ATE142494T1 - 2-arylthiazolderivat sowie dieses enthaltendes arzneimittel - Google Patents

2-arylthiazolderivat sowie dieses enthaltendes arzneimittel

Info

Publication number
ATE142494T1
ATE142494T1 AT91920699T AT91920699T ATE142494T1 AT E142494 T1 ATE142494 T1 AT E142494T1 AT 91920699 T AT91920699 T AT 91920699T AT 91920699 T AT91920699 T AT 91920699T AT E142494 T1 ATE142494 T1 AT E142494T1
Authority
AT
Austria
Prior art keywords
arylthiazole
product containing
medicinal product
alkyl
optionally protected
Prior art date
Application number
AT91920699T
Other languages
English (en)
Inventor
Shiro Kondo
Hisashi Fukushima
Masaichi Hasegawa
Masahiro Tsuchimoto
Ikuo Nagata
Yoshio Osada
Keiji Komoriya
Hisao Yamaguchi
Original Assignee
Teijin Ltd
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 Teijin Ltd filed Critical Teijin Ltd
Application granted granted Critical
Publication of ATE142494T1 publication Critical patent/ATE142494T1/de

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • 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
    • 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
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • 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
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D277/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/10Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Residential Or Office Buildings (AREA)
AT91920699T 1990-11-30 1991-11-29 2-arylthiazolderivat sowie dieses enthaltendes arzneimittel ATE142494T1 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP33014790 1990-11-30
JP21658691 1991-08-02

Publications (1)

Publication Number Publication Date
ATE142494T1 true ATE142494T1 (de) 1996-09-15

Family

ID=26521514

Family Applications (1)

Application Number Title Priority Date Filing Date
AT91920699T ATE142494T1 (de) 1990-11-30 1991-11-29 2-arylthiazolderivat sowie dieses enthaltendes arzneimittel

Country Status (13)

Country Link
US (1) US5614520A (de)
EP (1) EP0513379B1 (de)
JP (1) JP2725886B2 (de)
KR (1) KR100221041B1 (de)
AT (1) ATE142494T1 (de)
AU (1) AU645867B2 (de)
CA (1) CA2073981C (de)
DE (2) DE69122084T2 (de)
DK (1) DK0513379T3 (de)
ES (1) ES2092580T3 (de)
HU (1) HU218942B (de)
SG (1) SG86971A1 (de)
WO (1) WO1992009279A1 (de)

