CA2746307C - Aminopyridine and carboxypyridine compounds as phosphodiesterase 10 inhibitors - Google Patents
Aminopyridine and carboxypyridine compounds as phosphodiesterase 10 inhibitors Download PDFInfo
- Publication number
- CA2746307C CA2746307C CA2746307A CA2746307A CA2746307C CA 2746307 C CA2746307 C CA 2746307C CA 2746307 A CA2746307 A CA 2746307A CA 2746307 A CA2746307 A CA 2746307A CA 2746307 C CA2746307 C CA 2746307C
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- CA
- Canada
- Prior art keywords
- pyridin
- compound
- pharmaceutically acceptable
- acceptable salt
- ylamino
- 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.)
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- 239000003112 inhibitor Substances 0.000 title description 30
- 108090001050 Phosphoric Diester Hydrolases Proteins 0.000 title description 9
- 102000004861 Phosphoric Diester Hydrolases Human genes 0.000 title description 7
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical class OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 title description 6
- 150000003927 aminopyridines Chemical class 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 709
- 150000003839 salts Chemical class 0.000 claims abstract description 491
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 56
- 201000010099 disease Diseases 0.000 claims abstract description 43
- 208000021384 Obsessive-Compulsive disease Diseases 0.000 claims abstract description 29
- 201000000980 schizophrenia Diseases 0.000 claims abstract description 24
- 208000020925 Bipolar disease Diseases 0.000 claims abstract description 18
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 153
- -1 5-quinolinyl Chemical group 0.000 claims description 127
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 107
- 229910052731 fluorine Inorganic materials 0.000 claims description 102
- 229920006395 saturated elastomer Polymers 0.000 claims description 102
- 229910052794 bromium Inorganic materials 0.000 claims description 101
- 229910052757 nitrogen Inorganic materials 0.000 claims description 88
- 229910052801 chlorine Inorganic materials 0.000 claims description 83
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 71
- 229910052739 hydrogen Inorganic materials 0.000 claims description 62
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 51
- ICSNLGPSRYBMBD-UHFFFAOYSA-N 2-aminopyridine Chemical compound NC1=CC=CC=N1 ICSNLGPSRYBMBD-UHFFFAOYSA-N 0.000 claims description 44
- 125000000623 heterocyclic group Chemical group 0.000 claims description 40
- 229910052799 carbon Inorganic materials 0.000 claims description 36
- 125000004429 atom Chemical group 0.000 claims description 35
- 125000005843 halogen group Chemical group 0.000 claims description 32
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 32
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims description 28
- 125000002950 monocyclic group Chemical group 0.000 claims description 28
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 26
- 125000001424 substituent group Chemical group 0.000 claims description 25
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 25
- 206010012289 Dementia Diseases 0.000 claims description 21
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 21
- 229910052717 sulfur Inorganic materials 0.000 claims description 20
- 125000002619 bicyclic group Chemical group 0.000 claims description 19
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 19
- 239000003814 drug Substances 0.000 claims description 18
