ES2259295T3 - Formas polimorficas, amorfas e hidratadas de 5-cloro-3-(4-metanosulfonilfenil)-6'-metil-(2,3')bipiridinilo. - Google Patents

Formas polimorficas, amorfas e hidratadas de 5-cloro-3-(4-metanosulfonilfenil)-6'-metil-(2,3')bipiridinilo.

Info

Publication number
ES2259295T3
ES2259295T3 ES00980817T ES00980817T ES2259295T3 ES 2259295 T3 ES2259295 T3 ES 2259295T3 ES 00980817 T ES00980817 T ES 00980817T ES 00980817 T ES00980817 T ES 00980817T ES 2259295 T3 ES2259295 T3 ES 2259295T3
Authority
ES
Spain
Prior art keywords
compound
polymorph
formula
temperature
approximately
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES00980817T
Other languages
English (en)
Spanish (es)
Inventor
Sophie Dorothee Clas
Paul O'shea
Chad Dalton
Louis S. Crocker
James A. Mccauley
Richard D. Tillyer
Ian Davies
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck Frosst Canada and Co
Merck and Co Inc
Original Assignee
Merck Frosst Canada and Co
Merck and 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 Frosst Canada and Co, Merck and Co Inc filed Critical Merck Frosst Canada and Co
Application granted granted Critical
Publication of ES2259295T3 publication Critical patent/ES2259295T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/61Halogen atoms or nitro radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
ES00980817T 1999-11-29 2000-11-27 Formas polimorficas, amorfas e hidratadas de 5-cloro-3-(4-metanosulfonilfenil)-6'-metil-(2,3')bipiridinilo. Expired - Lifetime ES2259295T3 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16792299P 1999-11-29 1999-11-29
US167922P 1999-11-29

Publications (1)

Publication Number Publication Date
ES2259295T3 true ES2259295T3 (es) 2006-10-01

Family

ID=22609368

Family Applications (1)

Application Number Title Priority Date Filing Date
ES00980817T Expired - Lifetime ES2259295T3 (es) 1999-11-29 2000-11-27 Formas polimorficas, amorfas e hidratadas de 5-cloro-3-(4-metanosulfonilfenil)-6'-metil-(2,3')bipiridinilo.

Country Status (11)

Country Link
US (3) US6441002B1 (https=)
EP (1) EP1248618B1 (https=)
JP (1) JP4425514B2 (https=)
AT (1) ATE320809T1 (https=)
AU (1) AU776544B2 (https=)
CA (1) CA2391650C (https=)
DE (1) DE60026877T2 (https=)
DK (1) DK1248618T3 (https=)
ES (1) ES2259295T3 (https=)
PT (1) PT1248618E (https=)
WO (1) WO2001037833A1 (https=)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH12001001175B1 (en) * 2000-05-26 2006-08-10 Merck Sharp & Dohme 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl- (2,3')bipyridinyl in pure crystalline form and process for synthesis
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
WO2005085199A1 (en) * 2004-01-14 2005-09-15 Cadila Healthcare Limited Novel polymorphs of etoricoxib
PL2479166T3 (pl) 2009-02-27 2014-11-28 Cadila Healthcare Ltd Sposób otrzymywania etorykoksybu
WO2012163839A1 (en) 2011-05-27 2012-12-06 Farma Grs, D.O.O. A process for the preparation of polymorphic form i of etoricoxib
EP2773618A1 (en) 2011-11-03 2014-09-10 Cadila Healthcare Limited An improved process for the preparation of etoricoxib and polymorphs thereof
WO2013075732A1 (en) 2011-11-21 2013-05-30 Synthon Bv Process for making crystalline form i of etoricoxib
EP2601952A1 (en) 2011-12-07 2013-06-12 Zentiva, k.s. Novel pharmaceutically acceptable salts and cocrystals of 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl and their therapeutic uses
EP2831045A2 (en) * 2012-03-30 2015-02-04 Mylan Laboratories, Limited An improved process for the preparation of etoricoxib
EP2888231B1 (en) 2012-08-27 2019-01-09 Glenmark Pharmaceuticals Limited Process for preparation of crystalline etoricoxib
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 (en) 2013-09-13 2015-03-19 Synthon B.V. Process for making etoricoxib
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
MX2018013070A (es) 2017-12-29 2019-10-15 Gruenenthal Gmbh Combinación farmacéutica que comprende clorhidrato de tramadol de liberación extendida y etoricoxib de liberación inmediata, y su uso para el tratamiento del dolor.
CN111410629A (zh) * 2020-03-31 2020-07-14 天津大学 依托考昔溶剂化物及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5321033A (en) 1991-11-15 1994-06-14 Merck Frosst Canada, Inc. Amorphous (quinolin-2-ylmethoxy)indole compounds useful for treating inflammatory diseases
IL127441A (en) 1996-07-18 2003-02-12 Merck Frosst Canada Inc Substituted pyridines, pharmaceutical compositions comprising them and their use in the preparation of anti-inflammatory medicaments or as selective cyclooxygenase-2 inhibitors
US5861419A (en) * 1996-07-18 1999-01-19 Merck Frosst Canad, Inc. Substituted pyridines as selective cyclooxygenase-2 inhibitors
US6127545A (en) 1997-04-18 2000-10-03 Merck & Co., Inc. Process for making 2-aryl-3-aryl-5-halo pyridines useful as COX-2 inhibitors
US6130334A (en) 1998-04-15 2000-10-10 Merck & Co., Inc. Process for making 2-aryl-3-aryl-5-halo pyridines useful as COX-2 inhibitors
US6040450A (en) 1997-09-25 2000-03-21 Merck & Co., Inc. Process for making diaryl pyridines useful as cox-2-inhibitors
HU227627B1 (en) * 1998-04-24 2011-10-28 Merck Sharp & Dohme Process for synthesizing pyridine derivatives as cox-2 inhibitors and the intermediates
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
PH12001001175B1 (en) * 2000-05-26 2006-08-10 Merck Sharp & Dohme 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl- (2,3')bipyridinyl in pure crystalline form and process for synthesis