Families Citing this family (148)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5294630A (en) * 1992-07-07 1994-03-15 Eli Lilly And Company Treatment of inflammatory bowel disease
US5436258A (en) * 1992-09-09 1995-07-25 Eli Lilly And Company Prevention of bone resorption
EP0695742A1 (de) 1994-08-03 1996-02-07 Hoechst Aktiengesellschaft Fullerenazirin-Derivate, Verfahren zu ihrer Herstellung und deren Verwendung
US5843969A (en) * 1995-04-07 1998-12-01 Teijin Limited Protecting agent for organ or tissue
KR970061878A (ko) * 1996-02-23 1997-09-12 성재갑 신규한 아릴티아졸 유도체, 그의 제조방법 및 그를 유효성분으로 하는 제초제 조성물
US6156748A (en) * 1996-10-07 2000-12-05 Eli Lilly And Company Compounds useful as neuro-protective agents
US6472387B1 (en) 1996-10-07 2002-10-29 Eli Lilly And Company Methods of using compounds as neuro-protective agents
ID21775A (id) * 1996-10-25 1999-07-22 Yoshitomi Pharmaceutical Senyawa-senyawa 1-fenilpirazol dan penggunaan farmasinya
JP2001519341A (ja) 1997-10-06 2001-10-23 イーライ・リリー・アンド・カンパニー 神経保護剤として有用な新規化合物
JP3547707B2 (ja) * 1998-06-19 2004-07-28 帝人株式会社 2−(3−シアノ−4−イソブチルオキシフェニル)−4−メチル−5−チアゾールカルボン酸の結晶多形体およびその製造方法
US6083966A (en) 1998-08-31 2000-07-04 University Of Florida Thiazoline acid derivatives
EP1143951A3 (de) 1998-09-21 2002-02-06 University Of Florida Research Foundation, Inc. Mittel gegen malaria
US6410562B1 (en) 1998-12-18 2002-06-25 Eli Lilly And Company Hypoglycemic imidazoline compounds
US6348324B1 (en) 1999-01-21 2002-02-19 Hypoguard America Limited Composition and device for detecting leukocytes in urine
US6528652B1 (en) 1999-01-21 2003-03-04 Chronimed Composition and device for detecting leukocytes in urine
AU2001259758A1 (en) * 2000-05-12 2001-11-26 Immunex Corporation Interleukin-1 inhibitors in the treatment of diseases
DE10106852A1 (de) 2001-02-14 2002-09-05 T Luger Entzündungshemmende Verbindungen
JP4917243B2 (ja) * 2001-05-23 2012-04-18 日本曹達株式会社 チアゾール化合物の製造方法
WO2003082279A1 (en) 2002-03-28 2003-10-09 Teijin Limited Solid preparation containing single crystal form
US7273866B2 (en) * 2002-12-20 2007-09-25 Bristol-Myers Squibb Company 2-aryl thiazole derivatives as KCNQ modulators
US6933308B2 (en) * 2002-12-20 2005-08-23 Bristol-Myers Squibb Company Aminoalkyl thiazole derivatives as KCNQ modulators
US20040122067A1 (en) * 2002-12-20 2004-06-24 Lin Zhao Treatment of chronic heart failure
US7208514B2 (en) 2003-03-13 2007-04-24 Mitsubishi Pharma Corporation Tumorigenesis inhibitor
US20050027128A1 (en) * 2003-07-30 2005-02-03 Robbins Timothy A. Substituted thiazoles
AU2003270473A1 (en) 2003-09-09 2005-04-27 University Of Florida Desferrithiocin derivatives and their use as iron chelators
US7037927B2 (en) 2003-10-16 2006-05-02 Abbott Laboratories Amides that inhibit vanilloid receptor subtype 1 (VR1) receptor
US7485657B2 (en) * 2004-05-12 2009-02-03 Boehringer Ingelheim Pharmaceuticals, Inc. Anti-cytokine heterocyclic compounds
JP4914210B2 (ja) * 2004-06-14 2012-04-11 日本ケミファ株式会社 縮合ピリミジン誘導体、及びキサンチンオキシダーゼ阻害剤
WO2006022375A1 (ja) 2004-08-27 2006-03-02 Astellas Pharma Inc. 2-フェニルチオフェン誘導体
US7820700B2 (en) 2004-08-27 2010-10-26 Astellas Pharma Inc. 2-phenylpyridine derivative
EP1812071A2 (de) * 2004-10-13 2007-08-01 PTC Therapeutics, Inc. Verbindungen zur nonsense-unterdrückung und verwendung dieser verbindungen für die herstellung eines medikaments zur behandlung somatischer mutationsbedingter erkrankungen