- 229910052702 rhenium Inorganic materials 0.000 claims description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims description 16
- 208000036864 Attention deficit/hyperactivity disease Diseases 0.000 claims description 15
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 15
- 208000015802 attention deficit-hyperactivity disease Diseases 0.000 claims description 15
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 14
- 230000001898 pallidal effect Effects 0.000 claims description 14
- 239000011593 sulfur Substances 0.000 claims description 14
- 208000018737 Parkinson disease Diseases 0.000 claims description 13
- 208000028017 Psychotic disease Diseases 0.000 claims description 13
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 12
- 229910052740 iodine Inorganic materials 0.000 claims description 10
- 206010008748 Chorea Diseases 0.000 claims description 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
- 206010043118 Tardive Dyskinesia Diseases 0.000 claims description 8
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- 229910052760 oxygen Inorganic materials 0.000 claims description 7
- 125000003386 piperidinyl group Chemical group 0.000 claims description 7
- 210000002637 putamen Anatomy 0.000 claims description 7
- YTSQJSLXKWSKBB-UHFFFAOYSA-N 3-[2-[4-(pyridin-2-ylamino)phenoxy]pyridin-3-yl]cyclopentan-1-ol Chemical compound C1C(O)CCC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 YTSQJSLXKWSKBB-UHFFFAOYSA-N 0.000 claims description 6
- KZDALXNTKOJCBC-UHFFFAOYSA-N 3-fluoro-n-[4-[3-(oxan-4-yl)pyrazin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound FC1=CC=CN=C1NC(C=C1)=CC=C1OC1=NC=CN=C1C1CCOCC1 KZDALXNTKOJCBC-UHFFFAOYSA-N 0.000 claims description 6
- RDPSJUJEPIUILE-UHFFFAOYSA-N 5-methyl-n-[4-[3-(oxan-4-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound N1=CC(C)=CC=C1NC(C=C1)=CC=C1OC1=NC=CC=C1C1CCOCC1 RDPSJUJEPIUILE-UHFFFAOYSA-N 0.000 claims description 6
- COMCORKQVOAQLV-UHFFFAOYSA-N [4-(3-chloropyrazin-2-yl)oxyphenyl]-pyridin-2-ylmethanone Chemical compound ClC1=NC=CN=C1OC1=CC=C(C(=O)C=2N=CC=CC=2)C=C1 COMCORKQVOAQLV-UHFFFAOYSA-N 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 6
- JEKVYTJPEIHSFF-UHFFFAOYSA-N n-[4-(3-pyridin-4-ylpyridin-2-yl)oxyphenyl]pyridin-2-amine Chemical compound C=1C=CC=NC=1NC(C=C1)=CC=C1OC1=NC=CC=C1C1=CC=NC=C1 JEKVYTJPEIHSFF-UHFFFAOYSA-N 0.000 claims description 6
- MMPZKSPHWRDPHY-UHFFFAOYSA-N n-[4-[3-(2-methylpyridin-4-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound C1=NC(C)=CC(C=2C(=NC=CC=2)OC=2C=CC(NC=3N=CC=CC=3)=CC=2)=C1 MMPZKSPHWRDPHY-UHFFFAOYSA-N 0.000 claims description 6
- WKCXWIVGOHAMBX-UHFFFAOYSA-N n-[4-[3-(oxan-3-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound C1CCOCC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 WKCXWIVGOHAMBX-UHFFFAOYSA-N 0.000 claims description 6
- OUOCOSQUTDTFOI-UHFFFAOYSA-N n-[4-[3-(oxepan-4-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound C1CCOCCC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 OUOCOSQUTDTFOI-UHFFFAOYSA-N 0.000 claims description 6
- KZJDZHRONGUZNO-UHFFFAOYSA-N n-[4-[3-(oxolan-3-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound C1OCCC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 KZJDZHRONGUZNO-UHFFFAOYSA-N 0.000 claims description 6
- MBWWOZAOTCKLFQ-AEFFLSMTSA-N (1s,3r)-3-[2-[4-(pyridin-2-ylamino)phenoxy]pyridin-3-yl]cyclohexan-1-ol Chemical compound C1[C@@H](O)CCC[C@H]1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 MBWWOZAOTCKLFQ-AEFFLSMTSA-N 0.000 claims description 5
