JP7767301B2 - チロシン受容体キナーゼ阻害剤を調製する方法 - Google Patents

チロシン受容体キナーゼ阻害剤を調製する方法

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JP7767301B2
JP7767301B2 JP2022559980A JP2022559980A JP7767301B2 JP 7767301 B2 JP7767301 B2 JP 7767301B2 JP 2022559980 A JP2022559980 A JP 2022559980A JP 2022559980 A JP2022559980 A JP 2022559980A JP 7767301 B2 JP7767301 B2 JP 7767301B2
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alkyl
formula
hydrogen
haloalkyl
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JP2023522841A (ja
JP2023522841A5 (https=
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コロル パル
プラサント デブ
ハリ プラカシュ
アヴィナシュ ボルデ
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ピラミッド バイオサイエンシズ インコーポレイテッド
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole 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
    • C07D231/38Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic 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
    • C07D403/04Heterocyclic 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Medicines Containing Material From Animals Or Micro-Organisms (AREA)
JP2022559980A 2020-04-15 2021-04-15 チロシン受容体キナーゼ阻害剤を調製する方法 Active JP7767301B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202063010108P 2020-04-15 2020-04-15
US63/010,108 2020-04-15
PCT/US2021/027538 WO2021211882A1 (en) 2020-04-15 2021-04-15 Methods for preparing tyrosine receptor kinase inhibitors

Publications (3)

Publication Number Publication Date
JP2023522841A JP2023522841A (ja) 2023-06-01
JP2023522841A5 JP2023522841A5 (https=) 2024-04-26
JP7767301B2 true JP7767301B2 (ja) 2025-11-11

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JP2022559980A Active JP7767301B2 (ja) 2020-04-15 2021-04-15 チロシン受容体キナーゼ阻害剤を調製する方法

Country Status (12)

Country Link
US (1) US12606565B2 (https=)
EP (1) EP4135700A4 (https=)
JP (1) JP7767301B2 (https=)
KR (1) KR20230011912A (https=)
CN (1) CN115515591B (https=)
AU (1) AU2021255613A1 (https=)
BR (1) BR112022020114A2 (https=)
CA (1) CA3172681A1 (https=)
IL (1) IL296921A (https=)
MX (1) MX2022012437A (https=)
WO (1) WO2021211882A1 (https=)
ZA (1) ZA202209792B (https=)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SG11202005237SA (en) 2017-12-15 2020-07-29 Pyramid Biosciences Inc 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
IL296921A (en) 2020-04-15 2022-12-01 Pyramid Biosciences Inc Methods for making receptor tyrosine kinase inhibitors

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010504933A (ja) 2006-09-29 2010-02-18 ノバルティス アーゲー Pi3k脂質キナーゼ阻害剤としてのピラゾロピリミジン
JP2014520898A (ja) 2011-07-21 2014-08-25 トレロ ファーマシューティカルズ, インコーポレイテッド 複素環式プロテインキナーゼ阻害剤
JP2017538766A (ja) 2014-12-15 2017-12-28 シーエムジー ファーマシューティカル カンパニー,リミテッド 縮合環ヘテロアリール化合物及びtrk抑制剤としての用途
JP2018500376A (ja) 2014-12-30 2018-01-11 フォーマ セラピューティクス,インコーポレイテッド ユビキチン特異的プロテアーゼ7阻害薬としてのピロロ及びピラゾロピリミジン
WO2019118584A1 (en) 2017-12-15 2019-06-20 Pyramid Biosciences, Inc. 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

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US4911920A (en) 1986-07-30 1990-03-27 Alcon Laboratories, Inc. Sustained release, comfort formulation for glaucoma therapy
FR2588189B1 (fr) 1985-10-03 1988-12-02 Merck Sharp & Dohme Composition pharmaceutique de type a transition de phase liquide-gel
JP2594486B2 (ja) 1991-01-15 1997-03-26 アルコン ラボラトリーズ インコーポレイテッド 局所的眼薬組成物
US5212162A (en) 1991-03-27 1993-05-18 Alcon Laboratories, Inc. Use of combinations gelling polysaccharides and finely divided drug carrier substrates in topical ophthalmic compositions
CN101242844A (zh) * 2005-06-10 2008-08-13 詹森药业有限公司 作为激酶调节剂的氨基嘧啶类化合物
UA95244C2 (ru) * 2005-06-22 2011-07-25 Плексикон, Инк. Соединения и способ модулирования активности киназ, и показания для их применения
KR101324804B1 (ko) 2008-05-13 2013-11-01 아이알엠 엘엘씨 키나제 억제제로서의 질소 함유 융합 헤테로사이클 및 그의 조성물
MY169791A (en) 2008-10-22 2019-05-15 Array Biopharma Inc Substituted pyrazolo [1,5-a] pyrimidine compounds as trk kinase inhibitors
EP2348860B1 (en) 2008-10-31 2015-05-27 Genentech, Inc. Pyrazolopyrimidine jak inhibitor compounds and methods
WO2012022045A1 (en) * 2010-08-20 2012-02-23 Hutchison Medipharma Limited Pyrrolopyrimidine compounds and uses thereof
WO2014055928A2 (en) * 2012-10-04 2014-04-10 University Of Utah Research Foundation Substituted n-(3-(pyrimidin-4-yl)phenyl)acrylamide analogs as tyrosine receptor kinase btk inhibitors
FR3029769A1 (fr) 2014-12-10 2016-06-17 Tornier Sa Kit pour une prothese d'epaule
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
WO2018005533A1 (en) * 2016-07-01 2018-01-04 G1 Therapeutics, Inc. Antiproliferative pyrimidine-based compounds
IL296921A (en) 2020-04-15 2022-12-01 Pyramid Biosciences Inc Methods for making receptor tyrosine kinase inhibitors

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Publication number Priority date Publication date Assignee Title
JP2010504933A (ja) 2006-09-29 2010-02-18 ノバルティス アーゲー Pi3k脂質キナーゼ阻害剤としてのピラゾロピリミジン
JP2014520898A (ja) 2011-07-21 2014-08-25 トレロ ファーマシューティカルズ, インコーポレイテッド 複素環式プロテインキナーゼ阻害剤
JP2017538766A (ja) 2014-12-15 2017-12-28 シーエムジー ファーマシューティカル カンパニー,リミテッド 縮合環ヘテロアリール化合物及びtrk抑制剤としての用途
JP2018500376A (ja) 2014-12-30 2018-01-11 フォーマ セラピューティクス,インコーポレイテッド ユビキチン特異的プロテアーゼ7阻害薬としてのピロロ及びピラゾロピリミジン
WO2019118584A1 (en) 2017-12-15 2019-06-20 Pyramid Biosciences, Inc. 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

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
PubChem CID 64179089,2012年10月23日
Tetrahedron,2007年,63(3),p.748-753

Also Published As

Publication number Publication date
CA3172681A1 (en) 2021-10-21
WO2021211882A1 (en) 2021-10-21
EP4135700A4 (en) 2024-04-17
KR20230011912A (ko) 2023-01-25
US12606565B2 (en) 2026-04-21
US20230242536A1 (en) 2023-08-03
JP2023522841A (ja) 2023-06-01
AU2021255613A1 (en) 2022-09-29
CN115515591A (zh) 2022-12-23
EP4135700A1 (en) 2023-02-22
IL296921A (en) 2022-12-01
MX2022012437A (es) 2022-10-27
CN115515591B (zh) 2024-09-27
BR112022020114A2 (pt) 2022-11-29
ZA202209792B (en) 2025-01-29

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