Also Published As

Publication number Publication date
US6441002B1 (en) 2002-08-27
EP1248618A4 (en) 2003-05-14
JP4425514B2 (ja) 2010-03-03
AU776544B2 (en) 2004-09-16
US20030144327A1 (en) 2003-07-31
ATE320809T1 (de) 2006-04-15
US20020198238A1 (en) 2002-12-26
EP1248618A1 (en) 2002-10-16
CA2391650A1 (en) 2001-05-31
DE60026877T2 (de) 2006-11-23
AU1803101A (en) 2001-06-04
WO2001037833A1 (en) 2001-05-31
CA2391650C (en) 2011-01-25
DK1248618T3 (da) 2006-07-10
JP2003514859A (ja) 2003-04-22
DE60026877D1 (de) 2006-05-11
EP1248618B1 (en) 2006-03-22
PT1248618E (pt) 2006-07-31

Similar Documents

Publication Publication Date Title
ES2259295T3 (es) Formas polimorficas, amorfas e hidratadas de 5-cloro-3-(4-metanosulfonilfenil)-6'-metil-(2,3')bipiridinilo.
TW593315B (en) Substituted pyridines and pyridazines with angiogenesis inhibiting activity
JP7010851B2 (ja) N-(5-(3-(7-(3-フルオロフェニル)-3H-イミダゾ[4,5-c]ピリジン-2-イル)-1H-インダゾール-5-イル)ピリジン-3-イル)-3-メチルブタンアミドを調製するための方法
RU2303598C2 (ru) Полиморфные формы гидрохлорида 1-[4-(5-цианоиндол-3-ил)бутил]-4-(2-карбамоилбензофуран-5-ил)пиперазина
WO2023284537A1 (en) Kras g12d inhibitors and uses thereof
ES2750676T5 (en) Crystalline dihydrochloride hydrate salt of omecamtiv mecarbil and process for its preparation
ES2542425T3 (es) Pirrolo[1,2-b]pirazol piridinoquinoleino substituido monohidrato como inhibidor del TBF-beta
ES2351958T3 (es) 5-cloro-3-(4-metanosulfonilfenil)-6'-metil-[2,3'] bipiridinil en forma cristalina pura y procedimiento de síntesis.
KR102142797B1 (ko) 피리디닐아미노피리미딘 유도체의 메실레이트 염의 결정질 형태, 그의 제조 방법, 및 그의 용도
CN107759602A (zh) 含有共轭联烯结构的化合物、其药物组合物和用途
JP2019509308A (ja) 1−(5−(2,4−ジフルオロフェニル)−1−((3−フルオロフェニル)スルホニル)−4−メトキシ−1h−ピロール−3−イル)−n−メチルメタンアミン塩の新規な結晶形
KR102496869B1 (ko) 이미다조[1,2-a]피리딘 화합물의 신규 염, 이의 결정형 및 제조방법
CA2767992C (en) 2 - [[[2 -[(hydroxyacetyl) amino]- 4 -pyridinyl] methyl] thio]- n -[4 - (trifluoromethoxy) phenyl]- 3 -pyridinecarboxamide benzenesulfonate, crystal of same, crystal polymorph thereof, and methods for production thereof
CN121889396A (zh) 用于治疗甲状腺眼病的林西替尼的结晶盐
TW200808317A (en) Compounds for treating pulmonary hypertension
US9255063B2 (en) Colchicine solid-state forms; methods of making; and methods of use thereof
US20030153600A1 (en) 5-chloro-3-(4-methanesulfonylphenyl)-6'-methyl-[2,3']bipyridinyl in pure crystalline form and process for synthesis
US6858631B1 (en) Polymorphic, amorphous and hydrated forms of 5-chloro-3-(4-methanesulfonylphenyl)-6′-methyl-[2,3′]bipyridinyl
CN107573302B (zh) 芳基哌嗪化合物及其制备方法和用途
JP6985137B2 (ja) スルホンアミド化合物の結晶形
CN103819461B (zh) N-[3-氯-4-(3-氟苄氧基)苯基]-6-[5-[[2-(甲亚磺酰基)乙基]氨基]甲基]-2-呋喃基]-4-喹唑啉胺多晶型物及其制备方法
IL305788A (en) A crystalline salt of a multityrosine kinase inhibitor, a method for its preparation and its use
KR20260002254A (ko) 이미다조[1,2-a]피리딘 화합물의 신규 염의 결정형 및 이의 제조방법
KR20260002253A (ko) 이미다조[1,2-a]피리딘 화합물의 신규 염 및 이의 제조방법
ES3038762A1 (es) Procedimiento de síntesis de ácido 5-metoxi-2-(2H-1,2,3-triazol-2yl)benzoico, sal sódica de dicho ácido como intermedio de síntesis y uso del ácido o de su sal en la preparación de daridorexant y ciertos intermedios en la síntesis del mismo