US7790720B2 (en) 2005-03-31 2010-09-07 Ucb Pharma, S.A. Compounds comprising an oxazole or thiazole moiety, processes for making them, and their uses
MX2007012226A (es) 2005-04-04 2007-12-10 Univ Florida Analogos de polieter de desferritiocina.
WO2006121995A2 (en) * 2005-05-09 2006-11-16 Tap Pharmaceutical Products, Inc. Methods for treating nephrolithiasis
JP2009501721A (ja) * 2005-07-12 2009-01-22 アカディア ファーマシューティカルズ インコーポレイテッド レチノイン酸受容体における活性を伴う化合物
US20070167454A1 (en) * 2005-08-03 2007-07-19 Christopher Lademacher Methods for treating hypertension
CA2623327A1 (en) * 2005-10-07 2007-04-19 Kissei Pharmaceutical Co., Ltd. Nitrogenated heterocyclic compound and pharmaceutical composition comprising the same
WO2007043457A1 (ja) * 2005-10-07 2007-04-19 Astellas Pharma Inc. トリアリールカルボン酸誘導体
CN1954814A (zh) * 2005-10-26 2007-05-02 重庆医药工业研究院有限责任公司 一种具有协同作用治疗痛风的药物组合物及其制备方法
CN100430055C (zh) * 2005-11-11 2008-11-05 天津泰普药品科技发展有限公司 2-(3-氰基-4-异丁氧基苯基)-4-甲基-5-噻唑甲酸和聚乙烯吡咯烷酮玻璃态固溶体及其制备方法
MX2008010646A (es) * 2006-02-24 2008-10-14 Astellas Pharma Inc Agente para tratar o prevenir ulcera digestiva.
EP2030974B1 (de) * 2006-06-13 2016-02-17 Shanghai Institute of Materia Medica, Chinese Academy of Sciences Thiazol- nichtnukleosid-verbindungen, ihre herstellung, pharmazeutische zusammensetzung und ihre verwendung als antivirale mittel
CA2658342A1 (en) * 2006-07-19 2008-01-24 Nippon Medical School Foundation Therapeutic agent for amyotrophic lateral sclerosis
CN101812035B (zh) * 2006-09-07 2012-03-21 上海医药工业研究院 2-(3-氰基-4-异丁氧基苯基)-4-甲基-5-噻唑甲酸晶型及其制备方法
CN101139325B (zh) * 2006-09-07 2010-05-12 上海医药工业研究院 2-(3-氰基-4-异丁氧基苯基)-4-甲基-5-噻唑甲酸晶型及其制备方法
US20090124623A1 (en) * 2006-11-13 2009-05-14 Christopher Lademacher Methods for preserving and/or increasing renal function using xanthine oxidoreductase inhibitors
KR20150024919A (ko) * 2006-11-13 2015-03-09 다케다 파마슈티칼스 유에스에이, 인코포레이티드 크산틴 옥시도리덕타아제 억제제를 사용하여 신장 기능을 보존하는 방법
CN102093308B (zh) * 2006-12-07 2012-08-29 重庆医药工业研究院有限责任公司 非布司他的晶型及其制备方法
CN102093309B (zh) * 2006-12-07 2012-07-04 重庆医药工业研究院有限责任公司 非布司他的晶型及其制备方法
CN1970547B (zh) * 2006-12-07 2011-04-06 重庆医药工业研究院有限责任公司 非布司他的晶型及其制备方法
AU2008206231A1 (en) * 2007-01-19 2008-07-24 Takeda Pharmaceuticals U.S.A., Inc. Methods for preventing or reducing the number of gout flares using xanthine oxidoreductase inhibitors and anti-inflammatory agents
WO2008115433A1 (en) 2007-03-15 2008-09-25 University Of Florida Desferrithiocin polyether analogues
WO2008126772A1 (ja) * 2007-04-05 2008-10-23 Astellas Pharma Inc. 高血圧治療剤
EP2786993B1 (de) 2007-08-13 2017-11-15 Monsanto Technology LLC Zusammensetzungen und Verfahren zur Kontrolle von Nematoden
CN102186824B (zh) * 2008-10-15 2014-03-12 橘生药品工业株式会社 稠环衍生物及其医药用途
JP5580204B2 (ja) * 2008-10-15 2014-08-27 キッセイ薬品工業株式会社 ビアリールイソニコチン酸誘導体及びその医薬用途
CN101759656B (zh) * 2008-12-12 2013-04-03 重庆医药工业研究院有限责任公司 非布司他新晶型及其制备方法
CN101768150B (zh) * 2009-01-05 2014-08-06 常州市第四制药厂有限公司 2-[3-氰基-4-异丁氧基苯基]-4-甲基噻唑-5-甲酸晶型及其制备方法
CN101781270B (zh) * 2009-01-20 2013-03-27 重庆医药工业研究院有限责任公司 一种高纯度的非布司他及其制备方法
US20100311756A1 (en) * 2009-01-22 2010-12-09 Takeda Pharmaceuticals North America, Inc. Methods for delaying the progression of at least one of cardiac hypertrophy, cardiac remodeling or left ventricular function or the onset of heart failure in subjects in need of treatment thereof
