UA81365C2 - Ccr-2 antagonist salt, method for modulation of chemokine receptor activity, method for treating (variants) and pharmaceutical composition - Google Patents

Ccr-2 antagonist salt, method for modulation of chemokine receptor activity, method for treating (variants) and pharmaceutical composition Download PDF

Info

Publication number
UA81365C2
UA81365C2 UAA200605772A UAA200605772A UA81365C2 UA 81365 C2 UA81365 C2 UA 81365C2 UA A200605772 A UAA200605772 A UA A200605772A UA A200605772 A UAA200605772 A UA A200605772A UA 81365 C2 UA81365 C2 UA 81365C2
Authority
UA
Ukraine
Prior art keywords
solution
added
naphthyridine
trifluoromethyl
pyran
Prior art date
Application number
UAA200605772A
Other languages
English (en)
Ukrainian (uk)
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of UA81365C2 publication Critical patent/UA81365C2/uk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs 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)
UAA200605772A 2003-10-27 2004-10-25 Ccr-2 antagonist salt, method for modulation of chemokine receptor activity, method for treating (variants) and pharmaceutical composition UA81365C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US51473503P 2003-10-27 2003-10-27
PCT/US2004/035069 WO2005044264A1 (fr) 2003-10-27 2004-10-25 Sel antagoniste de ccr-2

Publications (1)

Publication Number Publication Date
UA81365C2 true UA81365C2 (en) 2007-12-25

Family

ID=34572774

Family Applications (1)

Application Number Title Priority Date Filing Date
UAA200605772A UA81365C2 (en) 2003-10-27 2004-10-25 Ccr-2 antagonist salt, method for modulation of chemokine receptor activity, method for treating (variants) and pharmaceutical composition

Country Status (21)

Country Link
US (1) US7473696B2 (fr)
EP (1) EP1682135B1 (fr)
JP (1) JP4542550B2 (fr)
KR (1) KR20060101476A (fr)
CN (1) CN1870998B (fr)
AT (1) ATE517622T1 (fr)
AU (1) AU2004287416C1 (fr)
BR (1) BRPI0415836A (fr)
CA (1) CA2543201C (fr)
CO (1) CO5690606A2 (fr)
EC (1) ECSP066524A (fr)
IL (1) IL175009A0 (fr)
IS (1) IS8400A (fr)
MA (1) MA28104A1 (fr)
MX (1) MXPA06004647A (fr)
NO (1) NO20062377L (fr)
NZ (1) NZ546447A (fr)
RU (1) RU2317295C1 (fr)
UA (1) UA81365C2 (fr)
WO (1) WO2005044264A1 (fr)
ZA (1) ZA200602752B (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
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 (fr) 2002-11-27 2012-04-25 Incyte Corporation Derives de la 3-aminopyrrolidine modulateurs des recepteurs de la chemoquine
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 (fr) 2004-06-28 2006-01-12 Incyte Corporation 3-aminocyclopentanecarboxamides utilises en tant que modulateurs des recepteurs des chimiokines
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 (fr) * 2011-03-17 2012-09-20 Merck Sharp & Dohme Corp. Dérivés d'amino cyclopentane substitués par cyclohexane en tant qu'antagonistes utiles de ccr2
WO2013149376A1 (fr) 2012-04-02 2013-10-10 Abbott Laboratories Antagonistes de récepteurs de chimiokines
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)

* Cited by examiner, † Cited by third party
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 (fr) * 1999-06-11 2000-12-21 Merck & Co., Inc. Modulateurs cyclopentyliques de l'activite du recepteur de la chimiokine
EP1318811B1 (fr) 2000-08-17 2006-08-30 Merck & Co., Inc. Modulateurs cyclopentyles de l'activite du recepteur de la chimiokine
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 (fr) * 2001-11-29 2006-03-15 Pfizer Products Inc. Sels succiniques de 5,8,14-triazatetracyclo 10.3.1.02,11.0 4,9 -hexadeca-2(11),3,5,7,9-pentaene et compositions pharmaceutiques associees
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 (fr) * 2002-04-29 2008-05-28 Merck & Co., Inc. Modulateurs tetrahydropyranyl cyclopentyl tetrahydropyridopyridine de l'activite des recepteurs de chimiokine
AR045875A1 (es) * 2003-10-27 2005-11-16 Merck & Co Inc Procedimiento para la preparacion del antagonista ccr-2

