JP5868521B2 - Ｒａｆキナーゼ阻害剤としての縮合三環式化合物 - Google Patents
Ｒａｆキナーゼ阻害剤としての縮合三環式化合物 Download PDFInfo
- Publication number
- JP5868521B2 JP5868521B2 JP2014549294A JP2014549294A JP5868521B2 JP 5868521 B2 JP5868521 B2 JP 5868521B2 JP 2014549294 A JP2014549294 A JP 2014549294A JP 2014549294 A JP2014549294 A JP 2014549294A JP 5868521 B2 JP5868521 B2 JP 5868521B2
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- JP
- Japan
- Prior art keywords
- heterocyclyl
- aryl
- heteroaryl
- alkyl
- cycloalkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 0 *c1c(*)c(*)c(*)c2c1[n]c(C1C3c4cc(Oc5ccnc(N6)c5CCC6=O)ccc4*C13)n2 Chemical compound *c1c(*)c(*)c(*)c2c1[n]c(C1C3c4cc(Oc5ccnc(N6)c5CCC6=O)ccc4*C13)n2 0.000 description 5
- IDPMEHVHCGDRQP-IJUHEHPCSA-N C/C=C(\C(COC(N1)=O)=C1N=C)/Oc(cc1C23)ccc1OC2C3c1nc2ccc(C(F)(F)F)cc2[nH]1 Chemical compound C/C=C(\C(COC(N1)=O)=C1N=C)/Oc(cc1C23)ccc1OC2C3c1nc2ccc(C(F)(F)F)cc2[nH]1 IDPMEHVHCGDRQP-IJUHEHPCSA-N 0.000 description 2
- ORICJDZBVSZLBO-UHFFFAOYSA-N FC(C1=CC2NC(C(C3c4c5)=C3Oc4ccc5Oc3ccnc4c3cc[nH]4)=NC2C=C1)(F)F Chemical compound FC(C1=CC2NC(C(C3c4c5)=C3Oc4ccc5Oc3ccnc4c3cc[nH]4)=NC2C=C1)(F)F ORICJDZBVSZLBO-UHFFFAOYSA-N 0.000 description 2
- GBKYUTIMIIUUJY-UHFFFAOYSA-N FC(c(cc1)cc2c1nc(C(C13)C1Oc(cc1)c3cc1Oc1ncncc1)[nH]2)(F)F Chemical compound FC(c(cc1)cc2c1nc(C(C13)C1Oc(cc1)c3cc1Oc1ncncc1)[nH]2)(F)F GBKYUTIMIIUUJY-UHFFFAOYSA-N 0.000 description 2
- WUKXLHCMACZFQG-UHFFFAOYSA-N FC(c1c[nH]c(-c2nccc(OCc(cc3C45)ccc3OC4C5c3nc(ccc(C(F)(F)F)c4)c4[nH]3)c2)n1)(F)F Chemical compound FC(c1c[nH]c(-c2nccc(OCc(cc3C45)ccc3OC4C5c3nc(ccc(C(F)(F)F)c4)c4[nH]3)c2)n1)(F)F WUKXLHCMACZFQG-UHFFFAOYSA-N 0.000 description 2
- RXIBRRYCPYLXQL-UHFFFAOYSA-N C=[Br]c1ccncc1 Chemical compound C=[Br]c1ccncc1 RXIBRRYCPYLXQL-UHFFFAOYSA-N 0.000 description 1
- XXPVTUVMTHAICX-UHFFFAOYSA-N CC(C)(C)OC(Nc1nccc(F)c1C=O)=O Chemical compound CC(C)(C)OC(Nc1nccc(F)c1C=O)=O XXPVTUVMTHAICX-UHFFFAOYSA-N 0.000 description 1
- PBFJMGJAQYCHKX-UHFFFAOYSA-N CCOC(C(C1c2c3)C1=Cc2ccc3OCc1ccccc1)O Chemical compound CCOC(C(C1c2c3)C1=Cc2ccc3OCc1ccccc1)O PBFJMGJAQYCHKX-UHFFFAOYSA-N 0.000 description 1
- NALCAYIRNHHHGC-UHFFFAOYSA-N CCOC(C(C1c2c3)C1Oc2ccc3O)=O Chemical compound CCOC(C(C1c2c3)C1Oc2ccc3O)=O NALCAYIRNHHHGC-UHFFFAOYSA-N 0.000 description 1
