CA2916605C - Solid forms of a macrocyclic kinase inhibitor - Google Patents

Solid forms of a macrocyclic kinase inhibitor Download PDF

Info

Publication number
CA2916605C
CA2916605C CA2916605A CA2916605A CA2916605C CA 2916605 C CA2916605 C CA 2916605C CA 2916605 A CA2916605 A CA 2916605A CA 2916605 A CA2916605 A CA 2916605A CA 2916605 C CA2916605 C CA 2916605C
Authority
CA
Canada
Prior art keywords
ppm
values
crystalline
resonance
peaks
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
CA2916605A
Other languages
English (en)
French (fr)
Other versions
CA2916605A1 (en
Inventor
Andrew James Jensen
Suman Luthra
Paul Francis Richardson
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.)
Pfizer Corp SRL
Original Assignee
Pfizer Corp SRL
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 Pfizer Corp SRL filed Critical Pfizer Corp SRL
Publication of CA2916605A1 publication Critical patent/CA2916605A1/en
Application granted granted Critical
Publication of CA2916605C publication Critical patent/CA2916605C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/18Bridged systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
CA2916605A 2013-06-28 2014-06-17 Solid forms of a macrocyclic kinase inhibitor Active CA2916605C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201361840703P 2013-06-28 2013-06-28
US61/840,703 2013-06-28
PCT/IB2014/062296 WO2014207606A1 (en) 2013-06-28 2014-06-17 Solid forms of a macrocyclic kinase inhibitor

Publications (2)

Publication Number Publication Date
CA2916605A1 CA2916605A1 (en) 2014-12-31
CA2916605C true CA2916605C (en) 2018-04-24

Family

ID=51136530

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2916605A Active CA2916605C (en) 2013-06-28 2014-06-17 Solid forms of a macrocyclic kinase inhibitor

Country Status (8)

Country Link
US (1) US9637500B2 (enExample)
EP (1) EP3013835B1 (enExample)
JP (1) JP6110817B2 (enExample)
AR (1) AR096759A1 (enExample)
CA (1) CA2916605C (enExample)
ES (1) ES2656189T3 (enExample)
TW (1) TW201504246A (enExample)
WO (1) WO2014207606A1 (enExample)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016026423A1 (en) * 2014-08-20 2016-02-25 Teligene Ltd Substituted macrocycles useful as kinases inhibitors and methods of use thereof
EP3183256A4 (en) * 2014-08-20 2018-05-30 Teligene Ltd. Substituted macrocycles useful as kinases inhibitors and methods of use thereof
FI3798222T3 (fi) 2015-07-31 2023-11-28 Pfizer Lorlatinibin vapaan emäksen kidemuoto
CA3000386A1 (en) 2015-09-30 2017-04-06 Merck Patent Gmbh Combination of a pd-1 axis binding antagonist and an alk inhibitor for treating alk-negative cancer
US10543199B2 (en) 2016-03-03 2020-01-28 Shenzhen Targetrx, Inc. Macrocycle and composition comprising thereof
ES2819676T3 (es) 2016-04-08 2021-04-19 Pfizer Formas cristalinas de maleato de lorlatinib
KR102424621B1 (ko) * 2017-10-10 2022-07-25 화이자 인코포레이티드 로라티닙 유리 염기 수화물의 결정질 형태
US11179412B2 (en) 2017-12-04 2021-11-23 University of Pittsburgh—of the Commonwealth System of Higher Education Methods of treating conditions involving elevated inflammatory response
WO2019209633A1 (en) 2018-04-23 2019-10-31 Pliva Hrvatska D.O.O. Solid state forms of lorlatinib and their preparation
JP7347852B2 (ja) * 2018-11-28 2023-09-20 深▲チェン▼市塔吉瑞生物医薬有限公司 重水素化大環状化合物の調製方法
CN109651398B (zh) * 2019-01-25 2021-07-30 安庆多辉生物科技有限公司 一种合成劳拉替尼的溴代物中间体及催化合成劳拉替尼的方法
EP3999514A1 (en) * 2019-07-18 2022-05-25 Pliva Hrvatska D.O.O. Crystalline lorlatinib : fumaric acid and solid state form thereof
CN112321604A (zh) * 2019-08-05 2021-02-05 华东理工大学 大环类jak2抑制剂及其应用
CN110483551B (zh) * 2019-08-30 2021-10-22 北京赛思源生物医药技术有限公司 一种劳拉替尼游离碱的晶体
EP4041396A1 (en) 2019-10-10 2022-08-17 Sandoz AG Polymorph of lorlatinib
CN112824417A (zh) * 2019-11-21 2021-05-21 上海天慈国际药业有限公司 一种劳拉替尼的制备方法
WO2021176349A1 (en) 2020-03-05 2021-09-10 Pfizer Inc. Combination of an anaplastic lymphoma kinase inhibitor and a cyclin dependent kinase inhibitor
BR112022022530A2 (pt) 2020-05-05 2023-02-23 Nuvalent Inc Composto, composição farmacêutica, método de tratamento de câncer, método de inibição seletiva, método de redução de um nível de ros1 ou alk
CN115916754A (zh) 2020-05-05 2023-04-04 纽威伦特公司 杂芳族大环醚化学治疗剂
CN112724077B (zh) * 2020-12-29 2023-07-11 武汉利昌医药科技有限公司 一种劳拉替尼中间体的合成方法
CN113292496B (zh) * 2021-05-17 2023-03-10 安徽联创生物医药股份有限公司 一种劳拉替尼中间体的合成方法
MX2024003738A (es) 2021-10-01 2024-06-19 Nuvalent Inc Formas solidas, composiciones farmaceuticas y preparacion de compuestos de eter macrociclico heteroaromatico.

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8916593B2 (en) 2010-05-04 2014-12-23 Pfizer Inc. Alkoxy-substituted 2-aminopyridines as ALK inhibitors
WO2013132376A1 (en) 2012-03-06 2013-09-12 Pfizer Inc. Macrocyclic derivatives for the treatment of proliferative diseases

Also Published As

Publication number Publication date
EP3013835B1 (en) 2017-12-13
US20160115178A1 (en) 2016-04-28
CA2916605A1 (en) 2014-12-31
WO2014207606A1 (en) 2014-12-31
US9637500B2 (en) 2017-05-02
JP6110817B2 (ja) 2017-04-05
TW201504246A (zh) 2015-02-01
EP3013835A1 (en) 2016-05-04
ES2656189T3 (es) 2018-02-26
JP2015010091A (ja) 2015-01-19
AR096759A1 (es) 2016-02-03

Similar Documents

Publication Publication Date Title
CA2916605C (en) Solid forms of a macrocyclic kinase inhibitor
CA2937257C (en) Crystalline form of lorlatinib free base
CN113717156B (zh) Egfr抑制剂、其制备方法及用途
CN113939518B (zh) 作为激酶抑制剂的稠合三环化合物
CA3019905C (en) Crystalline forms of lorlatinib maleate
CN115611898A (zh) 四环类衍生物、其制备方法及其在医药上的应用
CN113527298B (zh) 大环内酰胺类衍生物、及其制备方法和用途
WO2025247352A1 (zh) 化合物的晶型、盐型、溶剂合物、水合物及其用途
HK40079587A (en) Crystal form of pyridazine derivative free base, and preparation method therefor and use thereof

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20151222