JP5596023B2 - レセプターチロシンキナーゼのインヒビターとしてのイミダゾピリジン誘導体 - Google Patents
レセプターチロシンキナーゼのインヒビターとしてのイミダゾピリジン誘導体 Download PDFInfo
- Publication number
- JP5596023B2 JP5596023B2 JP2011512999A JP2011512999A JP5596023B2 JP 5596023 B2 JP5596023 B2 JP 5596023B2 JP 2011512999 A JP2011512999 A JP 2011512999A JP 2011512999 A JP2011512999 A JP 2011512999A JP 5596023 B2 JP5596023 B2 JP 5596023B2
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- Japan
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- alkyl
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- compound
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- 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.)
- Expired - Fee Related
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- 0 CC(C)(C)*(C)(C)OCC*(CC1)C(C2CC(*CC3)*3CC2)C1=C Chemical compound CC(C)(C)*(C)(C)OCC*(CC1)C(C2CC(*CC3)*3CC2)C1=C 0.000 description 12
- NGHRUBVFDAKWBC-UHFFFAOYSA-N Clc1cc2ncc[n]2cc1 Chemical compound Clc1cc2ncc[n]2cc1 NGHRUBVFDAKWBC-UHFFFAOYSA-N 0.000 description 3
- PTGHXWLASOUVCP-UHFFFAOYSA-N CC1(C)OB(c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)OC1(C)C Chemical compound CC1(C)OB(c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)OC1(C)C PTGHXWLASOUVCP-UHFFFAOYSA-N 0.000 description 2
- OXFRWJAGUOTHEH-UHFFFAOYSA-N Clc(cc[n]12)cc1ncc2I Chemical compound Clc(cc[n]12)cc1ncc2I OXFRWJAGUOTHEH-UHFFFAOYSA-N 0.000 description 2
- WVGCPEDBFHEHEZ-UHFFFAOYSA-N Brc1c[nH]nc1 Chemical compound Brc1c[nH]nc1 WVGCPEDBFHEHEZ-UHFFFAOYSA-N 0.000 description 1
- DUCXLVIAUPCYIC-UHFFFAOYSA-N Brc1c[n](C2COCC2)nc1 Chemical compound Brc1c[n](C2COCC2)nc1 DUCXLVIAUPCYIC-UHFFFAOYSA-N 0.000 description 1
- QZBPFIHCDADLCD-UHFFFAOYSA-N Brc1nnc(C2OCCC2)[s]1 Chemical compound Brc1nnc(C2OCCC2)[s]1 QZBPFIHCDADLCD-UHFFFAOYSA-N 0.000 description 1
- TUBDRYBPIYWLAM-UHFFFAOYSA-N CC(C)(C)OC(N(CC1)CCC1[n]1ncc(-c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)c1)=O Chemical compound CC(C)(C)OC(N(CC1)CCC1[n]1ncc(-c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)c1)=O TUBDRYBPIYWLAM-UHFFFAOYSA-N 0.000 description 1
- LXMNKEMWIPCPIJ-UHFFFAOYSA-N CC(C)(C)OC(NCCNc1nc(Cl)ncc1F)=O Chemical compound CC(C)(C)OC(NCCNc1nc(Cl)ncc1F)=O LXMNKEMWIPCPIJ-UHFFFAOYSA-N 0.000 description 1
- WXPLRSVMGRAIGW-UHFFFAOYSA-N CC(Nc1ncc[s]1)=O Chemical compound CC(Nc1ncc[s]1)=O WXPLRSVMGRAIGW-UHFFFAOYSA-N 0.000 description 1
- ZZHAKZUFNIDWIA-UHFFFAOYSA-N CC1(C)OB(c2cc3ncc[n]3cc2)OC1(C)C Chemical compound CC1(C)OB(c2cc3ncc[n]3cc2)OC1(C)C ZZHAKZUFNIDWIA-UHFFFAOYSA-N 0.000 description 1
- OEJWMHAIIQUWQR-UHFFFAOYSA-N CN(CCC1)CC1[n]1ncc(Br)c1 Chemical compound CN(CCC1)CC1[n]1ncc(Br)c1 OEJWMHAIIQUWQR-UHFFFAOYSA-N 0.000 description 1
- GCAGOMTVWIYPLE-UHFFFAOYSA-N CNc1ccc(-c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)nn1 Chemical compound CNc1ccc(-c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)nn1 GCAGOMTVWIYPLE-UHFFFAOYSA-N 0.000 description 1
