PE20250776A1 - Sales y formas solidas de un inhibidor de fgfr y procesos para su preparacion - Google Patents
Sales y formas solidas de un inhibidor de fgfr y procesos para su preparacionInfo
- Publication number
- PE20250776A1 PE20250776A1 PE2024001456A PE2024001456A PE20250776A1 PE 20250776 A1 PE20250776 A1 PE 20250776A1 PE 2024001456 A PE2024001456 A PE 2024001456A PE 2024001456 A PE2024001456 A PE 2024001456A PE 20250776 A1 PE20250776 A1 PE 20250776A1
- Authority
- PE
- Peru
- Prior art keywords
- salts
- preparation
- solid forms
- processes
- fgfr inhibitor
- Prior art date
Links
- 239000007787 solid Substances 0.000 title abstract 5
- 229940125829 fibroblast growth factor receptor inhibitor Drugs 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- 150000003839 salts Chemical group 0.000 abstract 2
- ZBHJWDKPRTVNKG-VQTJNVASSA-N CC1=C(C=CC=C1C)C1=C(C=C2C(=N1)C(=NN2)C=1C=CC(=NC=1)N1C[C@H]2N(CC1)C[C@@H](C2)O)OC Chemical compound CC1=C(C=CC=C1C)C1=C(C=C2C(=N1)C(=NN2)C=1C=CC(=NC=1)N1C[C@H]2N(CC1)C[C@@H](C2)O)OC ZBHJWDKPRTVNKG-VQTJNVASSA-N 0.000 abstract 1
- 108091008794 FGF receptors Proteins 0.000 abstract 1
- 206010028980 Neoplasm Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 229940125904 compound 1 Drugs 0.000 abstract 1
- 150000001875 compounds Chemical group 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 102000052178 fibroblast growth factor receptor activity proteins Human genes 0.000 abstract 1
- 230000001404 mediated effect Effects 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- 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
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
La presente invencion se refiere a sales y formas solidas del inhibidor de FGFR (7R,8aS)-2-(5-(5-(2,3-dimetilfenil)-6-metoxi-1H-pirazolo[4,3-b]piridin-3-il)piridin-2-il)octahidropirrolo[1,2-a]pirazin-7-ol, e incluye metodos para su preparacion, en donde los compuestos, las sales y las formas solidas son utiles en el tratamiento de enfermedades mediadas por FGFR, tales como el cancer. En particular, hace referencia a una forma solida del Compuesto 1 con la formula (I) en donde la forma solida es cristalina.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202163292628P | 2021-12-22 | 2021-12-22 | |
PCT/US2022/053582 WO2023122134A1 (en) | 2021-12-22 | 2022-12-21 | Salts and solid forms of an fgfr inhibitor and processes of preparing thereof |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20250776A1 true PE20250776A1 (es) | 2025-03-14 |
Family
ID=85172903
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2024001456A PE20250776A1 (es) | 2021-12-22 | 2022-12-21 | Sales y formas solidas de un inhibidor de fgfr y procesos para su preparacion |
Country Status (15)
Country | Link |
---|---|
US (1) | US20230192722A1 (es) |
EP (1) | EP4452982A1 (es) |
JP (1) | JP2025500466A (es) |
KR (1) | KR20240136984A (es) |
CN (1) | CN118660889A (es) |
AR (1) | AR128043A1 (es) |
AU (1) | AU2022418585A1 (es) |
CL (1) | CL2024001873A1 (es) |
CO (1) | CO2024009568A2 (es) |
CR (1) | CR20240297A (es) |
IL (1) | IL313735A (es) |
MX (1) | MX2024007951A (es) |
PE (1) | PE20250776A1 (es) |
TW (1) | TW202340215A (es) |
WO (1) | WO2023122134A1 (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2021067374A1 (en) | 2019-10-01 | 2021-04-08 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
CR20230467A (es) | 2021-03-10 | 2024-02-20 | Jnana Therapeutics Inc | Inhibidores de molécula pequeña de la función de slc6a19 de mamífero |
Family Cites Families (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5521184A (en) | 1992-04-03 | 1996-05-28 | Ciba-Geigy Corporation | Pyrimidine derivatives and processes for the preparation thereof |
AU5620299A (en) | 1998-08-11 | 2000-03-06 | Novartis Ag | Isoquinoline derivatives with angiogenesis inhibiting activity |
US6133031A (en) | 1999-08-19 | 2000-10-17 | Isis Pharmaceuticals Inc. | Antisense inhibition of focal adhesion kinase expression |