Also Published As

Publication number Publication date
AU2004287416C1 (en) 2010-09-09
EP1682135A1 (fr) 2006-07-26
RU2317295C1 (ru) 2008-02-20
EP1682135B1 (fr) 2011-07-27
KR20060101476A (ko) 2006-09-25
ATE517622T1 (de) 2011-08-15
BRPI0415836A (pt) 2007-01-02
IS8400A (is) 2006-04-06
JP2007509940A (ja) 2007-04-19
AU2004287416B2 (en) 2009-11-19
ZA200602752B (en) 2007-08-29
EP1682135A4 (fr) 2009-11-25
JP4542550B2 (ja) 2010-09-15
CN1870998B (zh) 2010-10-20
NO20062377L (no) 2006-05-24
CA2543201C (fr) 2010-12-21
CO5690606A2 (es) 2006-10-31
MXPA06004647A (es) 2006-06-27
WO2005044264A1 (fr) 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 (fr) 2005-05-19
CN1870998A (zh) 2006-11-29

Similar Documents

Publication Publication Date Title
UA81365C2 (en) Ccr-2 antagonist salt, method for modulation of chemokine receptor activity, method for treating (variants) and pharmaceutical composition
ES2550485T3 (es) Intermedios de inhibidores de la endopeptidasa neutra y método de preparación de los mismos
ES2266671T3 (es) Proceso para la produccion de estatinas semisinteticas a traves de nuevos intermediarios.
Breuning et al. An improved synthesis of aziridine-2, 3-dicarboxylates via azido alcohols—epimerization studies
KR20200008578A (ko) (3R,4S)-3-아세트아미도-4-알릴-N-(tert-부틸)피롤리딘-3-카복스아미드의 제조방법
RU2126379C1 (ru) ПРОИЗВОДНЫЕ ЦИКЛОПЕНТАН- ИЛИ ЦИКЛОПЕНТЕН -β- АМИНОКИСЛОТ И ИХ СОЛИ, КОМПОЗИЦИЯ, АКТИВНАЯ В ОТНОШЕНИИ ШТАММОВ S.AUREUS CANDIDA И TRICHOPHYTON
AU2024251729A1 (en) Synthesis of ras inhibitors
JP6596417B2 (ja) インドール化合物の製造方法
AU2004287810B2 (en) Process for the preparation of CCR-2 antagonist
CN107250100A (zh) 制备nep抑制剂的工艺和中间体
ES2392207T3 (es) Proceso a partir de ácido shikímico para obtener oseltamivir fosfato
US7528264B2 (en) Hydride reduction process for preparing quinolone intermediates
AU2003299042A1 (en) Process for the synthesis of intermediates useful for the synthesis of tubulin inhibitors
KR20110104933A (ko) 피페리딘 유도체의 입체선택적 합성
RU2628081C2 (ru) Способы и промежуточные соединения для получения макроциклических ингибиторов протеазы hcv
JP2014240399A (ja) イソキノリン誘導体又はその塩の新規製造方法
WO2006095362A1 (fr) Procede de preparation du levetiracetam
KR20180115743A (ko) 신규 독소, 및 이의 중간체를 제조하는 방법
BG63392B1 (bg) Производни на 5-нафтален-1-ил-1,3-диоксан, тяхното получаване и използването им като терапевтични средства
CN101486668A (zh) 酰氧基烃基氨基甲酸酯前药及其中间体的合成
ES2383861B1 (es) Procedimiento de síntesis de intermedios de crambescidinas, de cimipronidina y de sus derivados.
JPWO2004058710A1 (ja) 新規ベンズアミド誘導体及びその製造法
MXPA01002058A (en) Tan-1057 derivatives