- QTQMKXPIYBIGSW-UHFFFAOYSA-N 1-[4-[3-[2-(pyridine-4-carbonyl)phenoxy]pyrazin-2-yl]piperazin-1-yl]ethanone Chemical compound C1CN(C(=O)C)CCN1C1=NC=CN=C1OC1=CC=CC=C1C(=O)C1=CC=NC=C1 QTQMKXPIYBIGSW-UHFFFAOYSA-N 0.000 claims description 5
- ZTJMEDZSQNWSAN-UHFFFAOYSA-N 3-methyl-n-[4-[3-(oxan-4-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound CC1=CC=CN=C1NC(C=C1)=CC=C1OC1=NC=CC=C1C1CCOCC1 ZTJMEDZSQNWSAN-UHFFFAOYSA-N 0.000 claims description 5
- DMIXVMKHTQBPGM-UHFFFAOYSA-N [4-[3-(2-methylpyridin-4-yl)pyrazin-2-yl]oxyphenyl]-pyridin-2-ylmethanone Chemical compound C1=NC(C)=CC(C=2C(=NC=CN=2)OC=2C=CC(=CC=2)C(=O)C=2N=CC=CC=2)=C1 DMIXVMKHTQBPGM-UHFFFAOYSA-N 0.000 claims description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
- 125000002757 morpholinyl group Chemical group 0.000 claims description 5
- NWENMUHTOLTNBS-UHFFFAOYSA-N n-[4-[3-(oxolan-2-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound C1CCOC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 NWENMUHTOLTNBS-UHFFFAOYSA-N 0.000 claims description 5
- 125000004193 piperazinyl group Chemical group 0.000 claims description 5
- UMTVKOCJSLGBPV-WBVHZDCISA-N (1s,3r)-3-[3-[4-(pyridin-2-ylamino)phenoxy]pyrazin-2-yl]cyclohexan-1-ol Chemical compound C1[C@@H](O)CCC[C@H]1C1=NC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 UMTVKOCJSLGBPV-WBVHZDCISA-N 0.000 claims description 4
- UMTVKOCJSLGBPV-RDJZCZTQSA-N (1s,3s)-3-[3-[4-(pyridin-2-ylamino)phenoxy]pyrazin-2-yl]cyclohexan-1-ol Chemical compound C1[C@@H](O)CCC[C@@H]1C1=NC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 UMTVKOCJSLGBPV-RDJZCZTQSA-N 0.000 claims description 4
- NDRIFXXUELNCHH-UHFFFAOYSA-N 1-[3-[4-(pyridin-2-ylamino)phenoxy]pyrazin-2-yl]piperidine-4-carbonitrile Chemical compound C1CC(C#N)CCN1C1=NC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 NDRIFXXUELNCHH-UHFFFAOYSA-N 0.000 claims description 4
- VQDHXUDBUXSBEX-UHFFFAOYSA-N 1-methyl-3-[2-[4-(pyridin-2-ylamino)phenoxy]pyridin-3-yl]cyclopentan-1-ol Chemical compound C1C(C)(O)CCC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 VQDHXUDBUXSBEX-UHFFFAOYSA-N 0.000 claims description 4
- PMGLZVXKDHUYHB-UHFFFAOYSA-N 3,5-difluoro-n-[4-[3-(oxan-4-yl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound FC1=CC(F)=CN=C1NC(C=C1)=CC=C1OC1=NC=CC=C1C1CCOCC1 PMGLZVXKDHUYHB-UHFFFAOYSA-N 0.000 claims description 4
- GOTUFSIPQGIMRB-UHFFFAOYSA-N 3-[2-[4-(pyridin-2-ylamino)phenoxy]pyridin-3-yl]cyclopent-2-en-1-one Chemical compound O=C1CCC(C=2C(=NC=CC=2)OC=2C=CC(NC=3N=CC=CC=3)=CC=2)=C1 GOTUFSIPQGIMRB-UHFFFAOYSA-N 0.000 claims description 4
- HOSGJQOAQJHUCH-UHFFFAOYSA-N 4-[2-[4-(pyridin-2-ylamino)phenoxy]pyridin-3-yl]cyclohexan-1-one Chemical compound C1CC(=O)CCC1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 HOSGJQOAQJHUCH-UHFFFAOYSA-N 0.000 claims description 4
- IETBWTROZWYCIP-UHFFFAOYSA-N 6-methyl-n-[4-[3-(trifluoromethyl)pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound CC1=CC=CC(NC=2C=CC(OC=3C(=CC=CN=3)C(F)(F)F)=CC=2)=N1 IETBWTROZWYCIP-UHFFFAOYSA-N 0.000 claims description 4
- 208000012601 choreatic disease Diseases 0.000 claims description 4
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- QBHHPAVYYCLELV-UHFFFAOYSA-N n-(cyclopropylmethyl)-2-[4-(pyridin-2-ylamino)phenoxy]pyridine-3-carboxamide Chemical compound C=1C=CN=C(OC=2C=CC(NC=3N=CC=CC=3)=CC=2)C=1C(=O)NCC1CC1 QBHHPAVYYCLELV-UHFFFAOYSA-N 0.000 claims description 4