CN101475541B (zh) * 2009-02-09 2011-05-25 扬州哈泰克材料有限公司 4-甲基噻唑-5-羧酸的一种制备方法
US8952174B2 (en) 2009-02-27 2015-02-10 Teijin Pharma Limited Process for producing phenyl-substituted heterocyclic derivative through coupling using transition metal catalyst
CN101580495A (zh) * 2009-05-25 2009-11-18 沈阳药科大学 5-取代苯基-3-异噁唑甲酸及其酯类化合物、组合物及其制备方法
BRPI1011014A2 (pt) 2009-06-09 2019-09-24 Teijin Pharma Ltd método de produção.
DE202010017868U1 (de) 2009-06-10 2012-11-28 Teva Pharmaceutical Industries Ltd. Kristalline Formen von Febuxostat
EP2266966A1 (de) 2009-06-11 2010-12-29 Chemo Ibérica, S.A. Verfahren zur Herstellung von Febuxostat
CN101928259B (zh) * 2009-06-18 2012-10-03 南京海辰药业有限公司 2-芳基噻唑衍生物及其药物组合物
US9545445B2 (en) 2009-06-26 2017-01-17 Teijin Pharma Limited Therapeutic drug for hypertension or prehypertension
CN103936689B (zh) * 2009-07-17 2016-08-17 北京利乐生制药科技有限公司 2-[3-氰基-4-异丁氧基苯基]-4-甲基噻唑-5-甲酸晶型及其制备方法
EP2483256A1 (de) 2009-09-10 2012-08-08 Teva Pharmaceutical Industries Ltd. Verfahren zur herstellung von febuxostat
IT1395936B1 (it) * 2009-09-29 2012-11-02 Dipharma Francis Srl Sali di febuxostat
TWI423962B (zh) 2009-10-07 2014-01-21 Lg Life Sciences Ltd 有效作為黃嘌呤氧化酶抑制劑之新穎化合物、其製備方法及含該化合物之醫藥組成物
WO2011073617A1 (en) 2009-12-14 2011-06-23 Cipla Limited Processes for the preparation of febuxostat and salts thereof
WO2011080651A2 (en) 2009-12-31 2011-07-07 Ranbaxy Laboratories Limited Polymorphic forms of febuxostat
WO2011101867A2 (en) 2010-02-19 2011-08-25 Cadila Healthcare Limited Substantially pure salts of febuxostat and processes for preparation thereof
US20130012553A1 (en) * 2010-02-19 2013-01-10 Macdonald Patricia Methods for stabilizing joint damage in subjects using xanthine oxidoreductase inhibitors
CA2792036A1 (en) 2010-03-04 2011-09-09 Ranbaxy Laboratories Limited Polymorph of 2-[3-cyano-4-(2-methylpropoxy)phenyl]-4-methylthiazole-5-carboxylic acid
US8969582B2 (en) 2010-04-29 2015-03-03 Dr. Reddy's Laboratories Ltd. Preparation of febuxostat
IT1400311B1 (it) 2010-05-10 2013-05-24 Menarini Int Operations Lu Sa Associazione di inibitori della xantina ossidasi e antagonisti del recettore dell'angiotensina ii e loro uso.
IT1400310B1 (it) 2010-05-10 2013-05-24 Menarini Int Operations Lu Sa Associazione di inibitori della xantina ossidasi e statine e loro uso.
IT1400309B1 (it) 2010-05-10 2013-05-24 Menarini Int Operations Lu Sa Associazione di inibitori della xantina ossidasi e calcio antagonisti e loro uso.
IT1400609B1 (it) 2010-05-10 2013-06-14 Menarini Int Operations Lu Sa Associazione di inibitori della xantina ossidasi e metformina e loro uso.
PE20170306A1 (es) * 2010-06-16 2017-05-06 Takeda Pharmaceuticals Usa Inc Nuevas formas de dosificacion de liberacion modificada de un inhibidor de la xantina oxidorreductasa o de inhibidores de xantina oxidasa
AR081930A1 (es) 2010-06-16 2012-10-31 Ardea Biosciences Inc Compuestos de tioacetato
JP5709146B2 (ja) 2010-06-16 2015-04-30 アルデア バイオサイエンシーズ インク. フェニルチオ酢酸化合物、組成物、および、その使用方法
RU2013103366A (ru) 2010-06-25 2014-07-27 Тейдзин Фарма Лимитед Терапевтическое средство с замедленным высвобождением для гипертонии и почечной дисфункции
AR081267A1 (es) * 2010-07-13 2012-07-18 Interquim Sa Procedimiento de obtencion de la forma cristalina a del febuxostat
