PE20060421A1 - Procedimiento para preparar un compuesto de pirrolotriazina anilina como inhibidores de cinasa - Google Patents
Procedimiento para preparar un compuesto de pirrolotriazina anilina como inhibidores de cinasaInfo
- Publication number
- PE20060421A1 PE20060421A1 PE2005000918A PE2005000918A PE20060421A1 PE 20060421 A1 PE20060421 A1 PE 20060421A1 PE 2005000918 A PE2005000918 A PE 2005000918A PE 2005000918 A PE2005000918 A PE 2005000918A PE 20060421 A1 PE20060421 A1 PE 20060421A1
- Authority
- PE
- Peru
- Prior art keywords
- compound
- preparing
- procedure
- kinase inhibitors
- ester
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic 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
- C07D487/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
Abstract
SE REFIERE A UN PROCEDIMIENTO PARA PREPARAR UN COMPUESTO DE FORMULA I, DONDE R1 ES ALQUILO, ARILO INFERIOR; QUE COMPRENDE: A) PROPORCIONAR UNA MEZCLA DE UNA BASE ORGANOMETALICA FUERTE TAL COMO HEXIL LITIO O n-BUTIL LITIO Y UNA AMINA DE LA ESTRUCTURA R1NH2, DONDE R1 ES ALQUILO O ARILO INFERIOR, EN UN SOLVENTE ORGANICO; B) PROPORCIONAR UN ESTER DE ESTRUCTURA A EN UN SOLVENTE ORGANICO; C) HACER REACCIONAR LA MEZCLA DE LA ETAPA A Y EL ESTER DE LA ETAPA B PARA FORMAR EL PRODUCTO DE LA AMIDA. LA REACCION ES LLAVADA A CABO A UNA TEMPERATURA ENTRE -10°C-110°C. UN COMPUESTO EMPLEANDO DICHO PROCESO ES 4[[5-[(CICLOPROPILAMINO)CARBONIL]-2-METILFENIL]AMINO]-5-METIL-N-PROPILPIRROLO[2,1-f][1,2,4]TRIAZINA-6-CARBOXAMIDA. DICHOS COMPUESTOS SON INHIBIDORES DE p38 CINASA SIENDO UTIL EN EL TRATAMIENTO DE ARTRITIS REUMATOIDE
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60093504P | 2004-08-12 | 2004-08-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20060421A1 true PE20060421A1 (es) | 2006-06-01 |
Family
ID=35907758
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2005000918A PE20060421A1 (es) | 2004-08-12 | 2005-08-09 | Procedimiento para preparar un compuesto de pirrolotriazina anilina como inhibidores de cinasa |
Country Status (5)
Country | Link |
---|---|
US (1) | US7148348B2 (es) |
AR (1) | AR050519A1 (es) |
PE (1) | PE20060421A1 (es) |
TW (1) | TW200618803A (es) |
WO (1) | WO2006020904A1 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1992344A1 (en) | 2007-05-18 | 2008-11-19 | Institut Curie | P38 alpha as a therapeutic target in pathologies linked to FGFR3 mutation |
EP2376491B1 (en) | 2008-12-19 | 2015-03-04 | Cephalon, Inc. | Pyrrolotriazines as alk and jak2 inhibitors |
US10342786B2 (en) | 2017-10-05 | 2019-07-09 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD |
CA3128468A1 (en) | 2017-10-05 | 2019-04-11 | Fulcrum Therapeutics, Inc. | P38 kinase inhibitors reduce dux4 and downstream gene expression for the treatment of fshd |
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CA2163399A1 (en) | 1994-11-24 | 1996-05-25 | Katsuhiro Kawano | Triazine derivative, chymase activity inhibitor and nitric oxide production inhibitor |
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ATE340176T1 (de) | 1996-08-28 | 2006-10-15 | Pfizer | Substituierte 6,5-heterobicyclische-derivate |
US20010007867A1 (en) | 1999-12-13 | 2001-07-12 | Yuhpyng L. Chen | Substituted 6,5-hetero-bicyclic derivatives |
