BRPI0514865A - processo para preparar um composto - Google Patents
processo para preparar um compostoInfo
- Publication number
- BRPI0514865A BRPI0514865A BRPI0514865-0A BRPI0514865A BRPI0514865A BR PI0514865 A BRPI0514865 A BR PI0514865A BR PI0514865 A BRPI0514865 A BR PI0514865A BR PI0514865 A BRPI0514865 A BR PI0514865A
- Authority
- BR
- Brazil
- Prior art keywords
- oxo
- preparing
- compound
- indolines
- dioxo
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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 two hetero rings
- C07D401/04—Heterocyclic 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 two hetero rings directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
- A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Immunology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Transplantation (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PROCESSO PARA PREPARAR UM COMPOSTO A presente invenção refere-se aos processos novos para a preparação de 2-(2,6-dioxo-piperidin-3-il)-1-oxo-indolinas substituídas que são úteis para a prevenção ou o tratamento de doenças ou condições relacionadas com uma atividade ou nível anormalmente alto de TNF<244>. A invenção proporciona processos para a produção comercial de 2-(2,6-dioxo-piperidin-3-il)-1-oxo-indolinas substituídas incluindo, mas não limitado a, 3-(4-amino-1-oxo-isoindolin-2-il)-piperidina-2,6-diona terapeuticamente ativa.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US60740904P | 2004-09-03 | 2004-09-03 | |
PCT/US2005/031318 WO2006028964A1 (en) | 2004-09-03 | 2005-08-31 | Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines |
Publications (1)
Publication Number | Publication Date |
---|---|
BRPI0514865A true BRPI0514865A (pt) | 2008-06-24 |
Family
ID=35385616
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
BRPI0514865-0A BRPI0514865A (pt) | 2004-09-03 | 2005-08-31 | processo para preparar um composto |
Country Status (22)
Country | Link |
---|---|
US (1) | US7863451B2 (pt) |
EP (2) | EP2479172B1 (pt) |
JP (2) | JP2008512379A (pt) |
KR (1) | KR20070057907A (pt) |
CN (1) | CN101080400A (pt) |
AR (1) | AR050724A1 (pt) |
AU (1) | AU2005282728A1 (pt) |
BR (1) | BRPI0514865A (pt) |
CA (1) | CA2579291C (pt) |
ES (2) | ES2437592T3 (pt) |
GT (1) | GT200500242A (pt) |
HN (1) | HN2005000508A (pt) |
IL (1) | IL181674A0 (pt) |
MX (1) | MX2007002521A (pt) |
NZ (1) | NZ554068A (pt) |
PA (1) | PA8643901A1 (pt) |
PE (1) | PE20060648A1 (pt) |
SV (1) | SV2007002219A (pt) |
TW (1) | TW200621748A (pt) |
UY (1) | UY29097A1 (pt) |
WO (1) | WO2006028964A1 (pt) |
ZA (1) | ZA200702382B (pt) |
Families Citing this family (41)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7629360B2 (en) * | 1999-05-07 | 2009-12-08 | Celgene Corporation | Methods for the treatment of cachexia and graft v. host disease |
US7323479B2 (en) * | 2002-05-17 | 2008-01-29 | Celgene Corporation | Methods for treatment and management of brain cancer using 1-oxo-2-(2,6-dioxopiperidin-3-yl)-4-methylisoindoline |
UA83504C2 (en) | 2003-09-04 | 2008-07-25 | Селджин Корпорейшн | Polymorphic forms of 3-(4-amino-1-oxo-1,3 dihydro-isoindol-2-yl)-piperidine-2,6-dione |
