MA35725B1 - Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk - Google Patents

Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk

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Publication number
MA35725B1
MA35725B1 MA37107A MA37107A MA35725B1 MA 35725 B1 MA35725 B1 MA 35725B1 MA 37107 A MA37107 A MA 37107A MA 37107 A MA37107 A MA 37107A MA 35725 B1 MA35725 B1 MA 35725B1
Authority
MA
Morocco
Prior art keywords
inhibitors
compounds
piperazine compounds
btk activity
alkylated piperazine
Prior art date
Application number
MA37107A
Other languages
English (en)
Inventor
James John Crawford
Wendy B Young
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
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of MA35725B1 publication Critical patent/MA35725B1/fr

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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
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    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-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
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
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    • 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
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    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
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Abstract

L'invention concerne des composés pipérazines alkylés de la formule i, comprenant des stéréo-isomères, des tautomères et des sels de qualité pharmaceutique de ceux-ci, lesdits composés étant utiles pour l'inhibition de la kinase btk et pour le traitement de troubles immunitaires, tels qu'une inflammation à médiation par la kinase btk. L'invention concerne également des procédés d'utilisation des composés de la formule i pour un diagnostic
MA37107A 2011-11-03 2014-06-06 Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk MA35725B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161555395P 2011-11-03 2011-11-03
PCT/US2012/063198 WO2013067277A1 (fr) 2011-11-03 2012-11-02 Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk

Publications (1)

Publication Number Publication Date
MA35725B1 true MA35725B1 (fr) 2014-12-01

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Application Number Title Priority Date Filing Date
MA37107A MA35725B1 (fr) 2011-11-03 2014-06-06 Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk

Country Status (22)

Country Link
US (3) US8729072B2 (fr)
EP (1) EP2773639B1 (fr)
JP (2) JP5976828B2 (fr)
KR (1) KR101716011B1 (fr)
CN (1) CN104024255B (fr)
AR (1) AR088642A1 (fr)
AU (1) AU2012332368A1 (fr)
BR (1) BR112014010439A2 (fr)
CA (1) CA2853970A1 (fr)
CL (1) CL2014001158A1 (fr)
CO (1) CO6950475A2 (fr)
CR (1) CR20140187A (fr)
EA (1) EA027561B1 (fr)
IL (1) IL232280A0 (fr)
IN (1) IN2014CN03265A (fr)
MA (1) MA35725B1 (fr)
MX (1) MX2014005289A (fr)
PE (1) PE20141686A1 (fr)
SG (1) SG11201401993RA (fr)
TW (1) TW201326171A (fr)
WO (1) WO2013067277A1 (fr)
ZA (1) ZA201403158B (fr)

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WO2013067277A1 (fr) * 2011-11-03 2013-05-10 Genentech, Inc. Composés pipérazines alkylés en tant qu'inhibiteurs de l'activité btk
CN105358545A (zh) 2013-07-03 2016-02-24 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
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WO2015151006A1 (fr) 2014-03-29 2015-10-08 Lupin Limited Composés de purine substitués en tant qu'inhibiteurs de btk
CN106659765B (zh) 2014-04-04 2021-08-13 德玛医药 二脱水半乳糖醇及其类似物或衍生物用于治疗非小细胞肺癌和卵巢癌的用途
WO2015170266A1 (fr) 2014-05-07 2015-11-12 Lupin Limited Composés pyrimidine substitués en tant qu'inhibiteurs de la tyrosine kinase de bruton (btk)
JP6507234B2 (ja) * 2014-10-02 2019-04-24 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft ブルトンチロシンキナーゼ(btk)によって介入される障害の処置における使用のためのピラゾールカルボキサミド化合物
CA2965178C (fr) 2014-10-22 2023-09-26 Dana-Farber Cancer Institute, Inc. Composes contenant des groupes thiazolyle pour le traitement de maladies proliferatives
CN107108604B (zh) 2014-10-27 2020-07-24 豪夫迈·罗氏有限公司 制备三环内酰胺化合物的方法
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CN114044760A (zh) * 2015-03-10 2022-02-15 奥瑞基尼探索技术有限公司 作为免疫调节剂的1,2,4-噁二唑和噻二唑化合物
CA2997859C (fr) 2016-02-29 2024-06-04 F. Hoffmann-La Roche Ag Compositions de formes galeniques comprenant un inhibiteur de la tyrosine kinase de bruton
MX2019006288A (es) 2016-12-03 2020-10-01 Juno Therapeutics Inc Metodos y composiciones para el uso de celulas t terapeuticas en combinacion con inhibidores de quinasa.
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CN107445981B (zh) * 2017-08-25 2018-06-22 牡丹江医学院 一种用于防治宫颈炎的活性化合物
CN113939292A (zh) 2019-02-25 2022-01-14 广州麓鹏制药有限公司 Btk及其突变体的抑制剂
MX2021009863A (es) 2019-03-21 2021-11-12 Onxeo Una molecula dbait en combinacion con inhibidor de quinasa para el tratamiento del cancer.
WO2021066958A1 (fr) 2019-10-05 2021-04-08 Newave Pharmaceutical Inc. Inhibiteurs de btk et leurs mutants
KR20220098759A (ko) 2019-11-08 2022-07-12 인쎄름 (엥스띠뛰 나씨오날 드 라 쌍떼 에 드 라 흐쉐르슈 메디깔) 키나제 억제제에 대해 내성을 획득한 암의 치료 방법
WO2021148581A1 (fr) 2020-01-22 2021-07-29 Onxeo Nouvelle molécule dbait et son utilisation
IL295589A (en) 2020-02-20 2022-10-01 Hutchison Medipharma Ltd The heterocyclic heteroaryl compounds and their uses
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CN116568687A (zh) 2020-09-21 2023-08-08 和记黄埔医药(上海)有限公司 杂芳基杂环化合物及其用途
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US20150094302A1 (en) 2015-04-02
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KR101716011B1 (ko) 2017-03-13
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US8946213B2 (en) 2015-02-03
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BR112014010439A2 (pt) 2017-04-18
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