- DNRPLFPGAXZDLB-UHFFFAOYSA-N n-[2-(1h-imidazol-5-yl)ethyl]-2-[4-(pyridin-2-ylamino)phenoxy]pyridine-3-carboxamide Chemical compound C=1C=CN=C(OC=2C=CC(NC=3N=CC=CC=3)=CC=2)C=1C(=O)NCCC1=CNC=N1 DNRPLFPGAXZDLB-UHFFFAOYSA-N 0.000 claims description 4
- KXQZFJHYULQDOX-UHFFFAOYSA-N n-[4-(3-benzylpyrazin-2-yl)oxyphenyl]pyridin-2-amine Chemical compound N=1C=CN=C(OC=2C=CC(NC=3N=CC=CC=3)=CC=2)C=1CC1=CC=CC=C1 KXQZFJHYULQDOX-UHFFFAOYSA-N 0.000 claims description 4
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- NEEOPVSYKMVPEJ-UHFFFAOYSA-N n-[4-[3-[2-(trifluoromethyl)pyridin-4-yl]pyridin-2-yl]oxyphenyl]pyridin-2-amine Chemical compound C1=NC(C(F)(F)F)=CC(C=2C(=NC=CC=2)OC=2C=CC(NC=3N=CC=CC=3)=CC=2)=C1 NEEOPVSYKMVPEJ-UHFFFAOYSA-N 0.000 claims description 4
- MDOGBFIVLMTVER-UHFFFAOYSA-N n-methyl-2-[4-(pyridin-2-ylamino)phenoxy]pyridine-3-carboxamide Chemical compound CNC(=O)C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 MDOGBFIVLMTVER-UHFFFAOYSA-N 0.000 claims description 4
- 125000001624 naphthyl group Chemical group 0.000 claims description 4
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 4
- OOGYQLSCIDNKTJ-UHFFFAOYSA-N 3-[2-[4-(pyridin-2-ylamino)phenoxy]pyridin-3-yl]prop-2-yn-1-ol Chemical compound OCC#CC1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 OOGYQLSCIDNKTJ-UHFFFAOYSA-N 0.000 claims description 3
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- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims description 3
- 125000002433 cyclopentenyl group Chemical group C1(=CCCC1)* 0.000 claims description 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
- 125000004852 dihydrofuranyl group Chemical group O1C(CC=C1)* 0.000 claims description 3
- 125000005043 dihydropyranyl group Chemical group O1C(CCC=C1)* 0.000 claims description 3
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims description 3
- PXEVDDDOJWZTFR-UHFFFAOYSA-N n-[4-(3-pyrrolidin-1-ylpyridin-2-yl)oxyphenyl]pyridin-2-amine Chemical compound C1CCCN1C1=CC=CN=C1OC(C=C1)=CC=C1NC1=CC=CC=N1 PXEVDDDOJWZTFR-UHFFFAOYSA-N 0.000 claims description 3
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- GXPHKUHSUJUWKP-UHFFFAOYSA-N troglitazone Chemical compound C1CC=2C(C)=C(O)C(C)=C(C)C=2OC1(C)COC(C=C1)=CC=C1CC1SC(=O)NC1=O GXPHKUHSUJUWKP-UHFFFAOYSA-N 0.000 description 1
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- WRSWIWOVJBYZAW-UHFFFAOYSA-M zinc;methanidylbenzene;bromide Chemical compound Br[Zn+].[CH2-]C1=CC=CC=C1 WRSWIWOVJBYZAW-UHFFFAOYSA-M 0.000 description 1
Classifications
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
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- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
- C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
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- Animal Behavior & Ethology (AREA)
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- Public Health (AREA)
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- Neurology (AREA)
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- Hospice & Palliative Care (AREA)
- Dermatology (AREA)
- Pulmonology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13843408P | 2008-12-17 | 2008-12-17 | |
| US13844308P | 2008-12-17 | 2008-12-17 | |
| US61/138,434 | 2008-12-17 | ||
| US61/138,443 | 2008-12-17 | ||
| PCT/US2009/068330 WO2010077992A1 (en) | 2008-12-17 | 2009-12-16 | Aminopyridine and carboxypyridine compounds as phosphodiesterase 10 inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2746307A1 CA2746307A1 (en) | 2010-07-08 |
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| WO2011058766A1 (en) * | 2009-11-16 | 2011-05-19 | Raqualia Pharma Inc. | Aryl carboxamide derivatives as ttx-s blockers |