ES2430545T3 (es) | 2005-06-30 | 2013-11-21 | Celgene Corporation | Procedimientos para la preparación de compuestos de 4-amino-2-(2,6-dioxopiperidin-3-il)isoindolina-1,3-diona |
CN101186611B (zh) * | 2006-11-15 | 2011-05-18 | 天津和美生物技术有限公司 | 可抑制细胞释放肿瘤坏死因子的吡咯啉-2-酮衍生物及其制备和应用 |
CN101959856A (zh) * | 2008-03-11 | 2011-01-26 | 雷迪博士实验室有限公司 | 来那度胺的制备 |
DE102008057335A1 (de) | 2008-11-14 | 2010-05-20 | Ratiopharm Gmbh | Amorphes Lenalidomid |
DE102008057284A1 (de) | 2008-11-14 | 2010-05-20 | Ratiopharm Gmbh | Tabletten enthaltend Lenalidomid und Adhäsionsverstärker |
DE102008057285A1 (de) | 2008-11-14 | 2010-05-20 | Ratiopharm Gmbh | 3-(4-Amino-1,3-dihydro-1-oxo-2H-isoindol-2-yl)-2,6-piperidindion in Form einer festen Lösung |
WO2010056384A1 (en) * | 2008-11-17 | 2010-05-20 | Dr. Reddy's Laboratories Ltd. | Lenalidomide solvates and processes |
WO2010093434A1 (en) | 2009-02-11 | 2010-08-19 | Celgene Corporation | Isotopologues of lenalidomide |
US8946265B2 (en) * | 2009-03-02 | 2015-02-03 | Generics [Uk] Limited | Process for the preparation of lenalidomide |
CN101580501B (zh) * | 2009-06-01 | 2011-03-09 | 南京卡文迪许生物工程技术有限公司 | 3-(取代二氢异吲哚酮-2-基)-2,6-哌啶二酮的合成方法及其中间体 |
AU2009350978A1 (en) * | 2009-08-12 | 2012-04-05 | Synthon B.V. | Lenalidomide salts |
PL2477973T3 (pl) * | 2009-09-16 | 2015-04-30 | Ranbaxy Laboratories Ltd | Sposób wytwarzania krystalicznej formy lenalidomidu |
TWI475014B (zh) * | 2009-09-17 | 2015-03-01 | Scinopharm Taiwan Ltd | 固體形態的3-(4-胺基-1-側氧基-1,3-二氫-異吲哚-2-基)-哌啶-2,6-二酮及其製造方法 |
WO2011050962A1 (en) | 2009-10-29 | 2011-05-05 | Ratiopharm Gmbh | Acid addition salts of lenalidomide |
CN102060842B (zh) * | 2009-11-02 | 2013-05-08 | 南京卡文迪许生物工程技术有限公司 | 3-(取代二氢异吲哚-2-基)-2,6-哌啶二酮多晶型物和药用组合物 |
CN101696205B (zh) | 2009-11-02 | 2011-10-19 | 南京卡文迪许生物工程技术有限公司 | 3-(取代二氢异吲哚-2-基)-2,6-哌啶二酮多晶型物和药用组合物 |
CN102127054B (zh) * | 2009-11-02 | 2013-04-03 | 南京卡文迪许生物工程技术有限公司 | 3-(取代二氢异吲哚-2-基)-2,6-哌啶二酮多晶型物和药用组合物 |
WO2011069608A1 (en) * | 2009-12-09 | 2011-06-16 | Ratiopharm Gmbh | S-lenalidomide, polymorphic forms thereof and blend comprising s- und r-lenalidomide |
CN101817813B (zh) * | 2010-01-15 | 2013-04-10 | 南京卡文迪许生物工程技术有限公司 | 3-(取代二氢异吲哚酮-2-基)-2,6-哌啶二酮晶体ⅳ及其药用组合物 |
SI3202461T1 (sl) | 2010-02-11 | 2019-05-31 | Celgene Corporation | Derivati arilmetoksi izoindolina in sestavki, ki jih vsebujejo in metode uporabe le teh |
CN102453021A (zh) * | 2010-10-22 | 2012-05-16 | 重庆医药工业研究院有限责任公司 | 来那度胺的新晶型及其制备方法 |
WO2012079075A1 (en) | 2010-12-10 | 2012-06-14 | Concert Pharmaceuticals, Inc. | Deuterated phthalimide derivatives |
CA2842316A1 (en) | 2011-07-19 | 2013-01-24 | Amplio Pharma, Llc | Urea cocrystal of 3-(4-amin0-1-0x0-1,3 dihydro-isoindol-2-yl)piperidine-2,6-dione |
US9133161B2 (en) * | 2012-07-27 | 2015-09-15 | Celgene Corporation | Processes for preparing isoindoline-1,3-dione compounds |
CA2879151C (en) * | 2012-08-09 | 2021-03-30 | Celgene Corporation | Processes for the preparation of (s)-3-(4-((4-(morpholinomethyl)benzyl)oxy)-1-oxoisoindolin-2-yl)piperidine-2,6-dione and pharmaceutically acceptable forms thereof |