EP2598494B1 (de) 2010-07-30 2014-11-26 Ranbaxy Laboratories Limited Verbessertes verfahren zur herstellung von febuxostat
WO2012020272A2 (en) 2010-08-13 2012-02-16 EGIS GYÓGYSZERGYÁR Nyilvánosan Müködö Részvénytársaság New salts, polymorphs and solvates of a pharmaceutical active ingredient
AU2011294204B2 (en) 2010-08-27 2015-07-23 Teijin Limited Method for producing phenyl-substituted heterocyclic derivative by means of coupling method using a palladium compound
US20130172571A1 (en) 2010-09-08 2013-07-04 Natco Pharma Limited Process to prepare ethyl 4-methyl-2-(4-(2-methylpropyloxy)-3-cyanophenyl)-5-thiazolecarboxylate
JP5978216B2 (ja) 2010-09-10 2016-08-24 タケダ ファーマシューティカルズ ユー.エス.エー. インコーポレイティド テオフィリンとフェブキソスタットの併用療法のための方法
US20130303780A1 (en) 2010-11-08 2013-11-14 Siva Rama Prasad Vellanki Process for the preparation of 2-arylthiazole derivatives
WO2012073259A1 (en) 2010-12-02 2012-06-07 Indoco Remedies Limited Novel process for the preparation of febuxostat
WO2012098501A1 (en) 2011-01-21 2012-07-26 Ranbaxy Laboratories Limited Febuxostat co-crystals
WO2012109573A1 (en) * 2011-02-11 2012-08-16 Purdue Research Foundation Substituted thiazoles for use as antiviral agents
CN102643249A (zh) * 2011-02-18 2012-08-22 苏州波锐生物医药科技有限公司 2-芳基噻唑衍生物,其可药用盐及用途
WO2012131590A1 (en) 2011-03-31 2012-10-04 Sandoz Ag An improved process for preparation of febuxostat and its polymorphic crystalline form c thereof
AU2012241378A1 (en) 2011-04-15 2013-10-31 Sun Pharmaceutical Industries Limited Febuxostat solid dispersion
WO2012153313A1 (en) 2011-05-11 2012-11-15 Ranbaxy Laboratories Limited Pharmaceutical composition of febuxostat
WO2012172461A1 (en) 2011-06-13 2012-12-20 Ranbaxy Laboratories Limited Pharmaceutical compositions of febuxostat
WO2013050996A2 (en) * 2011-10-05 2013-04-11 Mapi Pharma Ltd. Process and intermediates for the preparation of substituted 2-arylthiazole carboxylic acids
TW201328692A (zh) * 2011-10-11 2013-07-16 Univ Osaka 脫髓鞘疾病之治療劑及預防劑
CA2852490A1 (en) 2011-11-03 2013-05-10 Ardea Biosciences, Inc. 3,4-di-substituted pyridine compound to reduce serum uric acid levels
CN104114545B (zh) * 2011-11-15 2018-06-01 迈兰实验室有限公司 用于制备非布索坦多晶型物的方法
BR112014014544A2 (pt) 2011-12-16 2017-06-13 Univ Florida usos de análogos de 4'-desferritiocina
WO2013088449A1 (en) 2011-12-16 2013-06-20 Natco Pharma Limited Stable crystal form of febuxostat and process for the preparation thereof
EP2606888A1 (de) * 2011-12-19 2013-06-26 Dompe' S.P.A. TRPM8-Antagonisten
ES2676884T3 (es) * 2011-12-19 2018-07-25 Dompé Farmaceutici S.P.A. Antagonistas de TRPM8
AU2013212865A1 (en) * 2012-01-27 2014-08-14 National University Corporation Tottori University Therapeutic agent for diabetes
EP2925306A1 (de) 2012-07-12 2015-10-07 Alembic Pharmaceuticals Limited Pharmazeutische zusammensetzung von febuxostat
EP2692342A1 (de) 2012-07-30 2014-02-05 Interquim, S.A. Verfahren zur Herstellung pharmazeutischer Zusammensetzungen mit Febuxostat in Tablettenform
CN103130744B (zh) * 2012-08-28 2014-10-15 沈阳药科大学 一种硒唑甲酸类化合物及其制备方法和用途
WO2014057461A1 (en) 2012-10-11 2014-04-17 Ranbaxy Laboratories Limited Process for the preparation of crystalline form g of febuxostat
RU2627591C2 (ru) * 2012-10-23 2017-08-09 Тейдзин Фарма Лимитед Терапевтический или профилактический агент для синдрома распада опухоли
