MX2020006293A - Derivados de 5-(2-2,5-difluorofenil)pirrolidin-1-il)-3-(1h-pirazol -1-il)pirazolo[1,5-a]pirimidina y compuestos relacionados como inhibidores de trk cinasa para el tratamiento de cancer. - Google Patents
Derivados de 5-(2-2,5-difluorofenil)pirrolidin-1-il)-3-(1h-pirazol -1-il)pirazolo[1,5-a]pirimidina y compuestos relacionados como inhibidores de trk cinasa para el tratamiento de cancer.Info
- Publication number
- MX2020006293A MX2020006293A MX2020006293A MX2020006293A MX2020006293A MX 2020006293 A MX2020006293 A MX 2020006293A MX 2020006293 A MX2020006293 A MX 2020006293A MX 2020006293 A MX2020006293 A MX 2020006293A MX 2020006293 A MX2020006293 A MX 2020006293A
- Authority
- MX
- Mexico
- Prior art keywords
- treating cancer
- kinase inhibitors
- difluorophenyl
- pyrazol
- pyrrolidin
- Prior art date
Links
- 206010028980 Neoplasm Diseases 0.000 title abstract 2
- 201000011510 cancer Diseases 0.000 title abstract 2
- 229940043355 kinase inhibitor Drugs 0.000 title abstract 2
- 239000003757 phosphotransferase inhibitor Substances 0.000 title abstract 2
- FWDOVLGKHCXRFF-UHFFFAOYSA-N FC1=C(C=C(C=C1)F)C1N(CCC1)C1=NC=2N(C=C1)N=CC=2N1N=CC=C1 Chemical class FC1=C(C=C(C=C1)F)C1N(CCC1)C1=NC=2N(C=C1)N=CC=2N1N=CC=C1 FWDOVLGKHCXRFF-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 208000027866 inflammatory disease Diseases 0.000 abstract 1
- LDIJKUBTLZTFRG-UHFFFAOYSA-N pyrazolo[1,5-a]pyrimidine Chemical class N1=CC=CN2N=CC=C21 LDIJKUBTLZTFRG-UHFFFAOYSA-N 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
La solicitud hace referencia a derivados de pirazolo[1,5-a]pirimid ina de la fórmula (IV) como inhibidores de Trk cinasa para el tratamiento de cáncer y enfermedades inflamatorias.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201762599490P | 2017-12-15 | 2017-12-15 | |
PCT/US2018/065187 WO2019118584A1 (en) | 2017-12-15 | 2018-12-12 | 5-(2-(2,5-difluorophenyl)pyrrolidin-1 -yl)-3-(1h-pyrazol-1-yl)pyrazolo[1,5-a]pyrimidine derivatives and related compounds as trk kinase inhibitors for treating cancer |
Publications (1)
Publication Number | Publication Date |
---|---|
MX2020006293A true MX2020006293A (es) | 2020-12-03 |
Family
ID=65139120
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2020006293A MX2020006293A (es) | 2017-12-15 | 2018-12-12 | Derivados de 5-(2-2,5-difluorofenil)pirrolidin-1-il)-3-(1h-pirazol -1-il)pirazolo[1,5-a]pirimidina y compuestos relacionados como inhibidores de trk cinasa para el tratamiento de cancer. |
Country Status (24)
Country | Link |
---|---|
US (3) | US11230546B2 (es) |
EP (2) | EP3724191B9 (es) |
JP (1) | JP7321183B2 (es) |
KR (1) | KR20200099557A (es) |
CN (1) | CN111819179B (es) |
AU (1) | AU2018383571B2 (es) |
BR (1) | BR112020011775A2 (es) |
CA (1) | CA3084814A1 (es) |
DK (1) | DK3724191T3 (es) |
EA (1) | EA202091475A1 (es) |
ES (1) | ES2908773T3 (es) |
HR (1) | HRP20220464T1 (es) |
HU (1) | HUE059313T2 (es) |
IL (1) | IL275059B2 (es) |
LT (1) | LT3724191T (es) |
MX (1) | MX2020006293A (es) |
PL (1) | PL3724191T3 (es) |
PT (1) | PT3724191T (es) |
SA (1) | SA520412192B1 (es) |
SG (1) | SG11202005237SA (es) |
SI (1) | SI3724191T1 (es) |
TW (1) | TW201936194A (es) |
WO (1) | WO2019118584A1 (es) |
ZA (2) | ZA202003483B (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW201936194A (zh) | 2017-12-15 | 2019-09-16 | 美商金字塔生技公司 | 肌旋蛋白激酶抑制劑 |
GB201813791D0 (en) * | 2018-08-23 | 2018-10-10 | Benevolental Bio Ltd | Organic compounds |
EP3932923B1 (en) * | 2019-03-19 | 2023-05-03 | Central China Normal University | Pyrazolopyrimidine compound, pharmaceutical composition, and application therefor |
CN111718350B (zh) * | 2019-03-19 | 2021-04-13 | 华中师范大学 | 吡唑取代的吡唑并嘧啶化合物和药物组合物及其应用 |
CN111848626B (zh) * | 2019-04-30 | 2021-11-30 | 江苏柯菲平医药股份有限公司 | Trk激酶抑制剂及其用途 |
CN112979654B (zh) * | 2019-12-16 | 2024-03-19 | 赛诺哈勃药业(成都)有限公司 | 杂芳基稠环化合物、其制备方法及应用 |
CA3172681A1 (en) * | 2020-04-15 | 2021-10-21 | Kollol Pal | Methods for preparing tyrosine receptor kinase inhibitors |