- QWHUFIZFVIZYHC-UHFFFAOYSA-N CCOC(C(C1c2c3)C1Oc2ccc3Oc1ccncc1)=O Chemical compound CCOC(C(C1c2c3)C1Oc2ccc3Oc1ccncc1)=O QWHUFIZFVIZYHC-UHFFFAOYSA-N 0.000 description 1
- VUZCEFIOTAPEKC-DNVJHFABSA-N Cc(c(F)c1)cc2c1nc([C@H]([C@H]1c3c4)[C@@H]1Oc3ccc4Oc1ccnc(N3)c1CCC3=O)[nH]2 Chemical compound Cc(c(F)c1)cc2c1nc([C@H]([C@H]1c3c4)[C@@H]1Oc3ccc4Oc1ccnc(N3)c1CCC3=O)[nH]2 VUZCEFIOTAPEKC-DNVJHFABSA-N 0.000 description 1
- VUZCEFIOTAPEKC-VABKMULXSA-N Cc(cc1[nH]c([C@@H]([C@@H]23)[C@H]2Oc(cc2)c3cc2Oc2ccnc(N3)c2CCC3=O)nc1c1)c1F Chemical compound Cc(cc1[nH]c([C@@H]([C@@H]23)[C@H]2Oc(cc2)c3cc2Oc2ccnc(N3)c2CCC3=O)nc1c1)c1F VUZCEFIOTAPEKC-VABKMULXSA-N 0.000 description 1
- ZRJJPKPJRBUPFH-UHFFFAOYSA-N FC(C1=CC2NC(C(C3c4c5)C3Oc4ccc5Oc3ccncc3)=NC2C=C1)(F)F Chemical compound FC(C1=CC2NC(C(C3c4c5)C3Oc4ccc5Oc3ccncc3)=NC2C=C1)(F)F ZRJJPKPJRBUPFH-UHFFFAOYSA-N 0.000 description 1
- MQIILRMBQJPTPO-UHFFFAOYSA-N FC(c(cc1)cc2c1nc(C(C13)C1Oc(cc1)c3cc1Oc1ccncc1)[nH]2)(F)F Chemical compound FC(c(cc1)cc2c1nc(C(C13)C1Oc(cc1)c3cc1Oc1ccncc1)[nH]2)(F)F MQIILRMBQJPTPO-UHFFFAOYSA-N 0.000 description 1
- FMOHMXQHGJZHAX-UHFFFAOYSA-N FC(c(cc1)cc2c1nc(C(C1c3c4)C1Oc3ccc4Oc1ccnc3c1cc[nH]3)[nH]2)(F)F Chemical compound FC(c(cc1)cc2c1nc(C(C1c3c4)C1Oc3ccc4Oc1ccnc3c1cc[nH]3)[nH]2)(F)F FMOHMXQHGJZHAX-UHFFFAOYSA-N 0.000 description 1
- RQWJHUJJBYMJMN-UHFFFAOYSA-N Nc(ccc(C(F)(F)F)c1)c1N Chemical compound Nc(ccc(C(F)(F)F)c1)c1N RQWJHUJJBYMJMN-UHFFFAOYSA-N 0.000 description 1
- NGFFVZQXSRKHBM-NHNZYLEHSA-N O=C(CC1)Nc2c1c(Oc(cc1)cc([C@H]34)c1O[C@@H]3C4c1nc(ccc(C(F)(F)F)c3)c3[nH]1)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc(cc1)cc([C@H]34)c1O[C@@H]3C4c1nc(ccc(C(F)(F)F)c3)c3[nH]1)ccn2 NGFFVZQXSRKHBM-NHNZYLEHSA-N 0.000 description 1
- IOSVSJJCVDYJHK-YPAWHYETSA-N O=C(CC1)Nc2c1c(Oc(cc1[C@@H]34)ccc1O[C@H]3[C@@H]4c([nH]c1c3)nc1cc(Cl)c3Cl)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc(cc1[C@@H]34)ccc1O[C@H]3[C@@H]4c([nH]c1c3)nc1cc(Cl)c3Cl)ccn2 IOSVSJJCVDYJHK-YPAWHYETSA-N 0.000 description 1
- NGFFVZQXSRKHBM-YPAWHYETSA-N O=C(CC1)Nc2c1c(Oc(cc1[C@@H]34)ccc1O[C@H]3[C@@H]4c1nc3ccc(C(F)(F)F)cc3[nH]1)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc(cc1[C@@H]34)ccc1O[C@H]3[C@@H]4c1nc3ccc(C(F)(F)F)cc3[nH]1)ccn2 NGFFVZQXSRKHBM-YPAWHYETSA-N 0.000 description 1
