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PE20140865A1 - Inhibidores de la tirosina-quinasa de bruton - Google Patents

Inhibidores de la tirosina-quinasa de bruton

Info

Publication number
PE20140865A1
PE20140865A1 PE2014000220A PE2014000220A PE20140865A1 PE 20140865 A1 PE20140865 A1 PE 20140865A1 PE 2014000220 A PE2014000220 A PE 2014000220A PE 2014000220 A PE2014000220 A PE 2014000220A PE 20140865 A1 PE20140865 A1 PE 20140865A1
Authority
PE
Peru
Prior art keywords
methyl
pyridin
tyrosine kinase
compounds
bruton tyrosine
Prior art date
Application number
PE2014000220A
Other languages
English (en)
Inventor
Christine Brotherton-Pleiss
Saul Jaime-Figueroa
Francisco Javier Lopez-Tapia
Yan Lou
Timothy D Owens
Original Assignee
Hoffmann La Roche
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46690498&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20140865(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20140865A1 publication Critical patent/PE20140865A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Pain & Pain Management (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A COMPUESTOS HETEROCICLOS DE FORMULA (I) DONDE X ES CH, CH2, N, ENTRE OTROS; R ES H, R1, ENTRE OTROS, EN DONDE R1 ES ARILO, HETEROARILO, CICLOALQUILO, ENTRE OTROS; A, Y, Y1 E Y2 SON CADA UNO CH O N; Y3 ES H O F; Y4 ES Y4a, Y4b, ENTRE OTROS, EN DONDE Y4a ES H O HALOGENO; Y4b ES ALQUILO INFERIOR OPCIONALMENTE SUSTITUIDO CON HALOGENO, HIDROXI, CN, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: 6-TERT-BUTIL-8-FLUOR-2-{3-HIDROXIMETIL-4-[1-METIL-5-(1'-METIL-1',2',3',4',5',6'-HEXAHIDRO-[3,4']BIPIRIDINIL-6-ILAMINO)-6-OXO-1,6-DIHIDRO-PIRIDAZIN-3-IL]-PIRIDIN-2-IL}-2H-FTALAZIN-1-ONA; 6-TERT-BUTIL-8-FLUOR-2-(3-HIDROXIMETIL-4-{1-METIL-5-[5-((S)-1-METIL-PIRROLIDIN-2-IL)-PIRIDIN-2-ILAMINO]-6-OXO-1,6-DIHIDRO-PIRIDAZIN-3-IL}-PIRIDIN-2-IL)-2H-FTALAZIN-1-ONA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA TIROSINA QUINASA DE BRUTON (BTK) SIENDO UTILES EN EL TRATAMIENTO DE ARTRITIS REUMATOIDE, ASMA
PE2014000220A 2011-08-17 2012-08-14 Inhibidores de la tirosina-quinasa de bruton PE20140865A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161524374P 2011-08-17 2011-08-17
US201261649991P 2012-05-22 2012-05-22

Publications (1)

Publication Number Publication Date
PE20140865A1 true PE20140865A1 (es) 2014-07-19

Family

ID=46690498

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2014000220A PE20140865A1 (es) 2011-08-17 2012-08-14 Inhibidores de la tirosina-quinasa de bruton

Country Status (23)

