HK1060572A1 - Preparation process of pyrrole-3-carboxylic acid phenylamide derivatices. - Google Patents
Preparation process of pyrrole-3-carboxylic acid phenylamide derivatices.Info
- Publication number
- HK1060572A1 HK1060572A1 HK04103610A HK04103610A HK1060572A1 HK 1060572 A1 HK1060572 A1 HK 1060572A1 HK 04103610 A HK04103610 A HK 04103610A HK 04103610 A HK04103610 A HK 04103610A HK 1060572 A1 HK1060572 A1 HK 1060572A1
- Authority
- HK
- Hong Kong
- Prior art keywords
- derivatices
- pyrrole
- carboxylic acid
- preparation process
- acid phenylamide
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/416—2,5-Pyrrolidine-diones 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 other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Pyrrole Compounds (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US26050501P | 2001-01-09 | 2001-01-09 | |
PCT/IB2001/002729 WO2002055519A2 (en) | 2001-01-09 | 2001-12-27 | Novel process for the synthesis of 5-(4-fluorophenyl)-1-[2-((2r, 4r)-4-hydroxy -6-oxo-tetrahydro-pyran-2-yl)-ethyl]-2-isopropyl-4-phenyl-1h-pyrrole-3-carboxylic acid phenylamide |
Publications (1)
Publication Number | Publication Date |
---|---|
HK1060572A1 true HK1060572A1 (en) | 2004-08-13 |
Family
ID=22989433
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK04103610A HK1060572A1 (en) | 2001-01-09 | 2004-05-21 | Preparation process of pyrrole-3-carboxylic acid phenylamide derivatices. |
HK06104433A HK1084114A1 (en) | 2001-01-09 | 2006-04-12 | Compounds for synthesizing intermediate useful in the preparation of atorvastatin |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HK06104433A HK1084114A1 (en) | 2001-01-09 | 2006-04-12 | Compounds for synthesizing intermediate useful in the preparation of atorvastatin |
Country Status (25)
Country | Link |
---|---|
US (7) | US6476235B2 (el) |
EP (1) | EP1353917B1 (el) |
JP (2) | JP4190285B2 (el) |
KR (3) | KR100677008B1 (el) |
CN (4) | CN100351252C (el) |
AR (1) | AR035680A1 (el) |
AT (1) | ATE358126T1 (el) |
BR (1) | BR0116739A (el) |
CA (1) | CA2432064C (el) |
CY (1) | CY1106590T1 (el) |
CZ (1) | CZ20031893A3 (el) |
DE (1) | DE60127583T2 (el) |
DK (1) | DK1353917T3 (el) |
ES (1) | ES2282200T3 (el) |
HK (2) | HK1060572A1 (el) |
HU (1) | HUP0302647A3 (el) |
IL (4) | IL156461A0 (el) |
MX (1) | MXPA03005284A (el) |
PL (1) | PL365283A1 (el) |
PT (1) | PT1353917E (el) |
RU (1) | RU2244714C1 (el) |
TW (1) | TWI293073B (el) |
WO (1) | WO2002055519A2 (el) |
YU (1) | YU49003A (el) |
ZA (1) | ZA200304684B (el) |
Families Citing this family (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7411075B1 (en) | 2000-11-16 | 2008-08-12 | Teva Pharmaceutical Industries Ltd. | Polymorphic form of atorvastatin calcium |
IL156055A0 (en) * | 2000-11-30 | 2003-12-23 | Teva Pharma | Novel crystal forms of atorvastatin hemi calcium and processes for their preparation as well as novel processes for preparing other forms |
US7501450B2 (en) * | 2000-11-30 | 2009-03-10 | Teva Pharaceutical Industries Ltd. | Crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