WO2014110322A2 (en) | 2013-01-11 | 2014-07-17 | Concert Pharmaceuticals, Inc. | Substituted dioxopiperidinyl phthalimide derivatives |
CN103242215A (zh) * | 2013-05-27 | 2013-08-14 | 合肥医工医药有限公司 | 一种来那度胺中间体的制备方法 |
US10392364B2 (en) | 2014-08-11 | 2019-08-27 | Avra Laboratories Pvt. Ltd. | Process for synthesis of lenalidomide |
KR102191256B1 (ko) | 2014-10-30 | 2020-12-15 | 강푸 바이오파마슈티칼즈 리미티드 | 이소인돌린 유도체, 이의 중간체, 제조방법, 약물 조성물 및 응용 |
CN104447689B (zh) * | 2014-12-22 | 2016-07-20 | 上海迈柏医药科技有限公司 | 来那度胺的晶型及其制备方法 |
TWI793151B (zh) * | 2017-08-23 | 2023-02-21 | 瑞士商諾華公司 | 3-(1-氧異吲哚啉-2-基)之氫吡啶-2,6-二酮衍生物及其用途 |
CN108191826A (zh) * | 2018-01-08 | 2018-06-22 | 浙江省医学科学院 | 一种来那度胺晶体及其制备方法 |
WO2019209692A1 (en) | 2018-04-23 | 2019-10-31 | Celgene Corporation | Substituted 4-aminoisoindoline-1,3-dione compounds and their use for treating lymphoma |
AR116109A1 (es) | 2018-07-10 | 2021-03-31 | Novartis Ag | Derivados de 3-(5-amino-1-oxoisoindolin-2-il)piperidina-2,6-diona y usos de los mismos |
JOP20210001A1 (ar) | 2018-07-10 | 2021-01-05 | Novartis Ag | مشتقات 3-(5- هيدروكسي -1- أوكسو أيزو إندولين -2- يل) بيبريدين -2، 6- دايون واستخدامها لمعالجة أمراض مرتبطة ببروتين ذات أصبع الزنك من عائلة (ikaros 2 (ikzf2 |
JP7098825B2 (ja) * | 2018-09-07 | 2022-07-11 | メッドシャイン ディスカバリー インコーポレイテッド | 三環式置換ピペリジンジオン類化合物 |
AU2019381688A1 (en) | 2018-11-13 | 2021-06-03 | Biotheryx, Inc. | Substituted isoindolinones |
CN109369504B (zh) * | 2018-12-06 | 2020-05-12 | 温州大学 | 含硫3-亚甲基异吲哚啉-1-酮衍生物的制备方法 |
Family Cites Families (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR0166088B1 (ko) * | 1990-01-23 | 1999-01-15 | . | 수용해도가 증가된 시클로덱스트린 유도체 및 이의 용도 |
DE4236880A1 (de) * | 1992-10-31 | 1994-05-05 | Basf Ag | N-Phenyl substituierte Glutarimide und N-Phenylglutarsäureamide, deren Herstellung und Verwendung |
US6114355A (en) | 1993-03-01 | 2000-09-05 | D'amato; Robert | Methods and compositions for inhibition of angiogenesis |
US5629327A (en) * | 1993-03-01 | 1997-05-13 | Childrens Hospital Medical Center Corp. | Methods and compositions for inhibition of angiogenesis |
US5463063A (en) * | 1993-07-02 | 1995-10-31 | Celgene Corporation | Ring closure of N-phthaloylglutamines |
US5698579A (en) * | 1993-07-02 | 1997-12-16 | Celgene Corporation | Cyclic amides |
DE19601303A1 (de) * | 1996-01-16 | 1997-07-17 | Boehringer Ingelheim Kg | Neuartige Benzoylguanidin-Derivate, Verfahren zu ihrer Herstellung und ihre Verwendung bei der Herstellung von Arzneimitteln |
US5635517B1 (en) * | 1996-07-24 | 1999-06-29 | Celgene Corp | Method of reducing TNFalpha levels with amino substituted 2-(2,6-dioxopiperidin-3-YL)-1-oxo-and 1,3-dioxoisoindolines |
HU228769B1 (en) * | 1996-07-24 | 2013-05-28 | Celgene Corp | Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha |
CZ304569B6 (cs) * | 1996-07-24 | 2014-07-09 | Celgene Corporation | 1,3-Dioxo-2-(2,6-dioxopiperidin-3-yl)-4-aminoisoindolin pro použití pro snížení nežádoucí hladiny TNFα u savce |
US5798368A (en) * | 1996-08-22 | 1998-08-25 | Celgene Corporation | Tetrasubstituted 2-(2,6-dioxopiperidin-3-yl)-1-oxoisoindolines and method of reducing TNFα levels |
US6281230B1 (en) * | 1996-07-24 | 2001-08-28 | Celgene Corporation | Isoindolines, method of use, and pharmaceutical compositions |