| US8470820B2 (en) * | 2010-01-22 | 2013-06-25 | Hoffman-La Roche Inc. | Nitrogen-containing heteroaryl derivatives |
| WO2012018909A1 (en) * | 2010-08-04 | 2012-02-09 | Takeda Pharmaceutical Company Limited | Fused heterocyclic compounds |
| CN103476757A (zh) | 2011-02-18 | 2013-12-25 | 阿勒根公司 | 作为磷酸二酯酶10(pde10a)的抑制剂的取代的6,7-二烷氧基-3-异喹啉醇衍生物 |
| EP2714041B1 (en) | 2011-05-24 | 2016-10-19 | Merck Sharp & Dohme Corp. | Aryloxymethyl cyclopropane derivatives as pde10 inhibitors |
| WO2013000924A1 (en) * | 2011-06-27 | 2013-01-03 | Janssen Pharmaceutica Nv | 1-ARYL-4-METHYL-[1,2,4]TRIAZOLO[4,3-a]QUINOXALINE DERIVATIVES |
| MX357241B (es) * | 2011-08-25 | 2018-06-29 | Merck Sharp & Dohme | Inhibidores de fosfodiesterasa 10 de pirimidina. |
| US8470884B2 (en) | 2011-11-09 | 2013-06-25 | Hoffmann-La Roche Inc. | Alkenyl naphthylacetic acids |
| WO2013148537A1 (en) * | 2012-03-29 | 2013-10-03 | Ning Xi | Substituted spirobicyclic compounds and methods of use |
| BR112014027181A2 (pt) | 2012-05-15 | 2017-06-27 | Novartis Ag | derivados de benzamida para a inibição da atividade de abl1, abl2 e bcr-abl1 |
| WO2014001314A1 (en) | 2012-06-26 | 2014-01-03 | Janssen Pharmaceutica Nv | Combinations comprising pde 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and pde 10 inhibitors for use in the treatment of neurological or metabolic disorders |
| WO2014071044A1 (en) | 2012-11-01 | 2014-05-08 | Allergan, Inc. | Substituted 6,7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (pde10a) |
| US9200016B2 (en) | 2013-12-05 | 2015-12-01 | Allergan, Inc. | Substituted 6, 7-dialkoxy-3-isoquinoline derivatives as inhibitors of phosphodiesterase 10 (PDE 10A) |
| WO2017047602A1 (ja) | 2015-09-18 | 2017-03-23 | 科研製薬株式会社 | ビアリール誘導体及びそれを含有する医薬 |
| CN114539273A (zh) | 2016-06-07 | 2022-05-27 | 北京加科思新药研发有限公司 | 可用作shp2抑制剂的新型杂环衍生物 |
| US10906905B2 (en) | 2016-10-14 | 2021-02-02 | Jiangsu Hengrui Medicine Co., Ltd. | Five-membered heteroaryl ring bridged ring derivative, preparation method therefor and medical use thereof |
| HRP20241239T1 (hr) | 2017-03-23 | 2024-12-06 | Jacobio Pharmaceuticals Co., Ltd. | Novi heterociklički derivati korisni kao shp2 inhibitori |
| ES2894128T3 (es) * | 2017-07-12 | 2022-02-11 | Bristol Myers Squibb Co | Inhibidores aminoheterocíclicos de cinco miembros y aminoheterocíclicos bicíclicos de 5,6 o 6,6 miembros de ROCK para el tratamiento de la insuficiencia cardíaca |
| CN108997230B (zh) * | 2018-07-26 | 2020-08-04 | 山东大学 | 具有基质金属蛋白酶抑制活性的喹喔啉衍生物及其制备方法和应用 |
| WO2020063760A1 (en) | 2018-09-26 | 2020-04-02 | Jacobio Pharmaceuticals Co., Ltd. | Novel heterocyclic derivatives useful as shp2 inhibitors |
| JP2023553699A (ja) | 2020-12-17 | 2023-12-25 | メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング | ヘテロ芳香族イソチオシアネート類 |
| TWI878871B (zh) * | 2022-05-09 | 2025-04-01 | 大陸商浙江同源康醫藥股份有限公司 | 多環類化合物及其用途 |
| WO2025024688A1 (en) * | 2023-07-25 | 2025-01-30 | The Regents Of The University Of California | Ire1alpha inhibitors and uses thereof |
| WO2025024681A1 (en) * | 2023-07-25 | 2025-01-30 | The Regents Of The University Of California | Ire1alpha inhibitors and uses thereof |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US4107288A (en) | 1974-09-18 | 1978-08-15 | Pharmaceutical Society Of Victoria | Injectable compositions, nanoparticles useful therein, and process of manufacturing same |
| US4198417A (en) | 1979-01-10 | 1980-04-15 | American Hoechst Corporation | Phenoxyphenylpiperidines |