- IOSVSJJCVDYJHK-FKBYEOEOSA-N O=C(CC1)Nc2c1c(Oc(cc1[C@H]34)ccc1O[C@@H]3[C@H]4c1nc(cc(c(Cl)c3)Cl)c3[nH]1)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc(cc1[C@H]34)ccc1O[C@@H]3[C@H]4c1nc(cc(c(Cl)c3)Cl)c3[nH]1)ccn2 IOSVSJJCVDYJHK-FKBYEOEOSA-N 0.000 description 1
- CBEGWCPFZLRDSX-FKBYEOEOSA-N O=C(CC1)Nc2c1c(Oc(cc1[C@H]34)ccc1O[C@@H]3[C@H]4c1nc3cc(Cl)c(C(F)(F)F)cc3[nH]1)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc(cc1[C@H]34)ccc1O[C@@H]3[C@H]4c1nc3cc(Cl)c(C(F)(F)F)cc3[nH]1)ccn2 CBEGWCPFZLRDSX-FKBYEOEOSA-N 0.000 description 1
- RBKYGVBCBBPYMX-IRXMKASPSA-N O=C(CC1)Nc2c1c(Oc1ccc(C[C@@H]([C@H]34)C3c3nc(ccc(C(F)(F)F)c5)c5[nH]3)c4c1)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc1ccc(C[C@@H]([C@H]34)C3c3nc(ccc(C(F)(F)F)c5)c5[nH]3)c4c1)ccn2 RBKYGVBCBBPYMX-IRXMKASPSA-N 0.000 description 1
- RBKYGVBCBBPYMX-VSDWSMLSSA-N O=C(CC1)Nc2c1c(Oc1ccc(C[C@H]([C@@H]34)[C@@H]3c3nc(ccc(C(F)(F)F)c5)c5[nH]3)c4c1)ccn2 Chemical compound O=C(CC1)Nc2c1c(Oc1ccc(C[C@H]([C@@H]34)[C@@H]3c3nc(ccc(C(F)(F)F)c5)c5[nH]3)c4c1)ccn2 RBKYGVBCBBPYMX-VSDWSMLSSA-N 0.000 description 1
- RRPVPQBOJFSTMW-UHFFFAOYSA-N O=C(N1)OCc2c1nccc2F Chemical compound O=C(N1)OCc2c1nccc2F RRPVPQBOJFSTMW-UHFFFAOYSA-N 0.000 description 1
- FXFLXRRTJVDXJG-UHFFFAOYSA-N O=C(N1)OCc2c1nccc2Oc(cc1C23)ccc1OC2C3c1nc2ccc(C(F)(F)F)cc2[nH]1 Chemical compound O=C(N1)OCc2c1nccc2Oc(cc1C23)ccc1OC2C3c1nc2ccc(C(F)(F)F)cc2[nH]1 FXFLXRRTJVDXJG-UHFFFAOYSA-N 0.000 description 1
- BDIXZBYSDCLBID-UHFFFAOYSA-N OC(C(C12)C1OC1C2=CC(Oc2ccncc2)=CC1)=O Chemical compound OC(C(C12)C1OC1C2=CC(Oc2ccncc2)=CC1)=O BDIXZBYSDCLBID-UHFFFAOYSA-N 0.000 description 1
- DPHDBGDSCGXZEJ-HIFRSBDPSA-O [OH2+]c(c([C@@H](C1)[C@H]1c1nc2cc(Cl)c(C(F)(F)F)cc2[nH]1)c1)ccc1Oc1ccnc(N2)c1CCC2=O Chemical compound [OH2+]c(c([C@@H](C1)[C@H]1c1nc2cc(Cl)c(C(F)(F)F)cc2[nH]1)c1)ccc1Oc1ccnc(N2)c1CCC2=O DPHDBGDSCGXZEJ-HIFRSBDPSA-O 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5365—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
- A61K31/52—Purines, e.g. adenine
-
- 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D473/00—Heterocyclic compounds containing purine ring systems
- C07D473/26—Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
- C07D473/28—Oxygen atom