- SVWWNEYBEFASMP-UHFFFAOYSA-N COC(c1cc(N)ncc1)=O Chemical compound COC(c1cc(N)ncc1)=O SVWWNEYBEFASMP-UHFFFAOYSA-N 0.000 description 1
- ORUMXWAUZBTDLW-UHFFFAOYSA-N COc(c(N)n1)cnc1Cl Chemical compound COc(c(N)n1)cnc1Cl ORUMXWAUZBTDLW-UHFFFAOYSA-N 0.000 description 1
- XIRAVAIKBDVKPX-UHFFFAOYSA-N COc1ncccc1-c1cc2ncc(-c3cccc(NC(NCC(F)(F)F)=O)c3)[n]2cc1 Chemical compound COc1ncccc1-c1cc2ncc(-c3cccc(NC(NCC(F)(F)F)=O)c3)[n]2cc1 XIRAVAIKBDVKPX-UHFFFAOYSA-N 0.000 description 1
- NSQGTWUODJNQQQ-UHFFFAOYSA-N Cc(cc[n]12)cc1ncc2[AlH2] Chemical compound Cc(cc[n]12)cc1ncc2[AlH2] NSQGTWUODJNQQQ-UHFFFAOYSA-N 0.000 description 1
- QDAHTDOYLDSDTB-UHFFFAOYSA-N Cc1c(-c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)nncc1 Chemical compound Cc1c(-c2cc3ncc(-c4cccc(NC(NCC(F)(F)F)=O)c4)[n]3cc2)nncc1 QDAHTDOYLDSDTB-UHFFFAOYSA-N 0.000 description 1
- QXPJYIKLTOCALW-UHFFFAOYSA-N Cc1nc(-c(cc[n]23)cc2ncc3I)nnc1C Chemical compound Cc1nc(-c(cc[n]23)cc2ncc3I)nnc1C QXPJYIKLTOCALW-UHFFFAOYSA-N 0.000 description 1
- RDQAHAZMXNMQOV-UHFFFAOYSA-N Cc1nc(-c2cc3ncc[n]3cc2)nnc1C Chemical compound Cc1nc(-c2cc3ncc[n]3cc2)nnc1C RDQAHAZMXNMQOV-UHFFFAOYSA-N 0.000 description 1
- BRQWTVSJEXYHIA-UHFFFAOYSA-N Cc1nnc(-c2cc3ncc(-c4cccc(NC(NC5CC5)=O)c4)[n]3cc2)[o]1 Chemical compound Cc1nnc(-c2cc3ncc(-c4cccc(NC(NC5CC5)=O)c4)[n]3cc2)[o]1 BRQWTVSJEXYHIA-UHFFFAOYSA-N 0.000 description 1
- DQOSMLNBDBVIIW-UHFFFAOYSA-N Fc(cc1)ccc1-c(cc[n]12)cc1ncc2I Chemical compound Fc(cc1)ccc1-c(cc[n]12)cc1ncc2I DQOSMLNBDBVIIW-UHFFFAOYSA-N 0.000 description 1
- YUCQBFNKZSOPNH-UHFFFAOYSA-N Fc(cc1)ccc1-c1cc2ncc[n]2cc1 Chemical compound Fc(cc1)ccc1-c1cc2ncc[n]2cc1 YUCQBFNKZSOPNH-UHFFFAOYSA-N 0.000 description 1
- ZQLZNGUJOGWVCB-UHFFFAOYSA-N NC(c1cc2ncc[n]2cc1)=O Chemical compound NC(c1cc2ncc[n]2cc1)=O ZQLZNGUJOGWVCB-UHFFFAOYSA-N 0.000 description 1
- ZRJJXXDQIQFZBW-UHFFFAOYSA-N Nc1nccc(CO)c1 Chemical compound Nc1nccc(CO)c1 ZRJJXXDQIQFZBW-UHFFFAOYSA-N 0.000 description 1
- RQMWVVBHJMUJNZ-UHFFFAOYSA-N Nc1nccc(Cl)c1 Chemical compound Nc1nccc(Cl)c1 RQMWVVBHJMUJNZ-UHFFFAOYSA-N 0.000 description 1
- OPDRNIZRTJOIEJ-UHFFFAOYSA-N Nc1nnc(C2OCCC2)[s]1 Chemical compound Nc1nnc(C2OCCC2)[s]1 OPDRNIZRTJOIEJ-UHFFFAOYSA-N 0.000 description 1
- LDAQJIOPNUEWIZ-UHFFFAOYSA-N O=C(NCC(F)(F)F)Nc1cc(-c2cnc3[n]2ccc(-c2ccc(N4CCCCC4)nn2)c3)ccc1 Chemical compound O=C(NCC(F)(F)F)Nc1cc(-c2cnc3[n]2ccc(-c2ccc(N4CCCCC4)nn2)c3)ccc1 LDAQJIOPNUEWIZ-UHFFFAOYSA-N 0.000 description 1
- JYVLKIIQYXAJSZ-UHFFFAOYSA-N OCc1cc2ncc[n]2cc1 Chemical compound OCc1cc2ncc[n]2cc1 JYVLKIIQYXAJSZ-UHFFFAOYSA-N 0.000 description 1
- XMXXTOPHCHQSIJ-UHFFFAOYSA-N [AlH2]c1cnc2[n]1ccc(Cl)c2 Chemical compound [AlH2]c1cnc2[n]1ccc(Cl)c2 XMXXTOPHCHQSIJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
-
- 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
