BRPI0415836A - composto, métodos para a modulação da atividade de receptor de quimocina em um mamìfero, e para o tratamento, a melhoria, o controle ou a redução do risco de uma doença ou distúrbio inflamatório e imunorregulatório, e de artrite reumatóide, composição farmacêutica - Google Patents
composto, métodos para a modulação da atividade de receptor de quimocina em um mamìfero, e para o tratamento, a melhoria, o controle ou a redução do risco de uma doença ou distúrbio inflamatório e imunorregulatório, e de artrite reumatóide, composição farmacêuticaInfo
- Publication number
- BRPI0415836A BRPI0415836A BRPI0415836-9A BRPI0415836A BRPI0415836A BR PI0415836 A BRPI0415836 A BR PI0415836A BR PI0415836 A BRPI0415836 A BR PI0415836A BR PI0415836 A BRPI0415836 A BR PI0415836A
- Authority
- BR
- Brazil
- Prior art keywords
- ameliorating
- mammal
- disorder
- inflammatory
- risk
- Prior art date
Links
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title 2
- 102000009410 Chemokine receptor Human genes 0.000 title 1
- 108050000299 Chemokine receptor Proteins 0.000 title 1
- 241000124008 Mammalia Species 0.000 title 1
- 150000001875 compounds Chemical class 0.000 title 1
- 201000010099 disease Diseases 0.000 title 1
- 208000035475 disorder Diseases 0.000 title 1
- 230000000694 effects Effects 0.000 title 1
- 230000004957 immunoregulator effect Effects 0.000 title 1
- 230000002757 inflammatory effect Effects 0.000 title 1
- 239000008194 pharmaceutical composition Substances 0.000 title 1
- 206010039073 rheumatoid arthritis Diseases 0.000 title 1
- 150000003890 succinate salts Chemical class 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic 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
- C07D471/02—Heterocyclic 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
- C07D471/04—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
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
"COMPOSTO, MéTODOS PARA A MODULAçãO DA ATIVIDADE DE RECEPTOR DE QUIMOCINA EM UM MAMìFERO, E PARA O TRATAMENTO, A MELHORIA, O CONTROLE OU A REDUçãO DO RISCO DE UMA DOENçA OU DISTúRBIO INFLAMATóRIO E IMUNORREGULATóRIO, E DE ARTRITE REUMATóIDE, COMPOSIçãO FARMACêUTICA". A presente invenção proporciona uma sintese eficiente para a preparação de ((1R,3S)-3-isopropil-3-{¢3-(trifluorometil)-7,8-di-hidro-1,6-naftiridin-6(5 H)-il!-carbonil}-ciclo-pentil)¢(3S,4S)-3-metóxi-tetra-hidro-2H-piran-4-il!- amina e seu sal de succinato. A presente invenção adicionalmente proporciona uma síntese eficiente para a preparação de intermediários (3R)-3-metóxi-tetra-hidro-4H-piran-4-ona; ácido (1S,4S)-4-(2,5-dimetil-1H-pirrol-1-il)-1-isopropil-ciclo-pent-2-eno-1-car boxílico; e 3-(trifluorometil)-5,6,7,8-tetra-hidro- 1,6-naftiridina; e para a preparação do precursor (3S,4S)-N-((1S,4S)-4-isopropil-4-{¢3-trifluorometil)-7,8-di-hidro-1,6-naft iridin-6(5H)il!-carbonil}-ciclo-pent-2-en-1-il)-3-metóxi-tetra-hidro-2H-pir an-4-amina. A invenção adicionalmente reside nas propriedades superiores do sal de succinato de ((1R,3S)-3-isopropil-3-{¢3-(trifluorometil)-7,8-di-hidro-1,6-naftiridin-6(5 H)-il!-carbonil}-ciclo-pentil)¢(3S,4S)-3-metóxi-tetra-hidro-2H-piran-4-il!- amina.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51473503P | 2003-10-27 | 2003-10-27 | |