- C07D473/30—Oxygen atom attached in position 6, e.g. hypoxanthine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
- C07D519/02—Ergot alkaloids of the cyclic peptide type
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/CN2011/085146 WO2013097224A1 (en) | 2011-12-31 | 2011-12-31 | Fused tricyclic compounds as raf kinase inhibitors |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016000312A Division JP6175519B2 (ja) | 2016-01-04 | 2016-01-04 | Ｒａｆキナーゼ阻害剤としての縮合三環式化合物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2015506353A JP2015506353A (ja) | 2015-03-02 |
| JP5868521B2 true JP5868521B2 (ja) | 2016-02-24 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014549294A Active JP5868521B2 (ja) | 2011-12-31 | 2011-12-31 | Ｒａｆキナーゼ阻害剤としての縮合三環式化合物 |
Country Status (28)
| Country | Link |
|---|---|
| US (3) | US9273046B2 (enExample) |
| EP (2) | EP2797888B1 (enExample) |
| JP (1) | JP5868521B2 (enExample) |
| KR (1) | KR101713391B1 (enExample) |
| CN (1) | CN103596926B (enExample) |
| AU (1) | AU2011384857B2 (enExample) |
| BR (1) | BR112014013108B1 (enExample) |
| CA (1) | CA2856347C (enExample) |
| CY (1) | CY1118226T1 (enExample) |
| DK (1) | DK2797888T3 (enExample) |
| EA (1) | EA025597B1 (enExample) |
| ES (1) | ES2588775T3 (enExample) |
| HR (1) | HRP20160641T1 (enExample) |
| HU (1) | HUE029656T2 (enExample) |
| IL (1) | IL233364A (enExample) |
| IN (1) | IN2014DN06166A (enExample) |
| LT (1) | LT2797888T (enExample) |
| ME (1) | ME02529B (enExample) |
| MX (1) | MX352617B (enExample) |
| NZ (1) | NZ624068A (enExample) |
| PL (1) | PL2797888T3 (enExample) |
| PT (1) | PT2797888T (enExample) |
| RS (1) | RS55196B1 (enExample) |
| SG (1) | SG11201401725SA (enExample) |
| SI (1) | SI2797888T1 (enExample) |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2016523269A (ja) * | 2013-06-28 | 2016-08-08 | ベイジーン リミテッド | Ｒａｆキナ−ゼおよび／またはＲａｆキナ−ゼの二量体阻害剤としての縮合三環式ウレア系化合物 |
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| JP2016196446A (ja) * | 2016-01-04 | 2016-11-24 | ベイジーン リミテッド | Ｒａｆキナーゼ阻害剤としての縮合三環式化合物 |
| US11534431B2 (en) | 2016-07-05 | 2022-12-27 | Beigene Switzerland Gmbh | Combination of a PD-1 antagonist and a RAF inhibitor for treating cancer |
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