JP5555620B2 - オキサゾールチロシンキナーゼ阻害剤 - Google Patents
オキサゾールチロシンキナーゼ阻害剤 Download PDFInfo
- Publication number
- JP5555620B2 JP5555620B2 JP2010506999A JP2010506999A JP5555620B2 JP 5555620 B2 JP5555620 B2 JP 5555620B2 JP 2010506999 A JP2010506999 A JP 2010506999A JP 2010506999 A JP2010506999 A JP 2010506999A JP 5555620 B2 JP5555620 B2 JP 5555620B2
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- Prior art keywords
- optionally substituted
- group
- alkyl
- substituents
- phenyl
- Prior art date
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- 0 CC(C1CCC1)=NC(*(N)=O)=C[C@@](CC1)CC=C1Cl Chemical compound CC(C1CCC1)=NC(*(N)=O)=C[C@@](CC1)CC=C1Cl 0.000 description 7
- LNMHWGDOMOKNES-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCN1c(cc1)ccc1-c1c(C(O)=O)nc(Nc2c(C)cccc2)[o]1)=O Chemical compound CC(C)(C)OC(N(CC1)CCN1c(cc1)ccc1-c1c(C(O)=O)nc(Nc2c(C)cccc2)[o]1)=O LNMHWGDOMOKNES-UHFFFAOYSA-N 0.000 description 1
- GBOXNWBBWFMNBB-JAIQZWGSSA-N CC(C)(C)OC(N(CCC1)CC1/C=N\C(c(cc1)ccc1N)=O)=O Chemical compound CC(C)(C)OC(N(CCC1)CC1/C=N\C(c(cc1)ccc1N)=O)=O GBOXNWBBWFMNBB-JAIQZWGSSA-N 0.000 description 1
- HLPLRLFCSHYRPH-UHFFFAOYSA-N CC(C)(C)OC(N(CCC1)CCN1c(cc1)ccc1N)=O Chemical compound CC(C)(C)OC(N(CCC1)CCN1c(cc1)ccc1N)=O HLPLRLFCSHYRPH-UHFFFAOYSA-N 0.000 description 1
- WHDMKEXVHNLVIZ-UHFFFAOYSA-N CC(Nc(cc1)ccc1-c1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1)=O Chemical compound CC(Nc(cc1)ccc1-c1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1)=O WHDMKEXVHNLVIZ-UHFFFAOYSA-N 0.000 description 1
- DQXVFWZFYXOOCZ-UHFFFAOYSA-N CC1(C)OB(c(cc2)ccc2NCCN(C)C)OC1(C)C Chemical compound CC1(C)OB(c(cc2)ccc2NCCN(C)C)OC1(C)C DQXVFWZFYXOOCZ-UHFFFAOYSA-N 0.000 description 1
- ZYVBIOGIPPTFHD-UHFFFAOYSA-N CCC(CC=CC1)C1F Chemical compound CCC(CC=CC1)C1F ZYVBIOGIPPTFHD-UHFFFAOYSA-N 0.000 description 1
- CJRGIPVGMBHLDA-UHFFFAOYSA-N CCOC(c1c(-c(cc2)ccc2N(CC2)CCN2C(OC(C)(C)C)=O)[o]c(-c2c(cn[nH]3)c3ccc2)n1)=O Chemical compound CCOC(c1c(-c(cc2)ccc2N(CC2)CCN2C(OC(C)(C)C)=O)[o]c(-c2c(cn[nH]3)c3ccc2)n1)=O CJRGIPVGMBHLDA-UHFFFAOYSA-N 0.000 description 1
- BVOOGQOLDGZSRE-UHFFFAOYSA-N CCOC(c1c(-c(cc2)ccc2OC)[o]cn1)=O Chemical compound CCOC(c1c(-c(cc2)ccc2OC)[o]cn1)=O BVOOGQOLDGZSRE-UHFFFAOYSA-N 0.000 description 1
- GKZRBFYQXLVQCR-UHFFFAOYSA-N CN(C)CCNc(cc1)ccc1-c1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1 Chemical compound CN(C)CCNc(cc1)ccc1-c1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1 GKZRBFYQXLVQCR-UHFFFAOYSA-N 0.000 description 1
- BPSLYSHEZPYOAJ-UHFFFAOYSA-N CNC(N(CC1)CCN1c(cc1)ccc1Nc1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1)=O Chemical compound CNC(N(CC1)CCN1c(cc1)ccc1Nc1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1)=O BPSLYSHEZPYOAJ-UHFFFAOYSA-N 0.000 description 1