US6147080A (en) | 1996-12-18 | 2000-11-14 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
US5945418A (en) | 1996-12-18 | 1999-08-31 | Vertex Pharmaceuticals Incorporated | Inhibitors of p38 |
BR9809451A (pt) | 1997-05-22 | 2000-06-20 | Searle & Co | Pirazóis substituìdos com 3(5)-heteroarila como inibidores de quinase p38. |
US6087496A (en) | 1998-05-22 | 2000-07-11 | G. D. Searle & Co. | Substituted pyrazoles suitable as p38 kinase inhibitors |
WO1999001452A1 (en) | 1997-07-02 | 1999-01-14 | Smithkline Beecham Corporation | Novel cycloalkyl substituted imidazoles |
WO1999024033A1 (en) | 1997-11-12 | 1999-05-20 | Shionogi & Co., Ltd. | Method for the treatment of disorders associated with apoptosis using n-heterocyclic glyoxylamide compounds |
US6130235A (en) | 1998-05-22 | 2000-10-10 | Scios Inc. | Compounds and methods to treat cardiac failure and other disorders |
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IL141724A0 (en) | 1998-08-28 | 2002-03-10 | Scios Inc | INHIBITORS OF P38-α KINASE |
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GB9924092D0 (en) | 1999-10-13 | 1999-12-15 | Zeneca Ltd | Pyrimidine derivatives |
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JP2003513977A (ja) | 1999-11-10 | 2003-04-15 | オーソ−マクニール・フアーマシユーチカル・インコーポレーテツド | 置換2−アリール−3−(ヘテロアリール)−イミダゾ[1,2−α]ピリミジン類および関連薬剤組成物および方法 |
US6906067B2 (en) | 1999-12-28 | 2005-06-14 | Bristol-Myers Squibb Company | N-heterocyclic inhibitors of TNF-α expression |
US20020065270A1 (en) | 1999-12-28 | 2002-05-30 | Moriarty Kevin Joseph | N-heterocyclic inhibitors of TNF-alpha expression |
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US6670357B2 (en) | 2000-11-17 | 2003-12-30 | Bristol-Myers Squibb Company | Methods of treating p38 kinase-associated conditions and pyrrolotriazine compounds useful as kinase inhibitors |
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MY145634A (en) | 2003-12-29 | 2012-03-15 | Bristol Myers Squibb Co | Pyrrolotriazine compounds as kinase inhibitors |
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US7102002B2 (en) | 2004-06-16 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
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US7253167B2 (en) | 2004-06-30 | 2007-08-07 | Bristol-Myers Squibb Company | Tricyclic-heteroaryl compounds useful as kinase inhibitors |
TW200600513A (en) | 2004-06-30 | 2006-01-01 | Bristol Myers Squibb Co | A method for preparing pyrrolotriazine compounds |
US7102003B2 (en) | 2004-07-01 | 2006-09-05 | Bristol-Myers Squibb Company | Pyrrolotriazine compounds |
-
2005
- 2005-08-09 PE PE2005000918A patent/PE20060421A1/es not_active Application Discontinuation
- 2005-08-09 TW TW094126983A patent/TW200618803A/zh unknown
- 2005-08-09 US US11/199,746 patent/US7148348B2/en active Active
- 2005-08-11 AR ARP050103338A patent/AR050519A1/es unknown
- 2005-08-11 WO PCT/US2005/028808 patent/WO2006020904A1/en active Application Filing
Also Published As
Publication number | Publication date |
---|---|
AR050519A1 (es) | 2006-11-01 |
WO2006020904A1 (en) | 2006-02-23 |
TW200618803A (en) | 2006-06-16 |
US7148348B2 (en) | 2006-12-12 |
US20060035886A1 (en) | 2006-02-16 |
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