CL2021003057A1 - Formas cristalinas de un inhibidor btk - Google Patents

Formas cristalinas de un inhibidor btk

Info

Publication number
CL2021003057A1
CL2021003057A1 CL2021003057A CL2021003057A CL2021003057A1 CL 2021003057 A1 CL2021003057 A1 CL 2021003057A1 CL 2021003057 A CL2021003057 A CL 2021003057A CL 2021003057 A CL2021003057 A CL 2021003057A CL 2021003057 A1 CL2021003057 A1 CL 2021003057A1
Authority
CL
Chile
Prior art keywords
disorders
crystal forms
btk inhibitor
diseases
crystalline forms
Prior art date
Application number
CL2021003057A
Other languages
English (en)
Inventor
Andreas Kordikowski
Daniela Angst
Original Assignee
Novartis Ag
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 Novartis Ag filed Critical Novartis Ag
Publication of CL2021003057A1 publication Critical patent/CL2021003057A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/47One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
    • 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
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

La presente solicitud se refiere a varias formas cristalinas anhidras N–(3–(6–amino–5–(2–(N–metilacrilamido)etoxi)pirimidin–4–il)–5–fluoro–2–metilfenil)–4–ciclopropil–2–fluorobenzamida, así como composiciones, método de fabricación y sus métodos de uso. Estas formas cristalinas son útiles en el tratamiento de enfermedades y trastornos que típicamente se mejoran mediante la inhibición de BTK. Dichas enfermedades y trastornos pueden incluir trastornos inflamatorios y autoinmunes e inflamación pulmonar y del tracto respiratorio.
CL2021003057A 2019-05-23 2021-11-19 Formas cristalinas de un inhibidor btk CL2021003057A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201962851986P 2019-05-23 2019-05-23

Publications (1)

Publication Number Publication Date
CL2021003057A1 true CL2021003057A1 (es) 2022-09-09

Family

ID=70918748

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2021003057A CL2021003057A1 (es) 2019-05-23 2021-11-19 Formas cristalinas de un inhibidor btk

Country Status (13)

Country Link
EP (1) EP3972960A1 (es)
JP (1) JP2022534216A (es)
KR (1) KR20220012280A (es)
CN (1) CN113840821A (es)
AR (1) AR118981A1 (es)
AU (1) AU2020279927A1 (es)
BR (1) BR112021023054A2 (es)
CA (1) CA3137790A1 (es)
CL (1) CL2021003057A1 (es)
IL (1) IL287668A (es)
MX (1) MX2021014157A (es)
TW (1) TW202110811A (es)
WO (1) WO2020234779A1 (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022033569A1 (zh) * 2020-08-14 2022-02-17 苏州晶云药物科技股份有限公司 苯甲酰胺类化合物的晶型及其制备方法
TW202245778A (zh) 2021-01-26 2022-12-01 瑞士商諾華公司 藥物組成物
KR20240055038A (ko) 2021-09-03 2024-04-26 노파르티스 아게 다발성 경화증 치료를 위한 lou064
WO2023111802A1 (en) 2021-12-14 2023-06-22 Novartis Ag Methods of treatment using lou064
TW202342048A (zh) 2022-02-28 2023-11-01 瑞士商諾華公司 使用lou064治療化膿性汗腺炎之方法
WO2024069507A1 (en) 2022-09-30 2024-04-04 Novartis Ag Synthesis methods and intermediates for the production of remibrutinib
CN117024354B (zh) * 2023-10-08 2023-12-08 天津凯莱英制药有限公司 瑞米布替尼的制备方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NZ525656A (en) 2000-11-07 2004-12-24 Novartis Ag Indolylmaleimide derivatives as protein kinase C inhibitors
TW200918046A (en) 2002-04-03 2009-05-01 Novartis Ag Indolylmaleimide derivatives
US7365096B2 (en) 2002-12-09 2008-04-29 Board Of Regents, The University Of Texas System Methods for selectively inhibiting Janus tyrosine kinase 3 (Jak3)
PE20050158A1 (es) 2003-05-19 2005-05-12 Irm Llc Compuestos inmunosupresores y composiciones
ZA200602666B (en) 2004-01-12 2007-09-26 Cytopia Res Pty Ltd Selective kinase inhibitors
US9512084B2 (en) 2013-11-29 2016-12-06 Novartis Ag Amino pyrimidine derivatives

Also Published As

Publication number Publication date
KR20220012280A (ko) 2022-02-03
JP2022534216A (ja) 2022-07-28
IL287668A (en) 2021-12-01
EP3972960A1 (en) 2022-03-30
AU2020279927A1 (en) 2022-01-06
MX2021014157A (es) 2022-01-04
WO2020234779A1 (en) 2020-11-26
AR118981A1 (es) 2021-11-17
CA3137790A1 (en) 2020-11-26
CN113840821A (zh) 2021-12-24
TW202110811A (zh) 2021-03-16
BR112021023054A2 (pt) 2022-03-29

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