CN103848798B (zh) * 2012-11-30 2016-01-06 镇江新元素医药科技有限公司 2-芳基硒唑化合物及其药物组合物
US8883857B2 (en) 2012-12-07 2014-11-11 Baylor College Of Medicine Small molecule xanthine oxidase inhibitors and methods of use
CN103936693B (zh) * 2013-01-22 2016-06-15 沈阳药科大学 2-(3-氰基-4-取代苯基)-4-甲基-1,3-硒唑-5-甲酸及其酯类化合物和制备方法
TWI606048B (zh) * 2013-01-31 2017-11-21 帝人製藥股份有限公司 唑苯衍生物
CN103333134B (zh) * 2013-03-01 2016-02-24 沈阳药科大学 2-(3-氰基-4-烷氧基)苯基-4-取代噻唑-5-甲酸类化合物、组合物及其制备方法和用途
CN104163782A (zh) * 2013-05-17 2014-11-26 重庆圣华曦药业股份有限公司 一种制备3,4-取代的硫代苯甲酰胺的方法及其在非布司他合成中的应用
WO2014192977A1 (ja) * 2013-05-31 2014-12-04 帝人ファーマ株式会社 チアゾール誘導体
ES2772131T3 (es) 2013-08-07 2020-07-07 Pharmathen Sa Un nuevo proceso para la preparación de Febuxostat
CN104418822B (zh) * 2013-08-22 2016-12-28 南京华威医药科技开发有限公司 具有黄嘌呤氧化酶抑制活性的化合物及其用途
CN103524456B (zh) * 2013-09-30 2016-06-01 南京华威医药科技开发有限公司 一种硒唑甲酸类化合物及其盐
WO2015077655A1 (en) 2013-11-22 2015-05-28 University Of Florida Research Foundation, Inc. Desferrithiocin analogs and uses thereof
EP2881116A1 (de) 2013-12-05 2015-06-10 Ranbaxy Laboratories Limited Febuxostatzusammensetzung
CA2948792A1 (en) * 2014-05-13 2015-11-19 Teijin Pharma Limited Novel crystalline polymorphs of pyridine derivative and method for producing the same
EP3157918B1 (de) 2014-06-23 2019-03-27 Dompé farmaceutici S.p.A. 2-aryl-4-hydroxy-1,3-thiazolderivate als trpm8-antagonisten zur behandlung von neuralgie, schmerzen, copd und asthma.
JP2017165653A (ja) * 2014-07-30 2017-09-21 帝人ファーマ株式会社 アゾールカルボン酸誘導体
KR20170033321A (ko) * 2014-07-30 2017-03-24 데이진 화-마 가부시키가이샤 아졸벤젠 유도체의 결정
US20170217948A1 (en) 2014-07-30 2017-08-03 Teijin Pharma Limited Xanthine oxidase inhibitor
CA2956553C (en) 2014-07-30 2023-03-21 Teijin Pharma Limited A 1h-1,2,3,4-tetrazole benzene derivative, crystalline forms thereof, and its use as a xanthine oxidase inhibitor
CZ27857U1 (cs) 2014-12-12 2015-02-23 Zentiva, K.S. Formulace obsahující tuhý roztok febuxostatu
EP3263109B1 (de) 2015-02-24 2020-06-17 National University Corporation Tottori University Arzneimittel zur prävention und/oder behandlung von demenz
US9809586B2 (en) 2015-03-28 2017-11-07 Wisconsin Alumni Research Foundation Inhibitors of collagen prolyl 4-hydroxylase
US10570104B2 (en) 2015-04-27 2020-02-25 University Of Florida Research Foundation, Incorporated Metabolically programmed metal chelators and uses thereof
EP3344604B1 (de) * 2015-09-02 2020-11-04 Sunshine Lake Pharma Co., Ltd. Carboxy-substituierte (hetero) aromatische ringderivate und herstellungsverfahren und verwendungen davon
EP3417858B8 (de) 2016-02-19 2020-12-30 National University Corporation Tottori University Therapeutikum oder prophylaktikum gegen demenz
CN106146419A (zh) * 2016-08-01 2016-11-23 沈阳药科大学 黄嘌呤氧化酶抑制剂
CN108358866B (zh) * 2017-01-12 2021-03-23 江西同和药业股份有限公司 一种非布司他中间体的制备方法及其在制备非布司他中的应用
CN110066258A (zh) 2018-01-23 2019-07-30 湘北威尔曼制药股份有限公司 噻唑-5-甲酸衍生物及其制备方法与应用
CN108484494B (zh) * 2018-06-15 2021-07-30 沈阳药科大学 2-氧代-1,2-二氢吡啶-4-甲酸类化合物
CN109810073B (zh) * 2019-02-28 2023-01-06 南京海辰药业股份有限公司 4-芳基噻唑衍生物及其药物组合物
CN114341120A (zh) 2019-08-21 2022-04-12 国立大学法人东京大学 Abcc11抑制剂
CN113024534B (zh) * 2019-12-24 2023-03-21 武汉光谷亚太医药研究院有限公司 2-吡啶基噻唑衍生物及其应用
CN115572272B (zh) * 2022-11-15 2024-05-07 湖北华世通生物医药科技有限公司 非布司他及其醛基酯类中间体的制备方法
WO2025221114A1 (ko) * 2024-04-17 2025-10-23 연세대학교 산학협력단 신규한 페북소스타트 유도체 및 이를 포함하는 염증성 질환의 예방 또는 치료용 조성물