- AHMNDNNZRGRDKV-UHFFFAOYSA-N CNCCNC(c(cc1)ccc1Nc1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1)=O Chemical compound CNCCNC(c(cc1)ccc1Nc1c(C(N)=O)nc(-c(c(F)ccc2)c2F)[o]1)=O AHMNDNNZRGRDKV-UHFFFAOYSA-N 0.000 description 1
- FGNXJAOHVJBZPE-UHFFFAOYSA-N COc(cc1)ccc1-c1c(C(N)=O)nc(Nc(cc2)ccc2OC)[o]1 Chemical compound COc(cc1)ccc1-c1c(C(N)=O)nc(Nc(cc2)ccc2OC)[o]1 FGNXJAOHVJBZPE-UHFFFAOYSA-N 0.000 description 1
- SIGOCRQLHRQERB-UHFFFAOYSA-N COc1cc(Nc2c(C(N)=O)nc(-c(c(F)ccc3)c3F)[o]2)cc(OC)c1OC Chemical compound COc1cc(Nc2c(C(N)=O)nc(-c(c(F)ccc3)c3F)[o]2)cc(OC)c1OC SIGOCRQLHRQERB-UHFFFAOYSA-N 0.000 description 1
- LDCZEUOBVPKDEX-UHFFFAOYSA-N NC(c1c(-c(cc2)ccc2N2CCNCC2)[o]c(-c2ccccc2F)n1)=O Chemical compound NC(c1c(-c(cc2)ccc2N2CCNCC2)[o]c(-c2ccccc2F)n1)=O LDCZEUOBVPKDEX-UHFFFAOYSA-N 0.000 description 1
- QPBOGPMINLCPQV-UHFFFAOYSA-N NC(c1c(-c(cc2)ccc2OCCN2CCCCC2)[o]c(-c(c(F)ccc2)c2Cl)n1)=O Chemical compound NC(c1c(-c(cc2)ccc2OCCN2CCCCC2)[o]c(-c(c(F)ccc2)c2Cl)n1)=O QPBOGPMINLCPQV-UHFFFAOYSA-N 0.000 description 1
- DCBFUBYHYIEKRF-UHFFFAOYSA-N NC(c1c(-c(cc2)ccc2OCCN2CCCCC2)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(-c(cc2)ccc2OCCN2CCCCC2)[o]c(-c(c(F)ccc2)c2F)n1)=O DCBFUBYHYIEKRF-UHFFFAOYSA-N 0.000 description 1
- IRWJSNTTZHKHKT-UHFFFAOYSA-N NC(c1c(-c2ccc(CNC(c3ccc[s]3)=O)cc2)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(-c2ccc(CNC(c3ccc[s]3)=O)cc2)[o]c(-c(c(F)ccc2)c2F)n1)=O IRWJSNTTZHKHKT-UHFFFAOYSA-N 0.000 description 1
- FJSFCVTUDWUICD-UHFFFAOYSA-N NC(c1c(-c2ccc[s]2)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(-c2ccc[s]2)[o]c(-c(c(F)ccc2)c2F)n1)=O FJSFCVTUDWUICD-UHFFFAOYSA-N 0.000 description 1
- GABPUASFBHNGTK-UHFFFAOYSA-N NC(c1c(-c2cccnc2)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(-c2cccnc2)[o]c(-c(c(F)ccc2)c2F)n1)=O GABPUASFBHNGTK-UHFFFAOYSA-N 0.000 description 1
- ZYZTVXWKVWCEIP-UHFFFAOYSA-N NC(c1c(-c2ncccc2)nc(-c(c(F)ccc2)c2F)[nH]1)=O Chemical compound NC(c1c(-c2ncccc2)nc(-c(c(F)ccc2)c2F)[nH]1)=O ZYZTVXWKVWCEIP-UHFFFAOYSA-N 0.000 description 1
- ZSNUWAGLIRXETK-UHFFFAOYSA-N NC(c1c(Nc(cc2)ccc2-c2n[o]c(CO)c2)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(Nc(cc2)ccc2-c2n[o]c(CO)c2)[o]c(-c(c(F)ccc2)c2F)n1)=O ZSNUWAGLIRXETK-UHFFFAOYSA-N 0.000 description 1
- BNPQFYOHAYLZID-AWEZNQCLSA-N NC(c1c(Nc(cc2)ccc2C(N2[C@H](CO)CCC2)=O)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(Nc(cc2)ccc2C(N2[C@H](CO)CCC2)=O)[o]c(-c(c(F)ccc2)c2F)n1)=O BNPQFYOHAYLZID-AWEZNQCLSA-N 0.000 description 1
- LELIWIPWPFFQAG-UHFFFAOYSA-N NC(c1c(Nc(cc2)ccc2C(NCCO)=O)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(Nc(cc2)ccc2C(NCCO)=O)[o]c(-c(c(F)ccc2)c2F)n1)=O LELIWIPWPFFQAG-UHFFFAOYSA-N 0.000 description 1