- 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
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US6118408P | 2008-06-13 | 2008-06-13 | |
| US61/061,184 | 2008-06-13 | ||
| GB0810902.7 | 2008-06-13 | ||
| GBGB0810902.7A GB0810902D0 (en) | 2008-06-13 | 2008-06-13 | New compounds |
| PCT/EP2009/057318 WO2009150240A1 (en) | 2008-06-13 | 2009-06-12 | Imidazopyridine derivatives as inhibitors of receptor tyrosine kinases |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011522866A JP2011522866A (ja) | 2011-08-04 |
| JP2011522866A5 JP2011522866A5 (OSRAM) | 2012-05-17 |
| JP5596023B2 true JP5596023B2 (ja) | 2014-09-24 |
Family
ID=39672279
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011512999A Expired - Fee Related JP5596023B2 (ja) | 2008-06-13 | 2009-06-12 | レセプターチロシンキナーゼのインヒビターとしてのイミダゾピリジン誘導体 |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US8796244B2 (OSRAM) |
| EP (1) | EP2300465B1 (OSRAM) |
| JP (1) | JP5596023B2 (OSRAM) |
| KR (1) | KR101745730B1 (OSRAM) |
| CN (1) | CN102137859B (OSRAM) |
| AU (1) | AU2009256584B2 (OSRAM) |
| BR (1) | BRPI0915084B8 (OSRAM) |
| CA (1) | CA2727062A1 (OSRAM) |
| DK (1) | DK2300465T3 (OSRAM) |
| ES (1) | ES2735979T3 (OSRAM) |
| GB (1) | GB0810902D0 (OSRAM) |
| HR (1) | HRP20191027T1 (OSRAM) |
| HU (1) | HUE045300T2 (OSRAM) |
| IL (1) | IL209864A (OSRAM) |
| LT (1) | LT2300465T (OSRAM) |
| MX (1) | MX2010013743A (OSRAM) |
| NZ (1) | NZ589781A (OSRAM) |
| RU (1) | RU2518089C2 (OSRAM) |
| SI (1) | SI2300465T1 (OSRAM) |
| WO (1) | WO2009150240A1 (OSRAM) |
| ZA (1) | ZA201008961B (OSRAM) |
Families Citing this family (68)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101679409B (zh) | 2006-12-22 | 2014-11-26 | Astex治疗学有限公司 | 双环杂环衍生化合物、其医药组合物和其用途 |
| AU2007337886C1 (en) | 2006-12-22 | 2014-10-16 | Astex Therapeutics Limited | Bicyclic heterocyclic compounds as FGFR inhibitors |
| GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
| GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
| GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
| US8729074B2 (en) | 2009-03-20 | 2014-05-20 | Amgen Inc. | Inhibitors of PI3 kinase |
| GB0906472D0 (en) | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| GB0906470D0 (en) * | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| WO2011104731A1 (en) * | 2010-02-26 | 2011-09-01 | Decode Genetics Ehf | Genetic variants as markers for use in urinary bladder cancer risk assessment, diagnosis, prognosis and treatment |
| WO2012088266A2 (en) | 2010-12-22 | 2012-06-28 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of fgfr3 |
| EP2727920B1 (en) | 2011-07-29 | 2016-11-02 | FUJIFILM Corporation | 1,5-naphthyridine derivative or salt thereof |
| UA111382C2 (uk) | 2011-10-10 | 2016-04-25 | Оріон Корпорейшн | Інгібітори протеїнкінази |
| CN103214481B (zh) * | 2012-01-21 | 2016-08-03 | 中国科学院上海药物研究所 | 新型咪唑并[1,2-a]吡啶类化合物、其制备方法、包含此类化合物的药物组合物及其用途 |