CZ299810B6 (cs) * | 1996-08-12 | 2008-12-03 | Celgene Corporation | Substituovaná aromatická sloucenina a její použití pro snížení hladiny cytokinu |
US5874448A (en) * | 1997-11-18 | 1999-02-23 | Celgene Corporation | Substituted 2-(2,6 dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing TNFα levels |
US5955476A (en) * | 1997-11-18 | 1999-09-21 | Celgene Corporation | Substituted 2-(2,6-dioxo-3-fluoropiperidin-3-yl)-isoindolines and method of reducing inflammatory cytokine levels |
TR200101500T2 (tr) * | 1998-03-16 | 2002-06-21 | Celgene Corporation | 2-(2,6-dioksopiperidin-3-il)izoindolin türevleri, bunların hazırlanması ve enflamatuarn sitokinlerin inhibitörleri olarak kullanımı. |
DE60023123T2 (de) * | 1999-03-18 | 2006-06-22 | Celgene Corp. | Substituierte 1-oxo- und 1,3-dioxoisoindoline und ihre verwendung in pharmazeutischen zusammensetzungen zur senkung des spiegels inflammatorisch wirkender cytokine |
EP1193248A1 (en) * | 2000-09-30 | 2002-04-03 | Aventis Pharma Deutschland GmbH | Malonamid and malonamic ester derivatives with antithrombotic activity, their preparation and their use |
US6458810B1 (en) * | 2000-11-14 | 2002-10-01 | George Muller | Pharmaceutically active isoindoline derivatives |
DK1353672T3 (da) * | 2000-11-30 | 2008-01-21 | Childrens Medical Center | Syntese af 4-amino-thalidomidenantiomerer |
US20030045552A1 (en) * | 2000-12-27 | 2003-03-06 | Robarge Michael J. | Isoindole-imide compounds, compositions, and uses thereof |
US7091353B2 (en) * | 2000-12-27 | 2006-08-15 | Celgene Corporation | Isoindole-imide compounds, compositions, and uses thereof |
JP2002284761A (ja) * | 2001-01-17 | 2002-10-03 | Toray Ind Inc | 光学活性3−アミノピロリジン−2,5−ジオン誘導体および光学活性3−アミノピロリジン誘導体の製造方法 |
ATE428419T1 (de) * | 2001-08-06 | 2009-05-15 | Childrens Medical Center | Antiangiogenese wirkung von stickstoffsubstituierten thalidomid-analoga |
EP1485100B1 (en) * | 2002-03-15 | 2010-05-05 | Vertex Pharmaceuticals Incorporated | Azinylaminoazoles as inhibitors of protein kinases |
US7968569B2 (en) * | 2002-05-17 | 2011-06-28 | Celgene Corporation | Methods for treatment of multiple myeloma using 3-(4-amino-1-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione |
US7189740B2 (en) * | 2002-10-15 | 2007-03-13 | Celgene Corporation | Methods of using 3-(4-amino-oxo-1,3-dihydro-isoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myelodysplastic syndromes |
US20040091455A1 (en) * | 2002-10-31 | 2004-05-13 | Zeldis Jerome B. | Methods of using and compositions comprising immunomodulatory compounds for treatment and management of macular degeneration |
US7563810B2 (en) * | 2002-11-06 | 2009-07-21 | Celgene Corporation | Methods of using 3-(4-amino-1-oxo-1,3-dihydroisoindol-2-yl)-piperidine-2,6-dione for the treatment and management of myeloproliferative diseases |
CH696542A5 (de) * | 2003-07-09 | 2007-07-31 | Siegfried Ltd | Verfahren zur Herstellung von substituierten 2,6-Dioxopiperidin-3-yl-Verbindungen. |
ES2430545T3 (es) * | 2005-06-30 | 2013-11-21 | Celgene Corporation | Procedimientos para la preparación de compuestos de 4-amino-2-(2,6-dioxopiperidin-3-il)isoindolina-1,3-diona |