- PQNIZMHLJSQWQK-UHFFFAOYSA-N NC(c1c(Nc(cc2)ccc2C(O)=O)[o]c(-c(c(F)ccc2)c2F)n1)=O Chemical compound NC(c1c(Nc(cc2)ccc2C(O)=O)[o]c(-c(c(F)ccc2)c2F)n1)=O PQNIZMHLJSQWQK-UHFFFAOYSA-N 0.000 description 1
- ZQWNHEWJDHNSTN-UHFFFAOYSA-N NCC1OCCN(Cc2cccc(-c3c(C(N)=O)nc(-c(c(F)ccc4)c4F)[o]3)c2)C1 Chemical compound NCC1OCCN(Cc2cccc(-c3c(C(N)=O)nc(-c(c(F)ccc4)c4F)[o]3)c2)C1 ZQWNHEWJDHNSTN-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members 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
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/30—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D263/34—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D263/48—Nitrogen atoms not forming part of a nitro radical
-
- 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
- C07D401/04—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing aromatic 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
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Pulmonology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US91719107P | 2007-05-10 | 2007-05-10 | |
| GB0709031.9 | 2007-05-10 | ||
| GBGB0709031.9A GB0709031D0 (en) | 2007-05-10 | 2007-05-10 | Pharmaceutical compounds |
| US60/917,191 | 2007-05-10 | ||
| US98727307P | 2007-11-12 | 2007-11-12 | |
| US60/987,273 | 2007-11-12 | ||
| PCT/GB2008/001612 WO2008139161A1 (en) | 2007-05-10 | 2008-05-09 | Oxazole tyrosine kinase inhibitors |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2010526800A JP2010526800A (ja) | 2010-08-05 |
| JP2010526800A5 JP2010526800A5 (enExample) | 2011-06-23 |
| JP5555620B2 true JP5555620B2 (ja) | 2014-07-23 |
Family
ID=38219198
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2010506999A Active JP5555620B2 (ja) | 2007-05-10 | 2008-05-09 | オキサゾールチロシンキナーゼ阻害剤 |
Country Status (6)
| Country | Link |
|---|---|
| US (4) | US8378095B2 (enExample) |
| EP (1) | EP2170849B1 (enExample) |
| JP (1) | JP5555620B2 (enExample) |
| CN (1) | CN101796038B (enExample) |
| GB (1) | GB0709031D0 (enExample) |
| WO (1) | WO2008139161A1 (enExample) |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DK3184526T3 (en) | 2005-12-13 | 2019-01-14 | Incyte Holdings Corp | PYRROLO [2,3-D] PYRIMIDINE DERIVATIVES AS A JANUS-KINASE INHIBITOR |
| GB0709031D0 (en) | 2007-05-10 | 2007-06-20 | Sareum Ltd | Pharmaceutical compounds |
| EP2740731B1 (en) | 2007-06-13 | 2016-03-23 | Incyte Holdings Corporation | Crystalline salts of the janus kinase inhibitor (r)-3-(4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl)-3-cyclopentylpropanenitrile |
| US9029411B2 (en) | 2008-01-25 | 2015-05-12 | Millennium Pharmaceuticals, Inc. | Thiophenes and uses thereof |
| JP2011527680A (ja) * | 2008-07-09 | 2011-11-04 | メルク・シャープ・エンド・ドーム・コーポレイション | Janusキナーゼの阻害剤 |