| PCT/US2004/035069 WO2005044264A1 (en) | 2003-10-27 | 2004-10-25 | Ccr-2 antagonist salt |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| BRPI0415836A true BRPI0415836A (pt) | 2007-01-02 |
Family
ID=34572774
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BRPI0415836-9A BRPI0415836A (pt) | 2003-10-27 | 2004-10-25 | composto, métodos para a modulação da atividade de receptor de quimocina em um mamìfero, e para o tratamento, a melhoria, o controle ou a redução do risco de uma doença ou distúrbio inflamatório e imunorregulatório, e de artrite reumatóide, composição farmacêutica |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US7473696B2 (pt) |
| EP (1) | EP1682135B1 (pt) |
| JP (1) | JP4542550B2 (pt) |
| KR (1) | KR20060101476A (pt) |
| CN (1) | CN1870998B (pt) |
| AT (1) | ATE517622T1 (pt) |
| AU (1) | AU2004287416C1 (pt) |
| BR (1) | BRPI0415836A (pt) |
| CA (1) | CA2543201C (pt) |
| CO (1) | CO5690606A2 (pt) |
| EC (1) | ECSP066524A (pt) |
| IL (1) | IL175009A0 (pt) |
| IS (1) | IS8400A (pt) |
| MA (1) | MA28104A1 (pt) |
| MX (1) | MXPA06004647A (pt) |
| NO (1) | NO20062377L (pt) |
| NZ (1) | NZ546447A (pt) |
| RU (1) | RU2317295C1 (pt) |
| UA (1) | UA81365C2 (pt) |
| WO (1) | WO2005044264A1 (pt) |
| ZA (1) | ZA200602752B (pt) |
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20060030582A1 (en) * | 2002-04-29 | 2006-02-09 | Demartino Julie | Tetrahydropyranyl cyclopentyl tetrahydropyridopyridine modulators of chemokine receptor activity |
| JO2479B1 (en) | 2002-04-29 | 2009-01-20 | ميرك شارب اند دوم ليمتد | Rates for the activity of the chemokine receptor of tetrahydrobranyl cycloneptil tetrahydrobredo predine |
| EP1565436B1 (en) | 2002-11-27 | 2012-04-25 | Incyte Corporation | 3-aminopyrrolidine derivatives as modulators of chemokine receptors |
| CN1826334A (zh) * | 2003-03-18 | 2006-08-30 | 麦克公司 | 趋化因子受体活性的四氢吡喃基环戊基杂环酰胺调节剂 |
| AR045875A1 (es) * | 2003-10-27 | 2005-11-16 | Merck & Co Inc | Procedimiento para la preparacion del antagonista ccr-2 |
| KR20080052683A (ko) | 2003-12-18 | 2008-06-11 | 인사이트 코포레이션 | 케모킨 수용체의 조절제로서의3-사이클로알킬아미노피롤리딘 유도체 |
| BRPI0510665A (pt) | 2004-05-11 | 2007-12-04 | Incyte Corp | 3-(4-heteroarilcicloexilamino) ciclopentano-carboxiamidas como moduladores de receptores de quimiocinas |
| GB0413605D0 (en) * | 2004-06-17 | 2004-07-21 | Addex Pharmaceuticals Sa | Novel compounds |
| MXPA06014672A (es) | 2004-06-28 | 2007-03-26 | Incyte Corp | 3-aminociclopentanocarboxamidas como moduladores de receptores de quimioquinas. |
| WO2006004741A2 (en) | 2004-06-28 | 2006-01-12 | Incyte Corporation | 3-aminocyclopentanecarboxamides as modulators of chemokine receptors |
| CN101534824A (zh) | 2006-11-17 | 2009-09-16 | 艾博特公司 | 作为化学活素受体拮抗剂的氨基吡咯烷 |
| US20090076065A1 (en) * | 2007-09-17 | 2009-03-19 | Protia, Llc | Deuterium-enriched mk-0812 |
| US7741327B2 (en) | 2008-04-16 | 2010-06-22 | Hoffmann-La Roche Inc. | Pyrrolidinone glucokinase activators |
| US8178689B2 (en) | 2010-06-17 | 2012-05-15 | Hoffman-La Roche Inc. | Tricyclic compounds |
| WO2012125663A2 (en) * | 2011-03-17 | 2012-09-20 | Merck Sharp & Dohme Corp. | Cyclohexane substituted amino cyclopentane derivatives as useful ccr2 antagonists |