Country Link
US (1) US8889682B2 (es)
EP (1) EP2744804B1 (es)
JP (1) JP5823616B2 (es)
KR (1) KR20140052032A (es)
CN (1) CN103748088A (es)
AR (1) AR087543A1 (es)
AU (1) AU2012296888A1 (es)
BR (1) BR112014003582A2 (es)
CA (1) CA2841801A1 (es)
CL (1) CL2014000350A1 (es)
CO (1) CO6842020A2 (es)
CR (1) CR20140027A (es)
EA (1) EA024689B1 (es)
EC (1) ECSP14013212A (es)
HK (1) HK1197060A1 (es)
IL (1) IL230561A0 (es)
MA (1) MA35419B1 (es)
MX (1) MX349372B (es)
PE (1) PE20140865A1 (es)
PH (1) PH12014500128A1 (es)
TW (1) TW201311669A (es)
WO (1) WO2013024078A1 (es)
ZA (1) ZA201400739B (es)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013067277A1 (en) 2011-11-03 2013-05-10 Genentech, Inc. Alkylated piperazine compounds as inhibitors of btk activity
EP2773632B1 (en) * 2011-11-03 2017-04-12 F. Hoffmann-La Roche AG 8-fluorophthalazin-1(2h)-one compounds as inhibitors of btk activity
CN104105697B (zh) 2011-11-03 2016-11-09 霍夫曼-拉罗奇有限公司 二环哌嗪化合物
UA111756C2 (uk) 2011-11-03 2016-06-10 Ф. Хоффманн-Ля Рош Аг Сполуки гетероарилпіридону та азапіридону як інгібітори тирозинкінази брутона
WO2013157021A1 (en) 2012-04-20 2013-10-24 Advinus Therapeutics Limited Bicyclic compounds, compositions and medicinal applications thereof
CA2869954C (en) 2012-04-20 2023-01-03 Advinus Therapeutics Limited Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof in medical conditions related to modulation of bruton's tyrosine kinase activity
EP3550031A1 (en) 2012-07-24 2019-10-09 Pharmacyclics, LLC Mutations associated with resistance to inhibitors of bruton's tyrosine kinase (btk)
BR112015002590A2 (pt) 2012-08-10 2019-08-06 Boehringer Ingelheim Int compostos heteroaromáticos como inibidores de tirosina cinase de bruton (btk)
MX2015006162A (es) * 2012-11-16 2015-08-14 Hoffmann La Roche Inhibidores de la tirosina-cinasa de bruton.
KR20150075115A (ko) * 2012-11-30 2015-07-02 에프. 호프만-라 로슈 아게 브루톤 티로신 키나제의 억제제
KR101737724B1 (ko) 2013-03-05 2017-05-29 에프. 호프만-라 로슈 아게 브루톤 티로신 키나아제의 억제제
CN104177338B (zh) * 2013-05-22 2018-04-03 南京勇山生物科技有限公司 一类布鲁顿激酶抑制剂
HK1214820A1 (zh) * 2013-07-03 2016-08-05 豪夫迈.罗氏有限公司 杂芳基吡啶酮和氮杂-吡啶酮酰胺化合物
WO2015012149A1 (ja) 2013-07-26 2015-01-29 カルナバイオサイエンス株式会社 新規トリアジン誘導体
AU2014322239A1 (en) * 2013-09-20 2016-04-14 Carna Biosciences, Inc. Novel triazine derivative
WO2015082583A1 (en) 2013-12-05 2015-06-11 F. Hoffmann-La Roche Ag Heteroaryl pyridone and aza-pyridone compounds with electrophilic functionality
EP3042903B1 (en) 2015-01-06 2019-08-14 Impetis Biosciences Ltd. Substituted hetero-bicyclic compounds, compositions and medicinal applications thereof
ES2738630T3 (es) 2015-01-22 2020-01-24 Sanofi Aventis Deutschland Procedimiento para la producción de 2-[4-(ciclopropanocarbonil)fenil]-2-metil-propanonitrilo
EP3365335B1 (en) 2015-10-23 2024-02-14 Array Biopharma, Inc. 2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases
EP3877371A4 (en) 2018-11-07 2022-07-27 Dana-Farber Cancer Institute, Inc. IMIDAZOPYRIDINE DERIVATIVES AND AZA-IMIDAZOPYRIDINE DERIVATIVES AS JANUS KINASE 2 INHIBITORS AND USES THEREOF
EP3876939A4 (en) 2018-11-07 2022-08-10 Dana-Farber Cancer Institute, Inc. Benzothiazole derivatives and 7-aza-benzothiazole derivatives as janus kinase 2 inhibitors and uses thereof
WO2020097396A1 (en) 2018-11-07 2020-05-14 Dana-Farber Cancer Institute, Inc. Benzimidazole derivatives and aza-benzimidazole derivatives as janus kinase 2 inhibitors and uses thereof
JP2022515198A (ja) 2018-12-19 2022-02-17 アレイ バイオファーマ インコーポレイテッド FGFRチロシンキナーゼの阻害剤としての置換ピラゾロ[1,5-a]ピリジン化合物
WO2020131674A1 (en) 2018-12-19 2020-06-25 Array Biopharma Inc. 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer
CN115996917B (zh) 2020-05-06 2025-10-28 艾捷斯治疗公司 作为jak2抑制剂的6-杂芳基氧基苯并咪唑和氮杂苯并咪唑
US12043632B2 (en) 2020-12-23 2024-07-23 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles and azabenzimidazoles as JAK2 inhibitors
WO2023009709A1 (en) * 2021-07-29 2023-02-02 Ajax Therapeutics, Inc. Pyrazolo piperazines as jak2 inhibitors
CA3234638A1 (en) 2021-11-09 2023-05-19 Ajax Therapeutics, Inc. 6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors
TW202325289A (zh) 2021-11-09 2023-07-01 美商雅捷可斯治療公司 Jak2抑制劑之形式及組合物
CN115073299B (zh) * 2022-06-14 2024-06-25 爱斯特(成都)生物制药股份有限公司 一种制备2-氟-3-三氟甲基苯胺的方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7683064B2 (en) * 2008-02-05 2010-03-23 Roche Palo Alto Llc Inhibitors of Bruton's tyrosine kinase
MY158411A (en) * 2008-02-05 2016-10-14 Hoffmann La Roche Novel pyridinones and pyridazinones
WO2009156284A1 (en) 2008-06-24 2009-12-30 F. Hoffmann-La Roche Ag Novel substituted pyridin-2-ones and pyridazin-3-ones
US8299077B2 (en) * 2009-03-02 2012-10-30 Roche Palo Alto Llc Inhibitors of Bruton's tyrosine kinase
AR082590A1 (es) * 2010-08-12 2012-12-19 Hoffmann La Roche Inhibidores de la tirosina-quinasa de bruton
EP2773632B1 (en) * 2011-11-03 2017-04-12 F. Hoffmann-La Roche AG 8-fluorophthalazin-1(2h)-one compounds as inhibitors of btk activity
EP2788020A4 (en) * 2011-12-05 2015-04-29 Immunomedics Inc THERAPEUTIC USE OF ANTI-CD22 ANTIBODIES FOR THE INDUCTION OF TROGO CYTOSIS