| GB0820819D0 (en) * | 2008-11-13 | 2008-12-24 | Sareum Ltd | Pharmaceutical compounds |
| EP2391619A1 (en) | 2009-01-30 | 2011-12-07 | Millennium Pharmaceuticals, Inc. | Heteroaryls and their use as pi3k inhibitors |
| US9090601B2 (en) | 2009-01-30 | 2015-07-28 | Millennium Pharmaceuticals, Inc. | Thiazole derivatives |
| US8796314B2 (en) | 2009-01-30 | 2014-08-05 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| WO2010102958A1 (en) | 2009-03-09 | 2010-09-16 | Glaxo Group Limited | 4-oxadiazol-2 -yl- indazoles as inhibitors of p13 kinases |
| WO2010127152A2 (en) * | 2009-04-29 | 2010-11-04 | Irm Llc | Compounds and compositions as microsomal prostaglandin e synthase-1 inhibitors |
| CA2759476C (en) | 2009-04-30 | 2018-10-09 | Julie Nicole Hamblin | Novel compounds |
| WO2010135621A1 (en) | 2009-05-22 | 2010-11-25 | Incyte Corporation | 3-[4-(7h-pyrrolo[2,3-d]pyrimidin-4-yl)-1h-pyrazol-1-yl]octane- or heptane-nitrile as jak inhibitors |
| ES2487542T3 (es) | 2009-05-22 | 2014-08-21 | Incyte Corporation | Derivados de N-(hetero)aril-pirrolidina de pirazol-4-il-pirrolo[2,3-d]pirimidinas y pirrol-3-il-pirrolo[2,3-d]pirimidinas como inhibidores de cinasas Janus |
| WO2011028685A1 (en) | 2009-09-01 | 2011-03-10 | Incyte Corporation | Heterocyclic derivatives of pyrazol-4-yl-pyrrolo[2,3-d]pyrimidines as janus kinase inhibitors |
| SMT201800137T1 (it) | 2010-03-10 | 2018-07-17 | Incyte Holdings Corp | Derivati di piperidin-4-il azetidina come inibitori di jak1 |
| PH12012502296B1 (en) | 2010-05-21 | 2017-10-06 | Incyte Holdings Corp | Topical formulation for a jak inhibitor |
| CA2801074A1 (en) | 2010-06-04 | 2011-12-08 | Albany Molecular Research, Inc. | Glycine transporter-1 inhibitors, methods of making them, and uses thereof |
| US8859768B2 (en) | 2010-08-11 | 2014-10-14 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| SG10201506238SA (en) | 2010-08-11 | 2015-09-29 | Millennium Pharm Inc | Heteroaryls And Uses Thereof |
| US9062038B2 (en) | 2010-08-11 | 2015-06-23 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| US9326987B2 (en) | 2010-09-08 | 2016-05-03 | Glaxo Group Limited | Indazole derivatives for use in the treatment of influenza virus infection |
| PE20141044A1 (es) | 2010-10-13 | 2014-09-07 | Millennium Pharm Inc | Heteroarilos y sus usos |
| SG190839A1 (en) | 2010-11-19 | 2013-07-31 | Incyte Corp | Cyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
| ES2536415T3 (es) | 2010-11-19 | 2015-05-25 | Incyte Corporation | Pirrolopiridinas y pirrolopirimidinas sustituidas heterocíclicas como inhibidores de JAK |
| EP2712290A4 (en) * | 2011-05-19 | 2014-11-19 | Univ Leland Stanford Junior | ANTIPROLIFERATIVE COMPOUNDS AND METHOD FOR THEIR USE |
| WO2012177606A1 (en) | 2011-06-20 | 2012-12-27 | Incyte Corporation | Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors |
