAOYSA-N pyrimidine-4-carboxamide Chemical compound NC(=O)C1=CC=NC=N1 HKSQZEGSMBFHGC-UHFFFAOYSA-N 0.000 claims description 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 2
- 125000006413 ring segment Chemical group 0.000 claims description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000001113 thiadiazolyl group Chemical group 0.000 claims description 2
- 125000000335 thiazolyl group Chemical group 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 125000001425 triazolyl group Chemical group 0.000 claims description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims 2
- 125000003341 7 membered heterocyclic group Chemical group 0.000 claims 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims 1
- 208000013558 Developmental Bone disease Diseases 0.000 claims 1
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- 208000019715 inherited Creutzfeldt-Jakob disease Diseases 0.000 claims 1
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- 125000003107 substituted aryl group Chemical group 0.000 claims 1
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- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 description 2
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- 208000010859 Creutzfeldt-Jakob disease Diseases 0.000 description 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 2
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- 125000006217 methyl sulfide group Chemical group [H]C([H])([H])S* 0.000 description 2
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- 208000002320 spinal muscular atrophy Diseases 0.000 description 2
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 description 1
- DLNKGPWYATYSSQ-UHFFFAOYSA-N CN(C)[IH]c1cccc2c1cc[nH]2 Chemical compound CN(C)[IH]c1cccc2c1cc[nH]2 DLNKGPWYATYSSQ-UHFFFAOYSA-N 0.000 description 1
- HMMPHXCOTBASBC-UHFFFAOYSA-N Cc1ccc(cn[nH]2)c2c1 Chemical compound Cc1ccc(cn[nH]2)c2c1 HMMPHXCOTBASBC-UHFFFAOYSA-N 0.000 description 1
- 208000017701 Endocrine disease Diseases 0.000 description 1
- 206010031243 Osteogenesis imperfecta Diseases 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 125000005362 aryl sulfone group Chemical group 0.000 description 1
- 210000004556 brain Anatomy 0.000 description 1
- 239000000168 bronchodilator agent Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 210000003591 cerebellar nuclei Anatomy 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
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- 201000001119 neuropathy Diseases 0.000 description 1
- 230000007823 neuropathy Effects 0.000 description 1
- 230000011164 ossification Effects 0.000 description 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 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1333607P | 2007-12-13 | 2007-12-13 | |
| US61/013,336 | 2007-12-13 | ||
| PCT/US2008/086562 WO2009076593A1 (en) | 2007-12-13 | 2008-12-12 | Modulators of cystic fibrosis transmembrane conductance regulator |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011506474A JP2011506474A (ja) | 2011-03-03 |
| JP2011506474A5 true JP2011506474A5 (https=) | 2013-02-07 |
| JP5637859B2 JP5637859B2 (ja) | 2014-12-10 |
Family
ID=40404952
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010538183A Active JP5637859B2 (ja) | 2007-12-13 | 2008-12-12 | 嚢胞性線維症膜コンダクタンスレギュレーターのモジュレーター |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US8552006B2 (https=) |
| EP (1) | EP2231671B1 (https=) |
| JP (1) | JP5637859B2 (https=) |
| CN (1) | CN101925603B (https=) |
| AU (1) | AU2008335031B2 (https=) |
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| US5420128A (en) | 1990-10-09 | 1995-05-30 | Otsuka Pharmaceutical Co., Ltd. | Pyrimidine derivatives, method of manufacturing the same, and androgen inhibitor |
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