HRP20020934B1 - 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl in pure crystalline form and process for synthesis - Google Patents

5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl in pure crystalline form and process for synthesis

Info

Publication number
HRP20020934B1
HRP20020934B1 HR20020934A HRP20020934A HRP20020934B1 HR P20020934 B1 HRP20020934 B1 HR P20020934B1 HR 20020934 A HR20020934 A HR 20020934A HR P20020934 A HRP20020934 A HR P20020934A HR P20020934 B1 HRP20020934 B1 HR P20020934B1
Authority
HR
Croatia
Prior art keywords
methanesulfonylphenyl
bipyridinyl
chloro
synthesis
methyl
Prior art date
Application number
HR20020934A
Other languages
English (en)
Croatian (hr)
Inventor
S. Crocker Louis
Ian Davies W.
G. Osifchin Richard
Kotliar Andrew
Original Assignee
Merck Sharp & Dohme Corp.
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22772880&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20020934(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck Sharp & Dohme Corp. filed Critical Merck Sharp & Dohme Corp.
Publication of HRP20020934A2 publication Critical patent/HRP20020934A2/hr
Publication of HRP20020934B1 publication Critical patent/HRP20020934B1/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/61—Halogen atoms or nitro radicals
    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00—Drugs for genital or sexual disorders; Contraceptives
    • A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00—Drugs for dermatological disorders
    • A61P17/02—Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • 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
    • 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
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/06—Antigout agents, e.g. antihyperuricemic or uricosuric agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • 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
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/16—Antivirals for RNA viruses for influenza or rhinoviruses
    • 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)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Biomedical Technology (AREA)
  • Pain & Pain Management (AREA)
  • Neurosurgery (AREA)
  • Virology (AREA)
  • Reproductive Health (AREA)
  • Communicable Diseases (AREA)
  • Rheumatology (AREA)
  • Oncology (AREA)
  • Dermatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Endocrinology (AREA)
  • Immunology (AREA)
  • Molecular Biology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Pregnancy & Childbirth (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
HR20020934A 2000-05-26 2001-05-22 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl in pure crystalline form and process for synthesis HRP20020934B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US20801700P 2000-05-26 2000-05-26
PCT/US2001/016566 WO2001092230A1 (fr) 2000-05-26 2001-05-22 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl- [2,3']bipyridinyl sous forme cristalline pure et procede de synthese

Publications (2)

Publication Number Publication Date
HRP20020934A2 HRP20020934A2 (en) 2005-02-28
HRP20020934B1 true HRP20020934B1 (en) 2012-01-31

Family

ID=22772880

Family Applications (1)

Application Number Title Priority Date Filing Date
HR20020934A HRP20020934B1 (en) 2000-05-26 2001-05-22 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl in pure crystalline form and process for synthesis

Country Status (48)