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1516777A (fr) * 1966-08-02 1968-02-05 Innothera Lab Sa Dérivés du thiazole ainsi que de la thiazolo [4,5-d] pyridazine et leur préparation
CA962269A (en) * 1971-05-05 1975-02-04 Uniroyal Ltd. Thiazoles, and their use as insecticides
DE2125251A1 (en) * 1971-05-21 1972-11-30 Badische Anilin- & Soda-Fabrik Ag, 6700 Ludwigshafen Monoazo dispersion dyes - contg a thiazolyl substit in 2-position for use on synthetic fibres
DE2125193C3 (de) * 1971-05-21 1980-08-14 Basf Ag, 6700 Ludwigshafen 4-Nitro-2-thiazolyl-1 -aminobenzole und Verfahren zu ihrer Herstellung
US3852293A (en) * 1972-06-21 1974-12-03 Uniroyal Inc 4-phenyl-2-(3-pyridyl)-thiazole carboxamides
US4020080A (en) * 1974-07-01 1977-04-26 Eastman Kodak Company Oxadiazolylphenyl aromatic ester compounds and their use as ultraviolet stabilizer in organic compositions
US4363813A (en) * 1979-07-09 1982-12-14 Kureha Kagaku Kogyo Kabushiki Kaisha 2-(3,4,5-Trimethoxyphenyl)-4,5-disubstituted thiazoles
DE3002989A1 (de) * 1980-01-29 1981-07-30 Hoechst Ag, 6000 Frankfurt Hydroxyphenyl-thiazol, -thiazolin und -thiazolidin-carbonsaeuren, verfahren zu ihrer herstellung und ihre verwendung zur beeinflussung des kollagenstoffwechsels
US4346094A (en) * 1980-09-22 1982-08-24 Eli Lilly And Company 3-Aryl-5-isothiazolecarboxylic acids and related compounds used to lower uric acid levels
JPS5772975A (en) * 1980-10-24 1982-05-07 Kureha Chem Ind Co Ltd 2-substituted phenylthiazole derviative, and medicine for peptic ulcer containing said derivative as active component
DE3141430A1 (de) * 1981-10-19 1983-05-05 Basf Ag, 6700 Ludwigshafen Heterocyclisch substiutierte azofarbstoffe
US4571402A (en) * 1982-06-22 1986-02-18 Schering Corporation Anti-bronchoconstriction 2-(4'-pyridinyl)-thiazole derivatives, composition, and method of use therefor
US4528291A (en) * 1982-06-22 1985-07-09 Schering Corporation 2-(4'-Pyridinyl)-thiazole compounds and their use in increasing cardiac contractility
JPS5925381A (ja) * 1982-06-30 1984-02-09 Hisamitsu Pharmaceut Co Inc 新規なフエニル酢酸誘導体
JPH0725754B2 (ja) * 1986-01-30 1995-03-22 富山化学工業株式会社 新規なチアゾール化合物またはその塩
JPH01110683A (ja) * 1986-09-27 1989-04-27 Sawai Seiyaku Kk N−テトラゾリルチアゾールカルボキシアミド誘導体およびその用途
JPS63112572A (ja) * 1986-10-30 1988-05-17 Yamanouchi Pharmaceut Co Ltd 2(3h)−チアゾロン誘導体
JPS63112574A (ja) * 1986-10-30 1988-05-17 Yamanouchi Pharmaceut Co Ltd 4−トリ置換フエニル−2(3h)−チアゾロン誘導体
WO1990009381A1 (en) * 1989-02-08 1990-08-23 Abbott Laboratories 4-hydroxythiazoles as 5-lipoxygenase inhibitors
JPH02229190A (ja) * 1989-03-02 1990-09-11 Taisho Pharmaceut Co Ltd アゾール誘導体
US5244867A (en) * 1989-09-26 1993-09-14 Basf Aktiengesellschaft Oxazole- and thiazolecarboxamides

