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)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Biomedical Technology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (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 | |
| GBGB0709031.9A GB0709031D0 (en) | 2007-05-10 | 2007-05-10 | Pharmaceutical compounds |
| US60/917,191 | 2007-05-10 | ||
| GB0709031.9 | 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 (cg-RX-API-DMAC7.html) | 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 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2170849B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP5555620B2 (cg-RX-API-DMAC7.html) |
| CN (1) | CN101796038B (cg-RX-API-DMAC7.html) |
| GB (1) | GB0709031D0 (cg-RX-API-DMAC7.html) |
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| SMT201900081T1 (it) | 2013-03-06 | 2019-05-10 | Incyte Holdings Corp | Procedimenti e intermedi per produrre un inibitore di jak |
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| 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 |
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| AR113922A1 (es) | 2017-12-08 | 2020-07-01 | Incyte Corp | Terapia de combinación de dosis baja para el tratamiento de neoplasias mieloproliferativas |
| 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 |
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| BE794096A (fr) | 1972-08-07 | 1973-05-16 | Lepetit Spa | Oxazoles 2,4,5-trisubstitues et leur preparation |
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| 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 |
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| CN1267431C (zh) * | 2000-06-28 | 2006-08-02 | 阿斯特拉曾尼卡有限公司 | 取代的喹唑啉衍生物及其在制备作为抑制剂的药物中的用途 |
| PL205536B1 (pl) * | 2000-10-30 | 2010-04-30 | Janssen Pharmaceutica Nv | Podstawiona pochodna dihydroindolu, dihydrochinoliny lub dihydroizochinoliny jako inhibitor peptydazy tripeptydowej, jej zastosowanie i sposób wytwarzania oraz kompozycja farmaceutyczna |
| CA2491895C (en) * | 2002-07-09 | 2011-01-18 | Vertex Pharmaceuticals Incorporated | Inhibitors of c-jun n-terminal kinases (jnk) and other protein kinases |
| CA2532443A1 (en) * | 2003-07-24 | 2005-02-03 | Merck & Co., Inc. | Tyrosine kinase inhibitors |
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| GB0504753D0 (en) | 2005-03-08 | 2005-04-13 | Astrazeneca Ab | Chemical compounds |
| WO2007043401A1 (ja) | 2005-10-07 | 2007-04-19 | Kissei Pharmaceutical Co., Ltd. | 含窒素複素環化合物およびそれを含有する医薬組成物 |
| 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 |
| DE602007009085D1 (de) | 2006-05-12 | 2010-10-21 | Ab Science | Neues verfahren zur synthese von 2-aminooxazolverbindungen |
| US20090093452A1 (en) | 2006-08-24 | 2009-04-09 | Pfizer 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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| EP2170849B1 (en) | 2016-12-21 |
| US9187465B2 (en) | 2015-11-17 |
| JP2010526800A (ja) | 2010-08-05 |
| US8921544B2 (en) | 2014-12-30 |
| EP2170849A1 (en) | 2010-04-07 |
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