| SI2861595T1 (sl) | 2012-06-13 | 2017-04-26 | Incyte Holdings Corporation | Substituirane triciklične spojine kot inhibitorji fgfr |
| CN102786543B (zh) * | 2012-07-24 | 2016-04-27 | 上海瑞博化学有限公司 | 咪唑并[1,2-a]吡啶-6-硼酸频哪醇酯及其衍生物的制备方法 |
| US9388185B2 (en) | 2012-08-10 | 2016-07-12 | Incyte Holdings Corporation | Substituted pyrrolo[2,3-b]pyrazines as FGFR inhibitors |
| US8729263B2 (en) | 2012-08-13 | 2014-05-20 | Novartis Ag | 1,4-disubstituted pyridazine analogs there of and methods for treating SMN-deficiency-related conditions |
| CA2886187C (en) * | 2012-09-28 | 2020-04-14 | Vanderbilt University | Fused heterocyclic compounds as selective bmp inhibitors |
| US9266892B2 (en) | 2012-12-19 | 2016-02-23 | Incyte Holdings Corporation | Fused pyrazoles as FGFR inhibitors |
| US9676754B2 (en) | 2012-12-20 | 2017-06-13 | Inception 2, Inc. | Triazolone compounds and uses thereof |
| CN103923078A (zh) * | 2013-01-15 | 2014-07-16 | 华东理工大学 | 3,4-二取代(1H-吡唑[3,4-b]吡啶)类化合物及其用途 |
| AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
| WO2014140073A1 (en) * | 2013-03-13 | 2014-09-18 | F. Hoffmann-La Roche Ag | Process for making benzoxazepin compounds |
| LT2986610T (lt) | 2013-04-19 | 2018-04-10 | Incyte Holdings Corporation | Bicikliniai heterociklai, kaip fgfr inhibitoriai |
| MX383686B (es) | 2013-07-31 | 2025-03-14 | Novartis Ag | Derivados de piridazina 1,4-disustituida, y su uso para el tratamiento de afecciones relacionadas con la deficiencia de smn. |
| BR112016014412A2 (pt) | 2013-12-20 | 2017-08-08 | Signal Pharm Llc | Compostos de diaminopirimidil substituído, composições do mesmo, e métodos de tratamento com o mesmo |
| ES2883289T3 (es) * | 2013-12-20 | 2021-12-07 | Astex Therapeutics Ltd | Compuestos heterocíclicos bicíclicos y sus usos en terapia |
| MX369646B (es) | 2014-08-18 | 2019-11-15 | Eisai R&D Man Co Ltd | Sal de derivado de piridina monociclico y su cristal. |
| US10851105B2 (en) | 2014-10-22 | 2020-12-01 | Incyte Corporation | Bicyclic heterocycles as FGFR4 inhibitors |
| MA41551A (fr) | 2015-02-20 | 2017-12-26 | Incyte Corp | Hétérocycles bicycliques utilisés en tant qu'inhibiteurs de fgfr4 |
| WO2016134294A1 (en) | 2015-02-20 | 2016-08-25 | Incyte Corporation | Bicyclic heterocycles as fgfr4 inhibitors |
| SG10201913036RA (en) | 2015-02-20 | 2020-02-27 | Incyte Corp | Bicyclic heterocycles as fgfr inhibitors |
| WO2016152996A1 (ja) * | 2015-03-24 | 2016-09-29 | 株式会社ダイセル | 超臨界流体クロマトグラフィー用の固定相 |
| WO2016152907A1 (ja) | 2015-03-25 | 2016-09-29 | 国立研究開発法人国立がん研究センター | 胆管癌治療剤 |
| US10077289B2 (en) | 2015-03-31 | 2018-09-18 | Allergan, Inc. | Cyclosporins modified on the MeBmt sidechain by heterocyclic rings |