| WO2013018733A1 (ja) | 2011-07-29 | 2013-02-07 | 富士フイルム株式会社 | 1,5-ナフチリジン誘導体又はその塩 |
| TW201313721A (zh) | 2011-08-18 | 2013-04-01 | Incyte Corp | 作為jak抑制劑之環己基氮雜環丁烷衍生物 |
| UA111854C2 (uk) | 2011-09-07 | 2016-06-24 | Інсайт Холдінгс Корпорейшн | Способи і проміжні сполуки для отримання інгібіторів jak |
| WO2013096642A1 (en) * | 2011-12-23 | 2013-06-27 | Millennium Pharmaceuticals, Inc. | Heteroaryls and uses thereof |
| GB201202027D0 (en) * | 2012-02-06 | 2012-03-21 | Sareum Ltd | Pharmaceutical compounds |
| PL2634185T3 (pl) * | 2012-03-02 | 2016-06-30 | Sareum Ltd | Inhibitory kinazy TYK2 |
| WO2013173720A1 (en) | 2012-05-18 | 2013-11-21 | Incyte Corporation | Piperidinylcyclobutyl substituted pyrrolopyridine and pyrrolopyrimidine derivatives as jak inhibitors |
| PE20151157A1 (es) | 2012-11-15 | 2015-08-19 | Incyte Corp | Formas de dosificacion de ruxolitinib de liberacion sostenida |
| LT3489239T (lt) | 2013-03-06 | 2022-03-10 | Incyte Holdings Corporation | Jak inhibitoriaus gamybos būdai ir tarpiniai junginiai |
| UA120499C2 (uk) | 2013-08-07 | 2019-12-26 | Інсайт Корпорейшн | Лікування захворювань із застосуванням лікарських форм з уповільненим вивільненням для інгібітора jak1 |
| KR102191084B1 (ko) * | 2013-09-03 | 2020-12-15 | 사름 리미티드 | 약제학적 화합물 |
| WO2015184305A1 (en) | 2014-05-30 | 2015-12-03 | Incyte Corporation | TREATMENT OF CHRONIC NEUTROPHILIC LEUKEMIA (CNL) AND ATYPICAL CHRONIC MYELOID LEUKEMIA (aCML) BY INHIBITORS OF JAK1 |
| US10000474B2 (en) | 2014-11-11 | 2018-06-19 | Musc Foundation For Research Development | Histone deacetylase inhibitors and uses thereof |
| ES2796276T3 (es) | 2015-02-05 | 2020-11-26 | Ab Science | Compuestos con actividad antitumoral |
| CN104974095B (zh) * | 2015-06-30 | 2017-09-15 | 浙江大学 | 2,4,5‑多取代咪唑类化合物及制备方法 |
| CN105601580B (zh) * | 2015-11-29 | 2017-11-14 | 陈玉玲 | 一种噁唑类医药中间体化合物的合成方法 |
| GB201617871D0 (en) | 2016-10-21 | 2016-12-07 | Sareum Limited | Pharmaceutical compounds |
| US11331313B2 (en) | 2017-05-22 | 2022-05-17 | Whitehead Institute For Biomedical Research | KCC2 expression enhancing compounds and uses thereof |
| WO2019113487A1 (en) | 2017-12-08 | 2019-06-13 | Incyte Corporation | Low dose combination therapy for treatment of myeloproliferative neoplasms |
| IL276302B2 (en) | 2018-01-30 | 2023-11-01 | Incyte Corp | Procedures for preparing [1-(3-fluoro-2-(trifluoromethyl(isonicotinyl}piperidine-4-one) |
| CN111683976B (zh) | 2018-02-05 | 2022-11-18 | 生物辐射实验室股份有限公司 | 具有阴离子交换-疏水混合模式配体的色谱树脂 |
| WO2019164996A1 (en) * | 2018-02-21 | 2019-08-29 | Southern Research Institute | 2-aminoaryl-5-aryloxazole analogs for the treatment of neurodegenerative diseases |