Also Published As

Publication number Publication date
CO6842020A2 (es) 2014-01-20
WO2013024078A1 (en) 2013-02-21
MX2014001653A (es) 2014-03-21
BR112014003582A2 (pt) 2017-03-14
EA201490452A1 (ru) 2014-05-30
JP2014521734A (ja) 2014-08-28
EP2744804B1 (en) 2017-05-17
CR20140027A (es) 2014-03-13
EA024689B1 (ru) 2016-10-31
CN103748088A (zh) 2014-04-23
AR087543A1 (es) 2014-04-03
JP5823616B2 (ja) 2015-11-25
US20130045965A1 (en) 2013-02-21
CA2841801A1 (en) 2013-02-21
KR20140052032A (ko) 2014-05-02
TW201311669A (zh) 2013-03-16
ECSP14013212A (es) 2014-03-31
CL2014000350A1 (es) 2014-08-22
ZA201400739B (en) 2016-01-27
EP2744804A1 (en) 2014-06-25
MA35419B1 (fr) 2014-09-01
MX349372B (es) 2017-07-26
AU2012296888A1 (en) 2014-01-23
IL230561A0 (en) 2014-03-31
HK1197060A1 (en) 2015-01-02
PH12014500128A1 (en) 2014-02-24
US8889682B2 (en) 2014-11-18

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