CN115515591B - 用于制备酪氨酸受体激酶抑制剂的方法 - Google Patents

用于制备酪氨酸受体激酶抑制剂的方法 Download PDF

Info

Publication number
CN115515591B
CN115515591B CN202180024618.XA CN202180024618A CN115515591B CN 115515591 B CN115515591 B CN 115515591B CN 202180024618 A CN202180024618 A CN 202180024618A CN 115515591 B CN115515591 B CN 115515591B
Authority
CN
China
Prior art keywords
alkyl
compound
formula
haloalkyl
hydrogen
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.)
Active
Application number
CN202180024618.XA
Other languages
English (en)
Chinese (zh)
Other versions
CN115515591A (zh
Inventor
K·帕尔
P·戴波
H·普拉卡什
A·博尔德
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Paramid Biosciences
Original Assignee
Paramid Biosciences
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Paramid Biosciences filed Critical Paramid Biosciences
Publication of CN115515591A publication Critical patent/CN115515591A/zh
Application granted granted Critical
Publication of CN115515591B publication Critical patent/CN115515591B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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

Landscapes

  • 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)
CN202180024618.XA 2020-04-15 2021-04-15 用于制备酪氨酸受体激酶抑制剂的方法 Active CN115515591B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US202063010108P 2020-04-15 2020-04-15
US63/010108 2020-04-15
PCT/US2021/027538 WO2021211882A1 (en) 2020-04-15 2021-04-15 Methods for preparing tyrosine receptor kinase inhibitors

Publications (2)

Publication Number Publication Date
CN115515591A CN115515591A (zh) 2022-12-23
CN115515591B true CN115515591B (zh) 2024-09-27

Family

ID=78083713

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202180024618.XA Active CN115515591B (zh) 2020-04-15 2021-04-15 用于制备酪氨酸受体激酶抑制剂的方法

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 (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
WO2008037477A1 (en) 2006-09-29 2008-04-03 Novartis Ag Pyrazolopyrimidines as p13k lipid kinase inhibitors
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
EP3812387A1 (en) 2011-07-21 2021-04-28 Sumitomo Dainippon Pharma Oncology, Inc. Heterocyclic protein kinase inhibitors
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
CA2971024C (en) 2014-12-15 2023-09-26 Handok Inc. Fused ring heteroaryl compounds and their use as trk inhibitors
AR103297A1 (es) 2014-12-30 2017-05-03 Forma Therapeutics Inc Pirrolo y pirazolopirimidinas como inhibidores de la proteasa 7 específica de ubiquitina
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

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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

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
JP7767301B2 (ja) 2025-11-11
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
BR112022020114A2 (pt) 2022-11-29
ZA202209792B (en) 2025-01-29

Similar Documents

Publication Publication Date Title
AU2022202494B2 (en) Amine-substituted heterocyclic compounds as ehmt2 inhibitors and methods of use thereof
CA2952692C (en) Substituted imidazo[1,2b]pyridazine compounds
US6933294B2 (en) Thiophene-based tricyclic compounds and pharmaceutical compositions comprising same
CA3013618C (en) Substituted pyrazolo[1,5-a]pyrimidine compounds as trk kinase inhibitors
CN105814055B (zh) 作为tnf活性调节剂的稠合咪唑和吡唑衍生物
DK2725028T3 (en) Substituted pyrazolo [1,5-a] pyrimidine compounds as intermediates in the synthesis of kinase inhibitors TRK
AU2019222026A1 (en) Pyrimidine-fused cyclic compound, preparation method therefor and application thereof
WO2021244659A1 (zh) 同位素取代的螺芳环化合物及其应用
CN109195968B (zh) 作为tnf活性调节剂的稠合五环咪唑衍生物
WO1997013771A1 (en) Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors
JP2019512532A (ja) Tnf活性のモジュレーターとしての縮合六環式イミダゾール誘導体
CN115515591B (zh) 用于制备酪氨酸受体激酶抑制剂的方法
JP6483698B2 (ja) Tnf活性のモジュレーターとしてのテトラヒドロイミダゾピリジン誘導体
CN110099906A (zh) 作为激酶抑制剂的酰胺化合物
EP2968331A1 (en) Pyrimidine compounds as kinase inhibitors
EA036289B1 (ru) Конденсированные трициклические имидазопиразины в качестве ингибиторов активности tnf
US10793578B2 (en) Fused pentacyclic imidazole derivatives as modulators of TNF activity
WO2019085894A1 (zh) 一类含氮稠环化合物及其制备方法和用途
WO2025081019A1 (en) Kif modulator compounds and methods of use
WO2005061516A1 (en) Novel chemical compounds
JP7335972B2 (ja) ピペラジンアミド誘導体、その製造方法及び医薬におけるその用途
WO2018114700A1 (en) 4-amino-2-pyrido-bicyclic pyrimidines and use thereof as topoisomerase ii inhibitors
WO2011078226A1 (ja) 三環系化合物
CN117659017A (zh) Trpml1/2调节剂化合物、药物组合物及其制备方法和应用
WO2025218778A1 (zh) 杂环化合物及其作为ret抑制剂的用途

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant