SI2773638T1 - Spojine heteroaril piridona in aza-priridona kot zaviralci btk-aktivnosti - Google Patents

Spojine heteroaril piridona in aza-priridona kot zaviralci btk-aktivnosti

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Publication number
SI2773638T1
SI2773638T1 SI201230367T SI201230367T SI2773638T1 SI 2773638 T1 SI2773638 T1 SI 2773638T1 SI 201230367 T SI201230367 T SI 201230367T SI 201230367 T SI201230367 T SI 201230367T SI 2773638 T1 SI2773638 T1 SI 2773638T1
Authority
SI
Slovenia
Prior art keywords
pyridone
aza
inhibitors
heteroaryl
btk activity
Prior art date
Application number
SI201230367T
Other languages
English (en)
Inventor
James John Crawford
Daniel Fred Ortwine
Binqing Wei
Wendy B. Young
Original Assignee
F. Hoffmann-La Roche 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 F. Hoffmann-La Roche Ag filed Critical F. Hoffmann-La Roche Ag
Publication of SI2773638T1 publication Critical patent/SI2773638T1/sl

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    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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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
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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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    • A61K31/495Heterocyclic 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
    • A61K31/4995Pyrazines or piperazines forming part of bridged ring systems
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    • 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
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed and containing further heterocyclic rings
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    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • 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
    • A61K31/53831,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
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    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
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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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  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
SI201230367T 2011-11-03 2012-11-02 Spojine heteroaril piridona in aza-priridona kot zaviralci btk-aktivnosti SI2773638T1 (sl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161555393P 2011-11-03 2011-11-03
PCT/US2012/063194 WO2013067274A1 (en) 2011-11-03 2012-11-02 Heteroaryl pyridone and aza-pyridone compounds as inhibitors of btk activity
EP12783837.3A EP2773638B1 (en) 2011-11-03 2012-11-02 Heteroaryl pyridone and aza-pyridone compounds as inhibitors of btk activity

Publications (1)

Publication Number Publication Date
SI2773638T1 true SI2773638T1 (sl) 2015-12-31

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Family Applications (2)

Application Number Title Priority Date Filing Date
SI201230367T SI2773638T1 (sl) 2011-11-03 2012-11-02 Spojine heteroaril piridona in aza-priridona kot zaviralci btk-aktivnosti
SI201231643T SI3002284T1 (sl) 2011-11-03 2012-11-02 Spojini heteroaril piridon in aza-piridon kot inhibitorja dejavnosti BTK

Family Applications After (1)

Application Number Title Priority Date Filing Date
SI201231643T SI3002284T1 (sl) 2011-11-03 2012-11-02 Spojini heteroaril piridon in aza-piridon kot inhibitorja dejavnosti BTK

Country Status (34)

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US (11) US8716274B2 (sl)
EP (5) EP4019508A1 (sl)
JP (5) JP5976827B2 (sl)
KR (2) KR101659193B1 (sl)
CN (2) CN107011348B (sl)
AR (2) AR088641A1 (sl)
AU (5) AU2012332365B2 (sl)
CA (1) CA2853975C (sl)
CL (1) CL2014001103A1 (sl)
CO (1) CO6950472A2 (sl)
CR (1) CR20140194A (sl)
CY (1) CY1117097T1 (sl)
DK (2) DK3002284T3 (sl)
EA (1) EA023263B1 (sl)
ES (3) ES2898938T3 (sl)
HK (1) HK1201265A1 (sl)
HR (2) HRP20151442T1 (sl)
HU (2) HUE044959T2 (sl)
IL (1) IL232060A (sl)
IN (1) IN2014CN03250A (sl)
LT (1) LT3002284T (sl)
MA (1) MA35819B1 (sl)
MX (2) MX2014005331A (sl)
PE (1) PE20141586A1 (sl)
PL (3) PL2773638T3 (sl)
PT (2) PT2773638E (sl)
RS (2) RS59016B1 (sl)
SG (1) SG11201401992YA (sl)
SI (2) SI2773638T1 (sl)
TR (1) TR201909849T4 (sl)
TW (4) TWI652270B (sl)
UA (1) UA111756C2 (sl)
WO (1) WO2013067274A1 (sl)
ZA (1) ZA201804727B (sl)

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PE20141686A1 (es) * 2011-11-03 2014-11-08 Hoffmann La Roche Compuestos de piperazina alquilados como inhibidores de actividad btk
MX2015018038A (es) * 2013-07-03 2016-03-16 Hoffmann La Roche Compuestos de heteroaril-piridona y aza-piridona-amida.
WO2015050703A1 (en) * 2013-10-04 2015-04-09 Yi Chen Inhibitors of bruton's tyrosine kinase
CA2929918C (en) * 2013-12-05 2018-01-23 F. Hoffmann-La Roche Ag Heteroaryl pyridone and aza-pyridone compounds with electrophilic functionality
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
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
CN106188063A (zh) * 2015-05-08 2016-12-07 中国科学院上海药物研究所 用作Lp-PLA2抑制剂的双环类化合物、其制备方法及医药用途
MX2018002699A (es) 2015-09-02 2018-04-13 Glaxosmithkline Ip No 2 Ltd Piridinona dicarboxamida para uso como inhibidores de bromodominio.
CA3002560A1 (en) 2015-10-23 2017-04-27 Array Biopharma, Inc. 2-aryl- and 2-heteroaryl-substituted 2-pyridazin-3(2h)-one compounds as inhibitors of fgfr tyrosine kinases
US9845325B2 (en) * 2016-02-19 2017-12-19 Novartis Ag Tetracyclic pyridone compounds as antivirals
CA2997859C (en) * 2016-02-29 2024-06-04 F. Hoffmann-La Roche Ag Dosage form compositions comprising an inhibitor of bruton's tyrosine kinase
JP6983813B2 (ja) * 2016-04-28 2021-12-17 エフ.ホフマン−ラ ロシュ アーゲーF. Hoffmann−La Roche Aktiengesellschaft 2−ピラゾロ[1,5−a]ピラジン−2−イルピリド[1,2−a]ピリミジン−4−オンの調製のためのプロセス
CN108101905A (zh) * 2016-11-24 2018-06-01 中国科学院上海药物研究所 嘧啶并[5,4-b]吲嗪或嘧啶并[5,4-b]吡呤化合物、其制备方法及用途
US11590167B2 (en) 2016-12-03 2023-02-28 Juno Therapeutic, Inc. Methods and compositions for use of therapeutic T cells in combination with kinase inhibitors
JP2020510624A (ja) 2016-12-12 2020-04-09 マルチビア インコーポレイテッド がんおよび感染性疾患の治療および予防のための、ウイルス遺伝子治療および免疫チェックポイント阻害剤を含む方法および組成物
SG10201913918UA (en) 2016-12-15 2020-03-30 Hoffmann La Roche Process for preparing btk inhibitors
CN110234652B (zh) 2016-12-22 2020-11-10 贝达药业股份有限公司 苯并咪唑衍生物及其制备方法和用途
CN110709702A (zh) * 2017-03-24 2020-01-17 豪夫迈·罗氏有限公司 治疗自身免疫性疾病和炎性疾病的方法
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