| SMT202400306T1 (it) | 2018-03-30 | 2024-09-16 | Incyte Corp | Trattamento dell'idrosadenite suppurativa utilizzando inibitori di jak. |
| WO2019222497A1 (en) | 2018-05-17 | 2019-11-21 | Southern Research Institute | 2,5-aryl-thiazole analogs for the treatment of neurodegenerative diseases |
| GB201816369D0 (en) | 2018-10-08 | 2018-11-28 | Sareum Ltd | Pharmaceutical compounds |
| MX2021013317A (es) | 2019-04-30 | 2022-01-18 | Celgene Corp | Terapias de combinacion que comprenden inhibidores de apremilast y tyk2. |
| GB202005114D0 (en) | 2020-04-07 | 2020-05-20 | Sareum Ltd | Crystalline Forms of a Pharmaceutical Compound |
| US11833155B2 (en) | 2020-06-03 | 2023-12-05 | Incyte Corporation | Combination therapy for treatment of myeloproliferative neoplasms |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE794096A (fr) | 1972-08-07 | 1973-05-16 | Lepetit Spa | Oxazoles 2,4,5-trisubstitues et leur preparation |
| JPS6155456A (ja) | 1984-08-24 | 1986-03-19 | Toyota Motor Corp | 車輌用自動変速機のアイドル運転時制御方法 |
| JPH0753716B2 (ja) | 1986-07-02 | 1995-06-07 | 吉富製薬株式会社 | イミダゾ−ルカルボキサミド誘導体 |
| JPH0770133B2 (ja) | 1986-12-19 | 1995-07-31 | 三菱電機株式会社 | ヘツド支持機構 |
| JPH06310767A (ja) | 1993-04-26 | 1994-11-04 | Nec Corp | 寒剤容器の断熱支持構造 |
| DE19653355A1 (de) | 1996-12-20 | 1998-06-25 | Dresden Arzneimittel | Neue, antikonvulsiv wirkende Aminoimidazole und Verfahren zu ihrer Herstellung |
| GB0003154D0 (en) | 2000-02-12 | 2000-04-05 | Astrazeneca Uk Ltd | Novel compounds |
| MXPA02011974A (es) * | 2000-06-28 | 2004-09-06 | Astrazeneca Ab | Derivados de quinazolina sustituidos y su uso como inhibidores. |
| CN100400040C (zh) * | 2000-10-30 | 2008-07-09 | 詹森药业有限公司 | 三肽酶抑制剂 |
| JP4570955B2 (ja) * | 2002-07-09 | 2010-10-27 | バーテクス ファーマスーティカルズ インコーポレイテッド | プロテインキナーゼ阻害活性を持つイミダゾール類 |
| CN1829507A (zh) * | 2003-07-24 | 2006-09-06 | 麦克公司 | 酪氨酸激酶抑制剂 |
| CA2542909C (en) * | 2003-10-23 | 2012-07-10 | Ab Science | 2-aminoaryloxazole compounds as tyrosine kinase inhibitors |
| GB0504753D0 (en) | 2005-03-08 | 2005-04-13 | Astrazeneca Ab | Chemical compounds |
| KR20080066938A (ko) | 2005-10-07 | 2008-07-17 | 깃세이 야쿠힌 고교 가부시키가이샤 | 질소 함유 복소환 화합물 및 그것을 함유하는 의약 조성물 |
| DK200600313A (da) | 2006-03-03 | 2006-03-13 | Novo Nordisk As | Treating type 2 diabetes or metabolic syndrome with an interleukin 1beta inhibitor or an interleukin 1beta synthesis or release inhibitor |
| ATE480525T1 (de) | 2006-05-12 | 2010-09-15 | Ab Science | Neues verfahren zur synthese von 2- aminooxazolverbindungen |
| WO2008024980A2 (en) | 2006-08-24 | 2008-02-28 | Serenex, Inc. | Pyrrole, thiophene, furan, imidazole, oxazole, and thiazole derivatives |
| GB0709031D0 (en) | 2007-05-10 | 2007-06-20 | Sareum Ltd | Pharmaceutical compounds |
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