ES2434946T3 (es) * | 2005-08-31 | 2013-12-18 | Celgene Corporation | Compuestos de isoindol imida y composiciones que los comprenden y métodos para usarlo |
JP5567339B2 (ja) * | 2006-09-15 | 2014-08-06 | セルジーン コーポレイション | N−メチルアミノメチルイソインドール化合物、それを含む組成物、及びその使用方法 |
CN101959856A (zh) | 2008-03-11 | 2011-01-26 | 雷迪博士实验室有限公司 | 来那度胺的制备 |
WO2009111948A1 (zh) | 2008-03-13 | 2009-09-17 | 天津和美生物技术有限公司 | 3-(4-氨基-1-氧代-1,3-二氢异吲哚-2-基)哌啶-2,6-二酮及其衍生物的盐或盐的多晶型物及其制备和应用 |
-
2005
- 2005-08-31 EP EP12164781.2A patent/EP2479172B1/en active Active
- 2005-08-31 CA CA2579291A patent/CA2579291C/en active Active
- 2005-08-31 JP JP2007530398A patent/JP2008512379A/ja active Pending
- 2005-08-31 ZA ZA200702382A patent/ZA200702382B/xx unknown
- 2005-08-31 EP EP05793314.5A patent/EP1797068B1/en active Active
- 2005-08-31 ES ES05793314.5T patent/ES2437592T3/es active Active
- 2005-08-31 WO PCT/US2005/031318 patent/WO2006028964A1/en active Application Filing
- 2005-08-31 AU AU2005282728A patent/AU2005282728A1/en not_active Abandoned
- 2005-08-31 BR BRPI0514865-0A patent/BRPI0514865A/pt not_active IP Right Cessation
- 2005-08-31 NZ NZ554068A patent/NZ554068A/en unknown
- 2005-08-31 KR KR1020077007538A patent/KR20070057907A/ko not_active Application Discontinuation
- 2005-08-31 CN CNA2005800372200A patent/CN101080400A/zh active Pending
- 2005-08-31 ES ES12164781.2T patent/ES2438725T3/es active Active
- 2005-08-31 MX MX2007002521A patent/MX2007002521A/es active IP Right Grant
- 2005-09-01 US US11/219,589 patent/US7863451B2/en active Active
- 2005-09-02 AR ARP050103695A patent/AR050724A1/es unknown
- 2005-09-02 GT GT200500242A patent/GT200500242A/es unknown
- 2005-09-02 PE PE2005001015A patent/PE20060648A1/es not_active Application Discontinuation
- 2005-09-02 HN HN2005000508A patent/HN2005000508A/es unknown
- 2005-09-02 TW TW094130010A patent/TW200621748A/zh unknown
- 2005-09-02 PA PA20058643901A patent/PA8643901A1/es unknown
- 2005-09-02 UY UY29097A patent/UY29097A1/es not_active Application Discontinuation
- 2005-09-02 SV SV2005002219A patent/SV2007002219A/es not_active Application Discontinuation
-
2007
- 2007-03-01 IL IL181674A patent/IL181674A0/en unknown
-
2012
- 2012-07-23 JP JP2012162375A patent/JP5701824B2/ja active Active
Also Published As
Publication number | Publication date |
---|---|
WO2006028964A1 (en) | 2006-03-16 |
ZA200702382B (en) | 2008-08-27 |
NZ554068A (en) | 2009-07-31 |
JP2008512379A (ja) | 2008-04-24 |
PE20060648A1 (es) | 2006-07-14 |
TW200621748A (en) | 2006-07-01 |
SV2007002219A (es) | 2007-03-20 |
PA8643901A1 (es) | 2006-05-16 |
AU2005282728A1 (en) | 2006-03-16 |
EP1797068A1 (en) | 2007-06-20 |
CN101080400A (zh) | 2007-11-28 |
JP5701824B2 (ja) | 2015-04-15 |
ES2437592T3 (es) | 2014-01-13 |
EP2479172B1 (en) | 2013-10-09 |
EP1797068B1 (en) | 2013-10-09 |
ES2438725T3 (es) | 2014-01-20 |
AR050724A1 (es) | 2006-11-15 |
IL181674A0 (en) | 2007-07-04 |
US20060052609A1 (en) | 2006-03-09 |
KR20070057907A (ko) | 2007-06-07 |
MX2007002521A (es) | 2007-05-09 |
CA2579291A1 (en) | 2006-03-16 |
UY29097A1 (es) | 2006-03-31 |
EP2479172A1 (en) | 2012-07-25 |
HN2005000508A (es) | 2010-10-08 |