| PT72878B (en) | 1980-04-24 | 1983-03-29 | Merck & Co Inc | Process for preparing mannich-base hydroxamic acid pro-drugs for the improved delivery of non-steroidal anti-inflammatory agents |
| US5145684A (en) | 1991-01-25 | 1992-09-08 | Sterling Drug Inc. | Surface modified drug nanoparticles |
| US6800651B2 (en) | 2000-02-03 | 2004-10-05 | Eli Lilly And Company | Potentiators of glutamate receptors |
| WO2001087845A2 (en) * | 2000-05-15 | 2001-11-22 | Fujisawa Pharmaceutical Co., Ltd. | N-containing heterocyclic compounds and their use as 5-ht antagonists |
| HRP20080262T3 (hr) | 2003-04-04 | 2009-04-30 | H. Lundbeck A/S | Derivati 4-(2-feniloksifenil)-piperidin ili -1,2,3,6 tetrahidropiridin kao inhibitori ponovne apsorpcije serotonina |
| US20070032404A1 (en) | 2003-07-31 | 2007-02-08 | Bayer Pharmaceuticals Corporation | Methods for treating diabetes and related disorders using pde10a inhibitors |
| CA2537141A1 (en) | 2003-09-02 | 2005-03-10 | Merck And Co., Inc. | Bipyridyl amines and ethers as modulators of metabotropic glutamate receptor-5 |
| EP1722789A2 (en) * | 2004-03-08 | 2006-11-22 | Amgen Inc. | Therapeutic modulation of ppar (gamma) activity |
| US20060019975A1 (en) | 2004-07-23 | 2006-01-26 | Pfizer Inc | Novel piperidyl derivatives of quinazoline and isoquinoline |
| NL2000397C2 (nl) | 2006-01-05 | 2007-10-30 | Pfizer Prod Inc | Bicyclische heteroarylverbindingen als PDE10 inhibitoren. |
| CA2637658C (en) | 2006-01-23 | 2012-07-17 | Amgen Inc. | Aurora kinase modulators and method of use |
| US7560551B2 (en) * | 2006-01-23 | 2009-07-14 | Amgen Inc. | Aurora kinase modulators and method of use |
| WO2007129183A2 (en) * | 2006-05-02 | 2007-11-15 | Pfizer Products Inc. | Bicyclic heteroaryl compounds as pde10 inhibitors |
| US20080090834A1 (en) * | 2006-07-06 | 2008-04-17 | Pfizer Inc | Selective azole pde10a inhibitor compounds |
| WO2008057280A1 (en) | 2006-10-27 | 2008-05-15 | Amgen Inc. | Multi-cyclic compounds and methods of use |
| WO2008079294A1 (en) | 2006-12-20 | 2008-07-03 | Amgen Inc. | Substituted heterocycles and methods of use |
| WO2009081259A1 (en) | 2007-12-21 | 2009-07-02 | Pfizer Inc. | Phenoxy-pyridyl derivatives |
| CN102203074A (zh) | 2008-06-20 | 2011-09-28 | 麦它波莱克斯股份有限公司 | 芳基gpr119激动剂及其用途 |
| TWI396689B (zh) * | 2008-11-14 | 2013-05-21 | Amgen Inc | 作為磷酸二酯酶10抑制劑之吡衍生物 |
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- 2009-12-16 ES ES09793422T patent/ES2397934T3/es active Active
- 2009-12-16 CA CA2746307A patent/CA2746307C/en not_active Expired - Fee Related
- 2009-12-16 WO PCT/US2009/068330 patent/WO2010077992A1/en not_active Ceased
- 2009-12-16 JP JP2011542411A patent/JP2012512255A/ja not_active Ceased
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- 2009-12-16 AU AU2009333214A patent/AU2009333214B2/en not_active Ceased
- 2009-12-17 TW TW098143428A patent/TW201035051A/zh unknown
- 2009-12-17 AR ARP090104944A patent/AR074775A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP2376455A1 (en) | 2011-10-19 |
| ES2397934T3 (es) | 2013-03-12 |
| US20100160280A1 (en) | 2010-06-24 |
| US8637500B2 (en) | 2014-01-28 |
| AU2009333214A1 (en) | 2011-06-30 |
| WO2010077992A1 (en) | 2010-07-08 |
| AR074775A1 (es) | 2011-02-09 |
| EP2376455B1 (en) | 2012-11-14 |
| CA2746307A1 (en) | 2010-07-08 |
| AU2009333214B2 (en) | 2013-09-26 |
| MX2011006575A (es) | 2011-10-06 |
| JP2012512255A (ja) | 2012-05-31 |
| TW201035051A (en) | 2010-10-01 |
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