CN114437077B (zh) * | 2020-11-04 | 2024-01-30 | 浙江同源康医药股份有限公司 | 用作激酶抑制剂的化合物及其应用 |
CN114437075A (zh) * | 2020-11-03 | 2022-05-06 | 上海瑶琪生物科技有限公司 | 用作ntrk激酶抑制剂的化合物及其应用 |
KR102541026B1 (ko) * | 2020-11-11 | 2023-06-12 | 주식회사 한독 | Trk 억제제 화합물의 제조 방법 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8507488B2 (en) | 2008-05-13 | 2013-08-13 | Irm Llc | Fused nitrogen containing heterocycles and compositions thereof as kinase inhibitors |
DK3106463T6 (da) | 2008-10-22 | 2020-02-24 | Array Biopharma Inc | Pyrazolo[1,5-]pyrimidinforbindelse som trk-kinasehæmmer |
PE20131197A1 (es) | 2008-10-31 | 2013-11-06 | Genentech Inc | Compuestos de pirazolopirimidina como inhibidores de jak y composiciones farmaceuticas que los contienen |
EP2417138B1 (en) | 2009-04-09 | 2019-11-27 | Merck Sharp & Dohme Corp. | Pyrazolo[1, 5-a]pyrimidine derivatives as mtor inhibitors |
WO2012034095A1 (en) * | 2010-09-09 | 2012-03-15 | Irm Llc | Compounds and compositions as trk inhibitors |
WO2012125668A1 (en) * | 2011-03-17 | 2012-09-20 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
US20140288043A1 (en) | 2013-03-19 | 2014-09-25 | Genentech, Inc. | Pyrazolopyridine compounds |
WO2015143652A1 (en) | 2014-03-26 | 2015-10-01 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS,COMPOSITIONS AND METHODS THEREOF |
FR3029769A1 (fr) * | 2014-12-10 | 2016-06-17 | Tornier Sa | Kit pour une prothese d'epaule |
RU2708674C2 (ru) | 2014-12-15 | 2019-12-11 | СиЭмДжи ФАРМАСЬЮТИКАЛ КО., ЛТД. | Конденсированные кольцевые гетероарильные соединения и их применение в качестве ингибиторов trk |
TWI698436B (zh) | 2014-12-30 | 2020-07-11 | 美商佛瑪治療公司 | 作為泛素特異性蛋白酶7抑制劑之吡咯并及吡唑并嘧啶 |
JP6475084B2 (ja) | 2015-05-21 | 2019-02-27 | 臼井国際産業株式会社 | トルクセンサ用シャフトの製造設備およびその製造方法 |
TW201936194A (zh) | 2017-12-15 | 2019-09-16 | 美商金字塔生技公司 | 肌旋蛋白激酶抑制劑 |
CA3172681A1 (en) | 2020-04-15 | 2021-10-21 | Kollol Pal | Methods for preparing tyrosine receptor kinase inhibitors |
-
2018
- 2018-12-12 TW TW107144769A patent/TW201936194A/zh unknown
- 2018-12-12 US US16/772,253 patent/US11230546B2/en active Active
- 2018-12-12 HR HRP20220464TT patent/HRP20220464T1/hr unknown
- 2018-12-12 PT PT188369771T patent/PT3724191T/pt unknown
- 2018-12-12 EP EP18836977.1A patent/EP3724191B9/en active Active
- 2018-12-12 AU AU2018383571A patent/AU2018383571B2/en active Active
- 2018-12-12 JP JP2020551775A patent/JP7321183B2/ja active Active
- 2018-12-12 MX MX2020006293A patent/MX2020006293A/es unknown
- 2018-12-12 BR BR112020011775-7A patent/BR112020011775A2/pt unknown
- 2018-12-12 SI SI201830632T patent/SI3724191T1/sl unknown
- 2018-12-12 LT LTEPPCT/US2018/065187T patent/LT3724191T/lt unknown
- 2018-12-12 DK DK18836977.1T patent/DK3724191T3/da active
- 2018-12-12 ES ES18836977T patent/ES2908773T3/es active Active
- 2018-12-12 IL IL275059A patent/IL275059B2/en unknown
- 2018-12-12 CA CA3084814A patent/CA3084814A1/en active Pending
- 2018-12-12 EP EP22152688.2A patent/EP4053128A1/en active Pending
- 2018-12-12 WO PCT/US2018/065187 patent/WO2019118584A1/en active Application Filing
- 2018-12-12 KR KR1020207020360A patent/KR20200099557A/ko not_active Application Discontinuation
- 2018-12-12 EA EA202091475A patent/EA202091475A1/ru unknown
- 2018-12-12 SG SG11202005237SA patent/SG11202005237SA/en unknown
- 2018-12-12 PL PL18836977T patent/PL3724191T3/pl unknown
- 2018-12-12 HU HUE18836977A patent/HUE059313T2/hu unknown
- 2018-12-12 CN CN201880080978.XA patent/CN111819179B/zh active Active
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2020
- 2020-06-10 ZA ZA2020/03483A patent/ZA202003483B/en unknown
- 2020-06-13 SA SA520412192A patent/SA520412192B1/ar unknown
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2021
- 2021-11-23 US US17/533,954 patent/US20220235055A1/en not_active Abandoned
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2022
- 2022-05-27 ZA ZA2022/05900A patent/ZA202205900B/en unknown
- 2022-12-08 US US18/078,087 patent/US11739096B2/en active Active
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