GB9905075D0 (en) | 1999-03-06 | 1999-04-28 | Zeneca Ltd | Chemical compounds |
GB0004890D0 (en) | 2000-03-01 | 2000-04-19 | Astrazeneca Uk Ltd | Chemical compounds |
ES2225624T3 (es) | 2000-06-28 | 2005-03-16 | Smithkline Beecham Plc | Procedimiento de molienda por via humeda. |
WO2003024967A2 (en) | 2001-09-19 | 2003-03-27 | Aventis Pharma S.A. | Indolizines as kinase protein inhibitors |
CA2462657C (en) | 2001-10-30 | 2011-04-26 | Novartis Ag | Staurosporine derivatives as inhibitors of flt3 receptor tyrosine kinase activity |
CA2466279A1 (en) | 2001-11-13 | 2003-05-22 | Dana-Farber Cancer Institute, Inc. | Agents that modulate immune cell activation and methods of use thereof |
WO2003062236A1 (en) | 2002-01-22 | 2003-07-31 | Warner-Lambert Company Llc | 2-(PYRIDIN-2-YLAMINO)-PYRIDO[2,3d]PYRIMIDIN-7-ONES |
TW200406374A (en) | 2002-05-29 | 2004-05-01 | Novartis Ag | Diaryl urea derivatives useful for the treatment of protein kinase dependent diseases |
GB0215676D0 (en) | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
AR042052A1 (es) | 2002-11-15 | 2005-06-08 | Vertex Pharma | Diaminotriazoles utiles como inhibidores de proteinquinasas |
UA80767C2 (en) | 2002-12-20 | 2007-10-25 | Pfizer Prod Inc | Pyrimidine derivatives for the treatment of abnormal cell growth |
CA2508660C (en) | 2002-12-23 | 2013-08-20 | Wyeth | Antibodies against pd-1 and uses therefor |
GB0305929D0 (en) | 2003-03-14 | 2003-04-23 | Novartis Ag | Organic compounds |
AR045944A1 (es) | 2003-09-24 | 2005-11-16 | Novartis Ag | Derivados de isoquinolina 1.4-disustituidas |
CN101106983A (zh) | 2004-11-24 | 2008-01-16 | 诺瓦提斯公司 | JAK抑制剂与至少一种Bcr-Abl、Flt-3、FAK或RAF激酶抑制剂的组合 |
DK2439273T3 (da) | 2005-05-09 | 2019-06-03 | Ono Pharmaceutical Co | Humane monoklonale antistoffer til programmeret død-1(pd-1) og fremgangsmåder til behandling af cancer ved anvendelse af anti-pd-1- antistoffer alene eller i kombination med andre immunterapeutika |
CN104356236B (zh) | 2005-07-01 | 2020-07-03 | E.R.施贵宝&圣斯有限责任公司 | 抗程序性死亡配体1(pd-l1)的人单克隆抗体 |
BR122017025062B8 (pt) | 2007-06-18 | 2021-07-27 | Merck Sharp & Dohme | anticorpo monoclonal ou fragmento de anticorpo para o receptor de morte programada humano pd-1, polinucleotídeo e composição compreendendo o referido anticorpo ou fragmento |
CA2709202C (en) | 2007-12-19 | 2013-04-23 | Amgen Inc. | Fused pyridine, pyrimidine and triazine compounds as cell cycle inhibitors |
US8168757B2 (en) | 2008-03-12 | 2012-05-01 | Merck Sharp & Dohme Corp. | PD-1 binding proteins |
EP3530672B1 (en) | 2008-09-26 | 2024-05-01 | Dana-Farber Cancer Institute, Inc. | Human anti-pd-1, pd-l1, and pd-l2 antibodies and uses thereof |
RU2017132160A (ru) | 2008-12-09 | 2019-02-08 | Дженентек, Инк. | Антитела к pd-l1 и их применение для усиления функции t-клеток |
JO2885B1 (en) | 2008-12-22 | 2015-03-15 | ايلي ليلي اند كومباني | Protein kinase inhibitors |
EP2393835B1 (en) | 2009-02-09 | 2017-04-05 | Université d'Aix-Marseille | Pd-1 antibodies and pd-l1 antibodies and uses thereof |
EP2504028A4 (en) | 2009-11-24 | 2014-04-09 | Amplimmune Inc | SIMULTANEOUS INHIBITION OF PD-L1 / PD-L2 |
WO2011082400A2 (en) | 2010-01-04 | 2011-07-07 | President And Fellows Of Harvard College | Modulators of immunoinhibitory receptor pd-1, and methods of use thereof |
UY33227A (es) | 2010-02-19 | 2011-09-30 | Novartis Ag | Compuestos de pirrolopirimidina como inhibidores de la cdk4/6 |
WO2011159877A2 (en) | 2010-06-18 | 2011-12-22 | The Brigham And Women's Hospital, Inc. | Bi-specific antibodies against tim-3 and pd-1 for immunotherapy in chronic immune conditions |
US8907053B2 (en) | 2010-06-25 | 2014-12-09 | Aurigene Discovery Technologies Limited | Immunosuppression modulating compounds |
HRP20161092T1 (hr) | 2010-10-25 | 2016-10-21 | G1 Therapeutics, Inc. | Cdk inhibitori |
MY161199A (en) | 2011-03-23 | 2017-04-14 | Amgen Inc | Fused tricyclic dual inhibitors of cdk 4/6 and flt3 |