US6476235B2 (en) * | 2001-01-09 | 2002-11-05 | Warner-Lambert Company | Process for the synthesis of 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide |
EP1406860A1 (en) * | 2001-07-06 | 2004-04-14 | Teva Pharmaceutical Industries Limited | Process for the preparation of 7-amino syn 3,5-dihydroxy heptanoic acid derivatives via 6-cyano syn 3,5-dihydroxy hexanoic acid derivatives |
US20060020137A1 (en) * | 2001-11-29 | 2006-01-26 | Limor Tessler | Novel crystal forms of atorvastatin hemi-calcium and processes for their preparation as well as novel processes for preparing other forms |
AU2003247124A1 (en) * | 2002-08-06 | 2004-02-25 | Warner-Lambert Company Llc | Process for preparing 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy -6-oxo-tetrahydro-pyran-2-yl)ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide |
KR100765555B1 (ko) * | 2002-08-06 | 2007-10-09 | 워너-램버트 캄파니 엘엘씨 | 5-(4-플루오로페닐)-1-[2-((2r,4r)-4-히드록시-6-옥소-테트라히드로-피란-2-일)에틸]-2-이소프로필-4-페닐-1h-피롤-3-카르복실산 페닐아미드의 제조 방법 |
WO2004046105A2 (en) * | 2002-11-15 | 2004-06-03 | Teva Pharmaceutical Industries Ltd. | Synthesis of 3,5-dihydroxy-7-pyrrol-1-yl heptanoic acids |
KR100780984B1 (ko) * | 2003-04-14 | 2007-11-29 | 워너-램버트 캄파니 엘엘씨 | 5-(4-플루오로페닐)-1-[2-((2r,4r)-4-히드록시-6-옥소-테트라히드로-피란-2-일)에틸]-2-이소프로필-4-페닐-1h-피롤-3-카르복실산 페닐아미드의 제조 방법 |
US7166638B2 (en) | 2003-05-27 | 2007-01-23 | Nicox S.A. | Statin derivatives |
US7790197B2 (en) * | 2003-06-09 | 2010-09-07 | Warner-Lambert Company Llc | Pharmaceutical compositions of atorvastatin |
US7655692B2 (en) * | 2003-06-12 | 2010-02-02 | Pfizer Inc. | Process for forming amorphous atorvastatin |
US20040253305A1 (en) * | 2003-06-12 | 2004-12-16 | Luner Paul E. | Pharmaceutical compositions of atorvastatin |
US20050271717A1 (en) * | 2003-06-12 | 2005-12-08 | Alfred Berchielli | Pharmaceutical compositions of atorvastatin |
ES2443994T3 (es) * | 2003-06-13 | 2014-02-21 | Boehringer Ingelheim International Gmbh | Ligandos quirales para el uso en síntesis asimétricas |
MXPA06003003A (es) * | 2003-09-17 | 2006-06-23 | Warner Lambert Co | Formas cristalinas de acido [r-(r*, r*)]-2-(4- fluorofenil)-(, (-dihidroxi -5-(1- metiletil)-3 -fenil-4 -[(fenilamino) -carbonil]- 1h-pirrol -1-heptanoico. |
WO2005040087A1 (de) | 2003-10-24 | 2005-05-06 | Lonza Ag | Verfahren zur herstellung von 6,6,6-trihalo-3,5-dioxohexansäureestern |
US20050152323A1 (en) * | 2004-01-12 | 2005-07-14 | Vincent Bonnassieux | Plug-in Wi-Fi access point device and system |
SI21745A (sl) * | 2004-04-09 | 2005-10-31 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Polimorfi derivata 1-pirol-1-heptanojske kisline, intermediata za pripravo atorvastatina |
WO2005100313A1 (en) * | 2004-04-16 | 2005-10-27 | Pfizer Products Inc. | Process for forming amorphous atorvastatin calcium |
BRPI0510713A (pt) | 2004-05-05 | 2007-11-20 | Pfizer Prod Inc | formas de sal de ácido [r-(r*,r*)]-2-(4-fluorofenil)-beta, delta-diidróxi-5-(1-metiletil)-3-fenil-4-[(fenilamino)ca rbonil]-1h-pirrol-1- heptanóico |