| WO2013149376A1 (en) | 2012-04-02 | 2013-10-10 | Abbott Laboratories | Chemokine receptor antagonists |
| HK1216233A1 (zh) | 2013-02-28 | 2016-10-28 | 参天制药株式会社 | 含有四氢吡喃基氨基环戊基羰基四氢吡啶并吡啶衍生物作为有效成分的眼後段疾病的预防或治疗剂 |
| DK3297438T3 (da) | 2015-05-21 | 2022-01-17 | Chemocentryx Inc | Ccr2-modulatorer |
| CA3293051A1 (en) | 2017-09-25 | 2026-03-02 | Chemocentryx, Inc. | Combination therapy using a chemokine receptor 2 (ccr2) antagonist and a pd-1/pd-l1 inhibitor |
| CN112105353B (zh) | 2018-01-08 | 2024-04-19 | 凯莫森特里克斯股份有限公司 | Ccr2拮抗剂治疗实体瘤的方法 |
| US20190269664A1 (en) | 2018-01-08 | 2019-09-05 | Chemocentryx, Inc. | Methods of treating solid tumors with ccr2 antagonists |
| CN112341350A (zh) * | 2020-10-19 | 2021-02-09 | 江苏威奇达药业有限公司 | 酶法拆分γ-内酰胺后副产物的处理方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RO108347B1 (ro) * | 1989-10-30 | 1994-04-28 | Bellon Labor Sa Roger | DERIVATI DE BENZO-(b)-NAFTIRIDIN-1,8 SI PROCEDEU DE PREPARARE A ACESTORA |
| GB9417249D0 (en) * | 1994-08-26 | 1994-10-19 | Wellcome Found | A novel salt |
| JPH09291034A (ja) * | 1996-02-27 | 1997-11-11 | Yoshitomi Pharmaceut Ind Ltd | 縮合ピリジン化合物およびその医薬としての用途 |
| RU2174123C2 (ru) * | 1996-10-28 | 2001-09-27 | Новартис Аг | Производные 8-арил-1,7-нафтиридина и фармацевтическая композиция, обладающая противовоспалительной активностью |
| US6312689B1 (en) * | 1998-07-23 | 2001-11-06 | Millennium Pharmaceuticals, Inc. | Anti-CCR2 antibodies and methods of use therefor |
| FR2787790A1 (fr) * | 1998-12-23 | 2000-06-30 | Sanofi Sa | Procede de preparation du (r)-(+)-3-{1[2-(4-benzoyl-2-(3,4- difluorophenyl)morpholin-2-yl)ethyl]-4-phenylpiperidin-4-yl} -1,1-dimethyluree, de ses sels, solvats et/ou hydrates |
| WO2000076512A1 (en) * | 1999-06-11 | 2000-12-21 | Merck & Co., Inc. | Cyclopentyl modulators of chemokine receptor activity |
| EP1318811B1 (en) | 2000-08-17 | 2006-08-30 | Merck & Co., Inc. | Cyclopentyl modulators of chemokine receptor activity |
| IL155371A0 (en) * | 2000-11-28 | 2003-11-23 | Pfizer Prod Inc | Salts of a isothiazole-4-carboxamide and their use as anti-hyperproliferation agents |
| EP1461040B1 (en) * | 2001-11-29 | 2006-03-15 | Pfizer Products Inc. | Succinic acid salts of 5,8,14-triazatetracyclo[10.3.1.0 2,11 .0 4,9 ]-hexadeca-2(11),3,5,7,9,-pentaene and pharmaceutical compositions thereof |
| PL370858A1 (en) * | 2001-12-12 | 2005-05-30 | Pfizer Products Inc. | Salt forms of e-2-methoxy-n-(3-{4-[3-methyl-4-(6-methyl-pyridin-3-yloxy)-phenylamino]-quinazolin-6-yl}-allyl)-acetamide and method of production |
| DE60322877D1 (de) * | 2002-04-29 | 2008-09-25 | Merck Sharp & Dohme | Tetrahydropyranylcyclopentyltetrahydroisochino-linmodulatoren der chemokinrezeptoraktivität |
| JO2479B1 (en) | 2002-04-29 | 2009-01-20 | ميرك شارب اند دوم ليمتد | Rates for the activity of the chemokine receptor of tetrahydrobranyl cycloneptil tetrahydrobredo predine |
| EP1501507B1 (en) * | 2002-04-29 | 2008-05-28 | Merck & Co., Inc. | Tetrahydropyranyl cyclopentyl tetrahydropyridopyridine modulators of chemokine receptor activity |
| AR045875A1 (es) * | 2003-10-27 | 2005-11-16 | Merck & Co Inc | Procedimiento para la preparacion del antagonista ccr-2 |