JP2012207040A (ja) | 2012-10-25 |
CA2579291C (en) | 2011-11-29 |
US7863451B2 (en) | 2011-01-04 |
GT200500242A (es) | 2006-06-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BRPI0514865A (pt) | processo para preparar um composto | |
DE60224404D1 (de) | Substiuierte piperidine als melanocortinrezeptor-modulatoren | |
DE60229530D1 (de) | Substituierte piperazine als modulatoren des melanocortinrezeptors | |
NO20063928L (no) | Substituerte kinolinforbindelser | |
NO20062136L (no) | Imidazopyrazintyrosin-kinaseinhibitorer | |
TW200612911A (en) | Compounds for the treatment of inflammatory disorders | |
NO20072747L (no) | Fremgangsmate for fremstilling av indazolforbindelser | |
BRPI0410117A (pt) | composto, composição farmacêutica, método para o tratamento de uma doença ou condição mediada por jak3, e, processo para a preparação de um composto | |
NO20076066L (no) | Oksadiazolderivater som DGAT-inhibitorer | |
MY141867A (en) | Substituted pyrimidines useful as protein kinase inhibitors | |
MX2007011847A (es) | Derivados de pirimidindiona como antagonistas del receptor de procineticina 2. | |
NO20083567L (no) | Hydantoinderivater for behandling av inflammatoriske forstyrrelser | |
MX2022007105A (es) | Formas solidas de sal de 1,3-dihidroxi-2-(hidroximetil)propan-2-am ina de acido 2-((4-((s)-2-(5-cloropiridin-2-il)-2-metilbenzo[d][1, 3] dioxol-4-il)piperidin-1-il)metil)-1-(((s)-oxetan-2-il) metil)-1h- benzo[d]imidazol-6-carboxilico. | |
NO20084318L (no) | Inhibitorer av II-beta-hydroksystereoid dehydrogenase I | |
NO20090166L (no) | Amino-imidazoloner og deres anvendelse som et medikament for behandling av kognitiv svekkelse, Alzheimers sykdom, neurodegenerering og demens | |
TW200720260A (en) | Prokineticin 1 receptor antagonists | |
NO20090755L (no) | Amino-imidazoloner og deres anvendelse som et medikament for behandling av kognitiv svekkelse, Alzheimers sykdom, neurodegenerering og demens | |
EA200900779A1 (ru) | Производные дигидропиридина, полезные как ингибиторы протеинкиназы | |
DE602006013940D1 (de) | Oral zerfallende zusammensetzung von olanzapin oder donepezil | |
WO2007079214A3 (en) | Prokineticin 2 receptor antagonists | |
EA201100311A1 (ru) | Амидные производные гетероарилов и их применение в качестве активаторов глюкокиназы | |
NO20083845L (no) | 2,4-diaminopyrimidiner som celle-cyklus kinase inhibitorer | |
WO2007079163A3 (en) | Prokineticin 1 receptor antagonists | |
ATE432260T1 (de) | Pyridinderivate als pkc-theta-hemmer | |
NO20091463L (no) | Heterocyklisk deriverte metalloproteaseinhibitorer |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
B11A | Dismissal acc. art.33 of ipl - examination not requested within 36 months of filing | ||
B11N | Dismissal: publication cancelled [chapter 11.14 patent gazette] |
Free format text: REFERENTE A RPI NO 2051 DE 27/04/2010. |
|
B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE AS 6A, 7A, 8A, 9A E 10A ANUIDADES. |
|
B08K | Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette] |
Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2342 DE 24-11-2015 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013. |