Also Published As

Publication number Publication date
JP2725886B2 (ja) 1998-03-11
HU9202265D0 (en) 1992-10-28
EP0513379B1 (de) 1996-09-11
DE69122084D1 (de) 1996-10-17
DE122008000051I1 (de) 2009-02-05
KR100221041B1 (ko) 1999-09-15
AU8952291A (en) 1992-06-25
AU645867B2 (en) 1994-01-27
CA2073981A1 (en) 1992-05-31
DK0513379T3 (da) 1996-09-30
WO1992009279A1 (fr) 1992-06-11
DE69122084T2 (de) 1997-04-03
KR927003052A (ko) 1992-12-17
HU218942B (hu) 2001-01-29
EP0513379A4 (en) 1993-09-01
SG86971A1 (en) 2002-03-19
EP0513379A1 (de) 1992-11-19
ES2092580T3 (es) 1996-12-01
CA2073981C (en) 2002-01-08
HUT63838A (en) 1993-10-28
US5614520A (en) 1997-03-25

Similar Documents

Publication Publication Date Title
ATE142494T1 (de) 2-arylthiazolderivat sowie dieses enthaltendes arzneimittel
ATE194335T1 (de) 4,5-diaryloxazol-derivate
DE69528005D1 (de) Prolineamid-Derivate
HUT65890A (en) Process for preparation of aromatic amidine derivatives and pharmaceutical compositions containing them
ATE150749T1 (de) Substituierte heterocyclische carbonsäureamide, ihre herstellung und ihre verwendung als arzneimittel
RU94040163A (ru) Гетероциклические производные карбоновой кислоты и их соли и фармацевтическая композиция с антифибротической или тормозящей пролилгидроксилазу или биосинтез коллагена активностью
ATE226574T1 (de) 4,6-diarylpyrimidin-derivate und deren salze
ATE227293T1 (de) 2,3-disubstituierte-(5,6)-heteroarylkondensiert - pyrimidin-4-one
HUP9802762A2 (hu) Difenil-metilén-piperidin-származékok, e vegyületeket tartalmazó gyógyászati készítmények, eljárás előállításukra és alkalmazásuk
NO306992B1 (no) Quinolinderivater, farmasoeytiske preparater inneholdende forbindelsene og anvendelsen av forbindelsene
NO923126D0 (no) Preparat og metode for behandling av canser
NO307464B1 (no) Galantaminderivater, farmasøytisk sammensetning inneholdende samme samt deres anvendelse for fremstilling av medikamenter
HU9300202D0 (en) Benzo-pyrane derivatives, pharmaceutical preparatives containing them as active substance as well as method for producing them
IL106993A (en) Benzenalkanoic acid derivatives and pharmaceutical compositions containing them
IL110894A0 (en) Cephem derivatives, processes for the preparation thereof, and pharmaceutical compositions containing the same
NO20020804D0 (no) Nye A-500359-derivater
DE69329184D1 (de) Alkylsubstituierte heterocyclische Verbindungen
AR029937A1 (es) Utilizacion de derivados de 2-aminotiazolina para la preparacion de medicamentos, derivados de 2-aminotiazolina y sus procedimientos de preparacion, las composiciones farmaceuticas que contienen dichos derivados, los compuestos intermediarios en la preparacion de dichos derivados y los procedimiento
DE69300318D1 (de) Flavonderivate.
DE69528984D1 (de) Hemmung der leukotrienbiosynthese mittels harnstoffderivaten
DE69401521D1 (de) Piperidin-Derivate mit antihistaminischer und antileukomenischer Wirkung
EP0601181A4 (en) Benzofuran derivative and pharmaceutical composition.

Legal Events

Date Code Title Description
EEIH Change in the person of patent owner
EELA Cancelled due to lapse of time