Country Link
EP (1) EP1296951B1 (fr)
JP (2) JP3665053B2 (fr)
KR (1) KR100757699B1 (fr)
CN (1) CN1227233C (fr)
AR (1) AR028577A1 (fr)
AT (1) ATE483687T1 (fr)
AU (2) AU6480401A (fr)
BG (1) BG65855B1 (fr)
BR (1) BRPI0111140B8 (fr)
CA (1) CA2410234C (fr)
CR (1) CR6606A (fr)
CY (1) CY1111440T1 (fr)
CZ (1) CZ20023888A3 (fr)
DE (1) DE60143197D1 (fr)
DK (1) DK1296951T3 (fr)
EA (1) EA004809B1 (fr)
EE (1) EE05242B1 (fr)
EG (1) EG24189A (fr)
ES (1) ES2351958T3 (fr)
GC (1) GC0000362A (fr)
GE (1) GEP20053492B (fr)
GT (1) GT200100091A (fr)
HN (1) HN2001000110A (fr)
HR (1) HRP20020934B1 (fr)
HU (1) HU228423B1 (fr)
IL (1) IL152582A0 (fr)
IN (2) IN2002CH02089A (fr)
IS (1) IS2806B (fr)
JO (1) JO2216B1 (fr)
MA (1) MA26919A1 (fr)
ME (1) ME00428B (fr)
MX (1) MX230696B (fr)
MY (1) MY123569A (fr)
NO (1) NO324495B1 (fr)
NZ (1) NZ522394A (fr)
PA (1) PA8516901A1 (fr)
PE (1) PE20011324A1 (fr)
PH (1) PH12001001175B1 (fr)
PL (1) PL358153A1 (fr)
PT (1) PT1296951E (fr)
RS (1) RS51541B (fr)
SI (1) SI1296951T1 (fr)
SK (1) SK287174B6 (fr)
SV (1) SV2002000462A (fr)
TW (1) TWI303634B (fr)
UA (1) UA73355C2 (fr)
WO (1) WO2001092230A1 (fr)
ZA (1) ZA200209558B (fr)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6858631B1 (en) 1999-11-29 2005-02-22 Merck & Co., Inc. Polymorphic, amorphous and hydrated forms of 5-chloro-3-(4-methanesulfonylphenyl)-6′-methyl-[2,3′]bipyridinyl
JP4425514B2 (ja) * 1999-11-29 2010-03-03 メルク フロスト カナダ リミテツド ５−クロロ−３−（４−メタンスルホニルフェニル）−６′−メチル−［２，３′］ビピリジニルの多形型、非晶質型および水和型
US6521642B2 (en) * 2000-05-26 2003-02-18 Merck & Co., Inc. 5-chloro-3-(4-methanesulfonylphenyl)-6′-methyl-[2,3′]bipyridinyl in pure crystalline form and process for synthesis
PL2479166T3 (pl) 2009-02-27 2014-11-28 Cadila Healthcare Ltd Sposób otrzymywania etorykoksybu
WO2012004677A1 (fr) 2010-07-05 2012-01-12 Actavis Group Ptc Ehf Formes à l'état solide de sels d'étoricoxib
EA023286B1 (ru) 2011-05-27 2016-05-31 ФАРМА ДжРС, Д.О.О. Способ получения полиморфной формы i эторикоксиба
EP2773618A1 (fr) 2011-11-03 2014-09-10 Cadila Healthcare Limited Procédé amélioré pour la préparation d'étoricoxibe et de polymorphes de celui-ci
WO2013075732A1 (fr) 2011-11-21 2013-05-30 Synthon Bv Procédé de préparation d'une forme cristalline i de l'étoricoxib
EP2601952A1 (fr) 2011-12-07 2013-06-12 Zentiva, k.s. Nouveaux sels et cocrristaux pharmaceutiqement acceptables du 5- chloro-3-(4-méthanesulfonylphényl)-6'-méthyl-[2,3'] bipyridinyle et leurs utilisations thérapeutiques
ES2630051T3 (es) 2012-08-27 2017-08-17 Cadila Healthcare Limited Composición farmacéutica de etoricoxib
EP2888231B1 (fr) 2012-08-27 2019-01-09 Glenmark Pharmaceuticals Limited Procédé de préparation d'étoricoxib cristallin
CN104418799A (zh) * 2013-09-03 2015-03-18 天津药物研究院 一种依托考昔的晶型及其制备方法和应用
WO2015036550A1 (fr) 2013-09-13 2015-03-19 Synthon B.V. Procédé pour la préparation d'étoricoxib
CN106632003B (zh) * 2015-12-31 2019-02-12 上海博志研新药物技术有限公司 一种依托考昔的制备方法
CN108069896B (zh) * 2016-11-11 2022-08-12 昆明积大制药股份有限公司 一种依托考昔晶型的制备方法
CN107417599B (zh) * 2017-06-21 2020-06-09 四川尚锐生物医药有限公司 一种依托考昔晶型的制备方法
CN107056691B (zh) * 2017-06-21 2020-03-10 四川尚锐生物医药有限公司 一种制备依托考昔晶型v的方法
MX2017009660A (es) 2017-07-26 2017-11-23 Laboratorios Liomont S A De C V Composicion farmaceutica con un rango de relacion entre el clorhidrato de tramadol y el etoricoxib para su administracion para el tratamiento del dolor.
CN107556231A (zh) * 2017-09-23 2018-01-09 江苏正大清江制药有限公司 一种依托考昔与对硝基苯甲酸形成的盐的晶型及制备方法
CN107417600A (zh) * 2017-09-26 2017-12-01 江苏正大清江制药有限公司 一种依托考昔与呋喃甲酸形成盐的新晶型及制备方法
CN107898787B (zh) * 2017-12-15 2018-11-30 扬子江药业集团上海海尼药业有限公司 一种药物组合物及其制剂和制备方法
WO2019130049A1 (fr) 2017-12-29 2019-07-04 Grünenthal GmbH Combinaison pharmaceutique comprenant du chlorhydrate de tramadol à libération prolongée et de l'étoricoxib à libération immédiate, et son utilisation pour le traitement de la douleur
CN110143915A (zh) * 2019-06-03 2019-08-20 蚌埠学院 一种依托考昔与对甲苯磺酸形成盐的新晶型及制备方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998003484A1 (fr) * 1996-07-18 1998-01-29 Merck Frosst Canada Inc. Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2
WO1999055830A2 (fr) * 1998-04-24 1999-11-04 Merck & Co., Inc. Procede de synthese d'inhibiteurs de cox-2
WO2001037833A1 (fr) * 1999-11-29 2001-05-31 Merck Frosst Canada & Co. Formes polymorphes, amorphes et hydratees de 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyle

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5593994A (en) * 1994-09-29 1997-01-14 The Dupont Merck Pharmaceutical Company Prostaglandin synthase inhibitors
US5739166A (en) * 1994-11-29 1998-04-14 G.D. Searle & Co. Substituted terphenyl compounds for the treatment of inflammation
US5861419A (en) * 1996-07-18 1999-01-19 Merck Frosst Canad, Inc. Substituted pyridines as selective cyclooxygenase-2 inhibitors

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998003484A1 (fr) * 1996-07-18 1998-01-29 Merck Frosst Canada Inc. Pyridines substituees en tant qu'inhibiteurs selectifs de la cyclo-oxygenase-2
WO1999055830A2 (fr) * 1998-04-24 1999-11-04 Merck & Co., Inc. Procede de synthese d'inhibiteurs de cox-2
WO2001037833A1 (fr) * 1999-11-29 2001-05-31 Merck Frosst Canada & Co. Formes polymorphes, amorphes et hydratees de 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyle

Also Published As

Publication number Publication date
GEP20053492B (en) 2005-04-25
AU6480401A (en) 2001-12-11
BG65855B1 (bg) 2010-03-31
EE200200655A (et) 2004-08-16
KR20030003762A (ko) 2003-01-10
HRP20020934A2 (en) 2005-02-28
CR6606A (es) 2006-02-06
JP4142621B2 (ja) 2008-09-03
MA26919A1 (fr) 2004-12-20
NO324495B1 (no) 2007-10-29
YU89402A (sh) 2005-11-28
IL152582A0 (en) 2003-05-29
AR028577A1 (es) 2003-05-14
HU228423B1 (en) 2013-03-28
CY1111440T1 (el) 2015-08-05
DE60143197D1 (de) 2010-11-18
JP2005047927A (ja) 2005-02-24
SV2002000462A (es) 2002-03-08
PA8516901A1 (es) 2002-04-25
IN2007CH05103A (fr) 2008-08-27
EA200201264A1 (ru) 2003-04-24
UA73355C2 (en) 2005-07-15
NO20025674L (no) 2002-11-26
JP3665053B2 (ja) 2005-06-29
BG107237A (bg) 2003-05-30
EA004809B1 (ru) 2004-08-26
MXPA02011619A (es) 2003-03-27
PT1296951E (pt) 2010-12-07
HK1058932A1 (en) 2004-06-11
EE05242B1 (et) 2009-12-15
MY123569A (en) 2006-05-31
PE20011324A1 (es) 2002-01-28
CA2410234A1 (fr) 2001-12-06
EP1296951A1 (fr) 2003-04-02
NO20025674D0 (no) 2002-11-26
HN2001000110A (es) 2002-03-06
BR0111140A (pt) 2005-01-11
SK16702002A3 (sk) 2003-05-02
ZA200209558B (en) 2003-10-28
IN2002CH02089A (fr) 2005-02-25
ATE483687T1 (de) 2010-10-15
ME00428B (me) 2011-10-10
AU2001264804B2 (en) 2006-04-06
BRPI0111140B1 (pt) 2018-03-13
IS6630A (is) 2002-11-20
JO2216B1 (en) 2004-10-07
MX230696B (es) 2005-09-19
IS2806B (is) 2012-09-15
HUP0302336A2 (hu) 2003-11-28
GT200100091A (es) 2001-12-28
CZ20023888A3 (cs) 2003-02-12
WO2001092230A1 (fr) 2001-12-06
PH12001001175B1 (en) 2006-08-10
RS51541B (sr) 2011-06-30
CA2410234C (fr) 2008-05-13
BRPI0111140B8 (pt) 2021-05-25
TWI303634B (en) 2008-12-01
EG24189A (en) 2008-10-08
PL358153A1 (en) 2004-08-09
SI1296951T1 (sl) 2011-01-31
KR100757699B1 (ko) 2007-09-13
GC0000362A (en) 2007-03-31
CN1227233C (zh) 2005-11-16
CN1443168A (zh) 2003-09-17
NZ522394A (en) 2004-05-28
EP1296951B1 (fr) 2010-10-06
SK287174B6 (sk) 2010-02-08
DK1296951T3 (da) 2011-01-24
ES2351958T3 (es) 2011-02-14
JP2004501116A (ja) 2004-01-15

Similar Documents

Publication Publication Date Title
HRP20020934B1 (en) 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl in pure crystalline form and process for synthesis
HRP20000168B1 (en) Resorcinol derivatives
MXPA02012905A (es) Derivados de colquinol como agentes de dano vascular..
MY142768A (en) Gfat inhibitors
MXPA02012034A (es) Derivados de tiofeno utiles como agentes anticancerosos.
WO2002080846A3 (fr) Derives d'epothilone : procedes de fabrication et methodes d'utilisation associes
IL181298A0 (en) Solid and crystalline ibandronate sodium and processes for preparation thereof
ZA992017B (en) Chemical compounds.
HRP20000171B1 (en) Oral compositions of levosimendan
MXPA02003977A (es) Inhibidores de adhesion de celula mediada por al°2.
BG107532A (en) Novel alpha chrystalline form of perindopril tert-butylamine salts, preparation method and pharmaceutical compositions containing same
YU100502A (sh) Novi $g (b) kristalni oblik tercijalne butilaminske soli perindoprila, postupak dobijanja i farmaceutske kompozicije koje sadrže isto
ES2132415T3 (es) Nuevos derivados de 5-pirrolil-2-piridilmetilsulfinilbencimidazol.
BR0206372A (pt) Processo para sintetizar um composto
MXPA02009643A (es) Sintesis acortada de derivados de 3,3-diarilpropilamina.
CA2508824A1 (fr) Forme cristalline alpha du ranelate de strontium, son procede de preparation, et les compositions pharmaceutiques qui la contiennent
MEP15708A (en) Lithium complexes of n-(1-hydroxymethyl-2,3-dihydroxypropyl)-1,4,7-triscarboxymethyl-1,4,7,10-tetraazacyclododecane, production and use thereof
GEP20043365B (en) Polymorphic Salt
AU2174483A (en) New vitro alphatic compounds
DE60206068D1 (de) Aralkyltetrahydropyridine, deren herstellung und pharmazeutische zusammensetzungen, die diese enthalten
TW200502235A (en) Novel benzo[1,2,5]thiadiazoles and pharmaceutical use thereof
WO2001080906A3 (fr) Complexes radiometalliques de 2-pyrrolylthiones et leur utilisation comme agents radiopharmaceutiques d'imagerie et de therapie
AU5125798A (en) Novel n-benzenesulphonyl-l-proline derivatives, method for preparing and therapeutic use
ATE355281T1 (de) 1,4,7,10-tetraazacyclododecan-1,4-diessigsäure
WO2004065360A3 (fr) Nouveaux derives de piperazine et leur utilisation comme intermediaires de synthese

Legal Events

Date Code Title Description
A1OB Publication of a patent application
ARAI Request for the grant of a patent on the basis of the submitted results of a substantive examination of a patent application
PNAN Change of the applicant name, address/residence

Owner name: MERCK SHARP & DOHME CORP., US

B1PR Patent granted
PNAN Change of the applicant name, address/residence

Owner name: SCHERING CORPORATION, US

Owner name: MERCK SHARP & DOHME CORP., US

ODRP Renewal fee for the maintenance of a patent

Payment date: 20190507

Year of fee payment: 19

ODRP Renewal fee for the maintenance of a patent

Payment date: 20200505

Year of fee payment: 20

PB20 Patent expired after termination of 20 years

Effective date: 20210522