ES2950569T3 - (S)-4-(8-amino-3-(1-(but-2-inoil)pirrolidin-2-il)imidazo[1,5-a]pirazin-1-il)-2-metoxi-n-(piridin-2-il)benzamida como inhibidor de la Btk - Google Patents

(S)-4-(8-amino-3-(1-(but-2-inoil)pirrolidin-2-il)imidazo[1,5-a]pirazin-1-il)-2-metoxi-n-(piridin-2-il)benzamida como inhibidor de la Btk Download PDF

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Publication number
ES2950569T3
ES2950569T3 ES18203086T ES18203086T ES2950569T3 ES 2950569 T3 ES2950569 T3 ES 2950569T3 ES 18203086 T ES18203086 T ES 18203086T ES 18203086 T ES18203086 T ES 18203086T ES 2950569 T3 ES2950569 T3 ES 2950569T3
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Spain
Prior art keywords
compound
disease
benzamide
btk
amino
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Active
Application number
ES18203086T
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English (en)
Spanish (es)
Inventor
Tjeerd A Barf
Christiaan Geradus Johannes Maria Jans
Man Adrianus Petrus Antonius De
Arthur A Oubrie
Hans C A Raaijmakers
Johannes Bernardus Maria Rewinkel
Jan-Gerard Sterrenburg
Jacobus C H M Wijkmans
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Organon Pharma UK Ltd
Merck Sharp and Dohme BV
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Merck Sharp and Dohme Ltd
Merck Sharp and Dohme BV
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Application filed by Merck Sharp and Dohme Ltd, Merck Sharp and Dohme BV filed Critical Merck Sharp and Dohme Ltd
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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
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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
    • A61K31/4985Pyrazines 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
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    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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ES18203086T 2011-07-19 2012-07-11 (S)-4-(8-amino-3-(1-(but-2-inoil)pirrolidin-2-il)imidazo[1,5-a]pirazin-1-il)-2-metoxi-n-(piridin-2-il)benzamida como inhibidor de la Btk Active ES2950569T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161509397P 2011-07-19 2011-07-19
EP11174578 2011-07-19

Publications (1)

Publication Number Publication Date
ES2950569T3 true ES2950569T3 (es) 2023-10-11

Family

ID=47557677

Family Applications (3)

Application Number Title Priority Date Filing Date
ES19215783T Active ES2904707T3 (es) 2011-07-19 2012-07-11 4-imidazopiridazin-1-il-benzamidas y 4-imidazotriazin-1-il-benzamidas como inhibidores de Btk
ES12733505T Active ES2708224T3 (es) 2011-07-19 2012-07-11 4-Imidazopiridazín-1-il-benzamidas y 4-imidazotriazín-1-il-benzamidas como inhibidores de Btk
ES18203086T Active ES2950569T3 (es) 2011-07-19 2012-07-11 (S)-4-(8-amino-3-(1-(but-2-inoil)pirrolidin-2-il)imidazo[1,5-a]pirazin-1-il)-2-metoxi-n-(piridin-2-il)benzamida como inhibidor de la Btk

Family Applications Before (2)

Application Number Title Priority Date Filing Date
ES19215783T Active ES2904707T3 (es) 2011-07-19 2012-07-11 4-imidazopiridazin-1-il-benzamidas y 4-imidazotriazin-1-il-benzamidas como inhibidores de Btk
ES12733505T Active ES2708224T3 (es) 2011-07-19 2012-07-11 4-Imidazopiridazín-1-il-benzamidas y 4-imidazotriazín-1-il-benzamidas como inhibidores de Btk

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US (7) US9290504B2 (enExample)
EP (4) EP2734522B1 (enExample)
JP (6) JP5826931B2 (enExample)
KR (2) KR101802689B1 (enExample)
CN (2) CN103889987B (enExample)
AU (4) AU2012285987C1 (enExample)
BR (1) BR112014001255B1 (enExample)
CA (1) CA2841886C (enExample)
CL (1) CL2014000130A1 (enExample)
CO (1) CO6940411A2 (enExample)
CR (1) CR20140030A (enExample)
CY (2) CY2021010I2 (enExample)
DK (2) DK3689878T3 (enExample)
DO (1) DOP2014000008A (enExample)
EA (2) EA037644B1 (enExample)
EC (1) ECSP14013217A (enExample)
ES (3) ES2904707T3 (enExample)
GT (1) GT201400009A (enExample)
HR (2) HRP20212021T1 (enExample)
HU (3) HUE041987T2 (enExample)
IL (3) IL230511B (enExample)
IN (1) IN2014CN00408A (enExample)
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MY (1) MY192354A (enExample)
PE (1) PE20141681A1 (enExample)
PH (2) PH12014500148A1 (enExample)
PL (2) PL3689878T3 (enExample)
PT (1) PT3689878T (enExample)
RS (2) RS62760B1 (enExample)
SG (1) SG10201605913VA (enExample)
SI (2) SI3689878T1 (enExample)
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TN (1) TN2014000027A1 (enExample)
UA (1) UA115312C2 (enExample)
WO (1) WO2013010868A1 (enExample)
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MX342405B (es) 2010-06-03 2016-09-28 Pharmacyclics Inc El uso de inhibidores de la tirosina quinasa de bruton (btk).
CN103534258B (zh) 2011-05-17 2016-09-14 普林斯匹亚生物制药公司 酪氨酸激酶抑制剂
US9376438B2 (en) 2011-05-17 2016-06-28 Principia Biopharma, Inc. Pyrazolopyrimidine derivatives as tyrosine kinase inhibitors
CN103857396A (zh) 2011-07-13 2014-06-11 药品循环公司 布鲁顿酪氨酸激酶抑制剂
SI3689878T1 (sl) 2011-07-19 2021-12-31 Merck Sharp & Dohme B.V. 4-imidazopiridazin-1-il-benzamidi in 4-imidazotriazin-1-il-benzamidi kot Btk-zaviralci
EP2548877A1 (en) 2011-07-19 2013-01-23 MSD Oss B.V. 4-(5-Membered fused pyridinyl)benzamides as BTK-inhibitors
BR112015001690A2 (pt) 2012-07-24 2017-11-07 Pharmacyclics Inc mutações associadas com a resistência a inibidores da tirosina quinase de bruton (btk)
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