MX2014005282A - Compuestos de 8-fluoroftalazin-1 (2h) -ona. - Google Patents

Compuestos de 8-fluoroftalazin-1 (2h) -ona.

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Publication number
MX2014005282A
MX2014005282A MX2014005282A MX2014005282A MX2014005282A MX 2014005282 A MX2014005282 A MX 2014005282A MX 2014005282 A MX2014005282 A MX 2014005282A MX 2014005282 A MX2014005282 A MX 2014005282A MX 2014005282 A MX2014005282 A MX 2014005282A
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MX
Mexico
Prior art keywords
compounds
fluorophthalazin
inhibitors
btk activity
formula
Prior art date
Application number
MX2014005282A
Other languages
English (en)
Inventor
Binqing Wei
Daniel Fred Ortwine
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 MX2014005282A publication Critical patent/MX2014005282A/es

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    • 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
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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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/502Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
    • AHUMAN NECESSITIES
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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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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    • A61K31/33Heterocyclic compounds
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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
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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    • A61K31/33Heterocyclic compounds
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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
    • A61K31/53831,4-Oxazines, e.g. morpholine ortho- or peri-condensed with heterocyclic ring systems
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    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

Se proporcionan compuestos de 8-fluoroftalazin- 1(2h)-ona de la fórmula II en donde uno o dos de X1, X2 y X3 son N, incluyendo estereoisómeros, tautómeros y sales farmacéuticamente aceptables de los mismos, útiles para inhibir la Btk quinasa y para el tratamiento de trastornos del sistema inmune tales como inflamación mediada por Btk quinasa. Se describen métodos para utilizar compuestos de la Fórmula II para diagnóstico y tratamiento in vitro, in situ e in vivo de estos trastornos en células de mamíferos, o condiciones patológicas asociadas. (ver Fórmula).
MX2014005282A 2011-11-03 2012-11-02 Compuestos de 8-fluoroftalazin-1 (2h) -ona. MX2014005282A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161555398P 2011-11-03 2011-11-03
PCT/US2012/063177 WO2013067264A1 (en) 2011-11-03 2012-11-02 8-fluorophthalazin-1 (2h) - one compounds as inhibitors of btk activity

Publications (1)

Publication Number Publication Date
MX2014005282A true MX2014005282A (es) 2014-05-30

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MX2014005282A MX2014005282A (es) 2011-11-03 2012-11-02 Compuestos de 8-fluoroftalazin-1 (2h) -ona.

Country Status (13)

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US (2) US8669251B2 (es)
EP (1) EP2773632B1 (es)
JP (2) JP5976826B2 (es)
KR (1) KR101696525B1 (es)
CN (1) CN104203937A (es)
AR (1) AR088643A1 (es)
BR (1) BR112014010460A2 (es)
CA (1) CA2853967A1 (es)
HK (1) HK1205111A1 (es)
MX (1) MX2014005282A (es)
RU (1) RU2622391C2 (es)
TW (1) TWI553004B (es)
WO (1) WO2013067264A1 (es)

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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
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RU2622391C2 (ru) 2017-06-15
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CA2853967A1 (en) 2013-05-10
EP2773632A1 (en) 2014-09-10
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CN104203937A (zh) 2014-12-10
BR112014010460A2 (pt) 2017-04-18
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EP2773632B1 (en) 2017-04-12
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US8669251B2 (en) 2014-03-11
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US8754077B2 (en) 2014-06-17
WO2013067264A1 (en) 2013-05-10

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