-
2004
- 2004-10-25 MX MXPA06004647A patent/MXPA06004647A/es active IP Right Grant
- 2004-10-25 RU RU2006118352/04A patent/RU2317295C1/ru not_active IP Right Cessation
- 2004-10-25 CA CA2543201A patent/CA2543201C/en not_active Expired - Fee Related
- 2004-10-25 NZ NZ546447A patent/NZ546447A/en unknown
- 2004-10-25 US US10/577,584 patent/US7473696B2/en not_active Expired - Fee Related
- 2004-10-25 WO PCT/US2004/035069 patent/WO2005044264A1/en not_active Ceased
- 2004-10-25 BR BRPI0415836-9A patent/BRPI0415836A/pt not_active IP Right Cessation
- 2004-10-25 UA UAA200605772A patent/UA81365C2/uk unknown
- 2004-10-25 JP JP2006538125A patent/JP4542550B2/ja not_active Expired - Fee Related
- 2004-10-25 EP EP04796120A patent/EP1682135B1/en not_active Expired - Lifetime
- 2004-10-25 AT AT04796120T patent/ATE517622T1/de not_active IP Right Cessation
- 2004-10-25 AU AU2004287416A patent/AU2004287416C1/en not_active Ceased
- 2004-10-25 CN CN2004800315947A patent/CN1870998B/zh not_active Expired - Fee Related
- 2004-10-25 KR KR1020067008066A patent/KR20060101476A/ko not_active Ceased
-
2006
- 2006-04-04 ZA ZA200602752A patent/ZA200602752B/xx unknown
- 2006-04-06 IS IS8400A patent/IS8400A/is unknown
- 2006-04-20 IL IL175009A patent/IL175009A0/en unknown
- 2006-04-24 MA MA28957A patent/MA28104A1/fr unknown
- 2006-04-25 CO CO06039063A patent/CO5690606A2/es unknown
- 2006-04-26 EC EC2006006524A patent/ECSP066524A/es unknown
- 2006-05-24 NO NO20062377A patent/NO20062377L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004287416C1 (en) | 2010-09-09 |
| EP1682135A1 (en) | 2006-07-26 |
| RU2317295C1 (ru) | 2008-02-20 |
| EP1682135B1 (en) | 2011-07-27 |
| KR20060101476A (ko) | 2006-09-25 |
| ATE517622T1 (de) | 2011-08-15 |
| UA81365C2 (en) | 2007-12-25 |
| IS8400A (is) | 2006-04-06 |
| JP2007509940A (ja) | 2007-04-19 |
| AU2004287416B2 (en) | 2009-11-19 |
| ZA200602752B (en) | 2007-08-29 |
| EP1682135A4 (en) | 2009-11-25 |
| JP4542550B2 (ja) | 2010-09-15 |
| CN1870998B (zh) | 2010-10-20 |
| NO20062377L (no) | 2006-05-24 |
| CA2543201C (en) | 2010-12-21 |
| CO5690606A2 (es) | 2006-10-31 |
| MXPA06004647A (es) | 2006-06-27 |
| WO2005044264A1 (en) | 2005-05-19 |
| NZ546447A (en) | 2009-02-28 |
| IL175009A0 (en) | 2006-08-20 |
| US7473696B2 (en) | 2009-01-06 |
| ECSP066524A (es) | 2006-10-10 |
| US20070135474A1 (en) | 2007-06-14 |
| AU2004287416A1 (en) | 2005-05-19 |
| MA28104A1 (fr) | 2006-08-01 |
| CA2543201A1 (en) | 2005-05-19 |
| CN1870998A (zh) | 2006-11-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| B06F | Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette] | ||
| B25D | Requested change of name of applicant approved |
Owner name: MERCK SHARP AND DOHME CORP. (US) Free format text: ALTERADO DE: MERCK AND CO., INC. |
|
| B15K | Others concerning applications: alteration of classification |
Free format text: PARA: INT. CL. A61K 31/4375; C07D 471/04; A61P 19/02 Ipc: A61K 31/4375 (2011.01), C07D 471/04 (2011.01), A61 |
|
| B08F | Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette] |
Free format text: REFERENTE A 7A ANUIDADE. |
|
| 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: REFERENTE AO DESPACHO 8.6 PUBLICADO NA RPI 2158 DE 15/05/2012. |