HUE056201T2 (hu) | 2015-07-30 | 2022-02-28 | Macrogenics Inc | PD-1-hez kötõdõ molekulák és alkalmazásukra szolgáló eljárások |
WO2017070089A1 (en) | 2015-10-19 | 2017-04-27 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
DK3377488T3 (da) | 2015-11-19 | 2022-10-03 | Incyte Corp | Heterocykliske forbindelser som immunomodulatorer |
WO2017106634A1 (en) | 2015-12-17 | 2017-06-22 | Incyte Corporation | N-phenyl-pyridine-2-carboxamide derivatives and their use as pd-1/pd-l1 protein/protein interaction modulators |
HUE052722T2 (hu) | 2015-12-22 | 2021-05-28 | Incyte Corp | Heterociklusos vegyületek mint immunomodulátorok |
ES2906460T3 (es) | 2016-05-06 | 2022-04-18 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
TW201808902A (zh) | 2016-05-26 | 2018-03-16 | 美商英塞特公司 | 作為免疫調節劑之雜環化合物 |
EP3472167B1 (en) | 2016-06-20 | 2022-08-03 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
MA45669A (fr) | 2016-07-14 | 2019-05-22 | Incyte Corp | Composés hétérocycliques utilisés comme immunomodulateurs |
ES2941716T3 (es) | 2016-08-29 | 2023-05-25 | Incyte Corp | Compuestos heterocíclicos como inmunomoduladores |
EP3558989B1 (en) | 2016-12-22 | 2021-04-14 | Incyte Corporation | Triazolo[1,5-a]pyridine derivatives as immunomodulators |
MX391980B (es) | 2016-12-22 | 2025-03-21 | Incyte Corp | Derivados de tetrahidro imidazo [4,5-c] piridina como inductores de internalización de ligando 1 de muerte programada (pd-l1). |
WO2018119263A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Heterocyclic compounds derivatives as pd-l1 internalization inducers |
MX391981B (es) | 2016-12-22 | 2025-03-21 | Incyte Corp | Derivados de benzooxazol como inmunomoduladores. |
US20180179202A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Heterocyclic compounds as immunomodulators |
WO2018119221A1 (en) | 2016-12-22 | 2018-06-28 | Incyte Corporation | Pyridine derivatives as immunomodulators |
UA128453C2 (uk) | 2018-03-30 | 2024-07-17 | Інсайт Корпорейшн | Гетероциклічні сполуки як імуномодулятори |
HRP20230306T1 (hr) | 2018-05-11 | 2023-05-12 | Incyte Corporation | Derivati tetrahidro-imidazo[4,5-c]piridina kao pd-l1 imunomodulatori |
CA3157361A1 (en) | 2019-10-14 | 2021-04-22 | Incyte Corporation | Bicyclic heterocycles as fgfr inhibitors |
-
2022
- 2022-12-21 CN CN202280091209.6A patent/CN118660889A/zh active Pending
- 2022-12-21 KR KR1020247024528A patent/KR20240136984A/ko active Pending
- 2022-12-21 AR ARP220103523A patent/AR128043A1/es unknown
- 2022-12-21 MX MX2024007951A patent/MX2024007951A/es unknown
- 2022-12-21 WO PCT/US2022/053582 patent/WO2023122134A1/en active Application Filing
- 2022-12-21 EP EP22854263.5A patent/EP4452982A1/en active Pending
- 2022-12-21 AU AU2022418585A patent/AU2022418585A1/en active Pending
- 2022-12-21 PE PE2024001456A patent/PE20250776A1/es unknown
- 2022-12-21 CR CR20240297A patent/CR20240297A/es unknown
- 2022-12-21 JP JP2024538174A patent/JP2025500466A/ja active Pending
- 2022-12-21 IL IL313735A patent/IL313735A/en unknown
- 2022-12-21 US US18/085,814 patent/US20230192722A1/en active Pending
- 2022-12-21 TW TW111149106A patent/TW202340215A/zh unknown
-
2024
- 2024-06-19 CL CL2024001873A patent/CL2024001873A1/es unknown
- 2024-07-19 CO CONC2024/0009568A patent/CO2024009568A2/es unknown
Also Published As
Publication number | Publication date |
---|---|
TW202340215A (zh) | 2023-10-16 |
AU2022418585A1 (en) | 2024-07-11 |
MX2024007951A (es) | 2024-07-10 |
EP4452982A1 (en) | 2024-10-30 |
AR128043A1 (es) | 2024-03-20 |
CN118660889A (zh) | 2024-09-17 |
US20230192722A1 (en) | 2023-06-22 |
WO2023122134A1 (en) | 2023-06-29 |
CO2024009568A2 (es) | 2024-07-29 |
JP2025500466A (ja) | 2025-01-09 |
CR20240297A (es) | 2024-09-18 |
KR20240136984A (ko) | 2024-09-19 |
IL313735A (en) | 2024-08-01 |
CL2024001873A1 (es) | 2024-12-06 |
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