| US11773106B2 (en) | 2015-10-16 | 2023-10-03 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US12365689B2 (en) | 2015-10-16 | 2025-07-22 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-n-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| US11365198B2 (en) | 2015-10-16 | 2022-06-21 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-a]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| RU2018117889A (ru) | 2015-10-16 | 2019-11-20 | Эббви Инк. | СПОСОБЫ ПОЛУЧЕНИЯ (3S,4R)-3-ЭТИЛ-4-(3H-ИМИДАЗО[1,2-a]ПИРРОЛО[2,3-e]-ПИРАЗИН-8-ИЛ)-N-(2,2,2-ТРИФТОРЭТИЛ)ПИРРОЛИДИН-1-КАРБОКСАМИДА И ЕГО ТВЕРДОФАЗНЫХ ФОРМ |
| US10550126B2 (en) | 2015-10-16 | 2020-02-04 | Abbvie Inc. | Processes for the preparation of (3S,4R)-3-ethyl-4-(3H-imidazo[1,2-A]pyrrolo[2,3-e]-pyrazin-8-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide and solid state forms thereof |
| CN108367000A (zh) | 2015-12-17 | 2018-08-03 | 卫材R&D管理有限公司 | 用于乳腺癌的治疗剂 |
| CN109952293A (zh) * | 2016-09-14 | 2019-06-28 | 范德比尔特大学 | Bmp信号转导的抑制、化合物、组合物及其用途 |
| AR111960A1 (es) | 2017-05-26 | 2019-09-04 | Incyte Corp | Formas cristalinas de un inhibidor de fgfr y procesos para su preparación |
| CN109776401A (zh) * | 2017-11-14 | 2019-05-21 | 成都博腾药业有限公司 | 一种制备6-氯-5-三氟甲基-2-氨基吡啶的方法 |
| ES2908283T3 (es) | 2017-12-02 | 2022-04-28 | Galapagos Nv | Nuevos compuestos y composiciones farmacéuticas de los mismos para el tratamiento de enfermedades |
| US10745400B2 (en) | 2018-03-14 | 2020-08-18 | Vanderbuilt University | Inhibition of BMP signaling, compounds, compositions and uses thereof |
| WO2019189241A1 (ja) | 2018-03-28 | 2019-10-03 | エーザイ・アール・アンド・ディー・マネジメント株式会社 | 肝細胞癌治療剤 |
| PL3788047T3 (pl) | 2018-05-04 | 2025-04-14 | Incyte Corporation | Stałe postacie inhibitora fgfr i sposoby ich otrzymywania |
| KR20210018264A (ko) | 2018-05-04 | 2021-02-17 | 인사이트 코포레이션 | Fgfr 억제제의 염 |
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| ES2735979T3 (es) | 2019-12-23 |
| SI2300465T1 (sl) | 2019-08-30 |
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| GB0810902D0 (en) | 2008-07-23 |
| CN102137859A (zh) | 2011-07-27 |
| CN102137859B (zh) | 2015-07-01 |
| BRPI0915084A2 (pt) | 2015-10-27 |
| RU2518089C2 (ru) | 2014-06-10 |
| BRPI0915084B1 (pt) | 2020-02-11 |
| LT2300465T (lt) | 2019-06-25 |
| WO2009150240A1 (en) | 2009-12-17 |
| EP2300465A1 (en) | 2011-03-30 |
| KR20110017000A (ko) | 2011-02-18 |
| US8796244B2 (en) | 2014-08-05 |
| US20120208791A1 (en) | 2012-08-16 |
| JP2011522866A (ja) | 2011-08-04 |
| IL209864A0 (en) | 2011-02-28 |
| BRPI0915084B8 (pt) | 2021-05-25 |
| RU2011100786A (ru) | 2012-07-20 |
| HRP20191027T1 (hr) | 2019-11-29 |
| AU2009256584B2 (en) | 2014-06-12 |
| KR101745730B1 (ko) | 2017-06-12 |
| DK2300465T3 (da) | 2019-06-24 |
| HUE045300T2 (hu) | 2019-12-30 |
| AU2009256584A1 (en) | 2009-12-17 |
| IL209864A (en) | 2015-10-29 |
| CA2727062A1 (en) | 2009-12-17 |
| ZA201008961B (en) | 2015-05-27 |
| EP2300465B1 (en) | 2019-04-17 |
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