CZ299175B6 (cs) * | 2004-06-17 | 2008-05-07 | Zentiva, A. S | Zpusob stanovení enantiomerní cistoty 2-(4-fluorfenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-fenyl-4[(fenylamino)-karbonyl]-1H-pyrrol-1-heptanové kyseliny a jejích solí |
EP1771455B1 (en) * | 2004-07-16 | 2016-05-11 | LEK Pharmaceuticals d.d. | Oxidative degradation products of atorvastatin calcium |
CA2701710C (en) | 2004-07-20 | 2013-08-27 | Warner-Lambert Company Llc | Novel forms of [r-(r*,r*)]-2-(4-fluorophenyl)-.beta.,.delta.-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrrole-1-heptanoic acid calcium salt (2:1) |
NZ552632A (en) * | 2004-07-30 | 2010-11-26 | Exelixis Inc | Pyrrole derivatives as pharmaceutical agents |
AU2005298383A1 (en) * | 2004-10-28 | 2006-05-04 | Warner-Lambert Company Llc | Process for forming amorphous atorvastatin |
EP1819319A1 (en) * | 2004-12-02 | 2007-08-22 | Warner-Lambert Company LLC | Pharmaceutical compositions of amorphous atorvastatin and process for preparing same |
WO2006067795A2 (en) * | 2004-12-23 | 2006-06-29 | Jubilant Organosys Limited | Novel polymorphic forms of atorvastatin lactone and process for preparing the same |
JP2008533128A (ja) * | 2005-03-14 | 2008-08-21 | ファイザー・サイエンス・アンド・テクノロジー・アイルランド・リミテッド | Paal−Knorr縮合を用いた、アトルバスタチン中間体の製造 |
EP1705175A1 (en) * | 2005-03-24 | 2006-09-27 | ratiopharm GmbH | Process for preparing C5 products and their use for Atorvastatin synthesis |
CA2547216A1 (en) | 2005-09-21 | 2007-03-21 | Renuka D. Reddy | Process for annealing amorphous atorvastatin |
DE602006014193D1 (de) | 2005-11-21 | 2010-06-17 | Warner Lambert Co | Neue formen von är-(r*,r*)ü-2-(4-fluorphenyl)-b,d-dihydroxy-5-(1-methylethyl)-3-phenyl-4-ä(phenylamino)carbonylü-1h-pyrrol-1-heptansäure-magnesium |
GB0523637D0 (en) * | 2005-11-21 | 2005-12-28 | Avecia Pharmaceuticals Ltd | Process and compounds |
WO2007131528A1 (en) * | 2006-05-15 | 2007-11-22 | Ratiopharm Gmbh | Process for preparing c5 intermediates and their use in the preparation of n-substituted pyrrole derivatives |
KR101069698B1 (ko) * | 2008-08-28 | 2011-10-04 | 한국화학연구원 | 광학 활성을 갖는 (4r, 6r)-6-(2-아미노에틸)-4-하이드록시-테트라하이드로피란-2-온 유도체의 제조방법 |
CN101429195B (zh) * | 2008-11-03 | 2010-12-15 | 华东师范大学 | 一种高纯度阿托伐他汀重要合成中间体的制备方法 |
SI2373609T1 (sl) | 2008-12-19 | 2013-12-31 | Krka, D.D., Novo Mesto | Uporaba amfifilnih spojin za kontrolirano kristalizacijo statinov in intermediatov statinov |
EP2327682A1 (en) | 2009-10-29 | 2011-06-01 | KRKA, D.D., Novo Mesto | Use of amphiphilic compounds for controlled crystallization of statins and statin intermediates |
EP2473515A4 (en) | 2009-09-04 | 2013-11-27 | Univ Toledo | PROCESS FOR PREPARING OPTICALLY PURE BETA LACTONS FROM ALDEHYDE AND COMPOSITIONS MADE THEREOF |
KR100986755B1 (ko) * | 2009-12-29 | 2010-10-08 | 김우진 | 노즐 회전장치 및 이를 갖는 분수 |
CN101892276B (zh) * | 2010-06-12 | 2012-11-21 | 郝志艳 | 一种阿托伐他汀钙化合物及其新方法 |
EP2616454B1 (en) | 2010-09-16 | 2015-04-15 | DSM Sinochem Pharmaceuticals Netherlands B.V. | Esters of hexanoic acids as intermediates for the preparation of atorvastatin |
BRPI1101952B1 (pt) * | 2011-04-25 | 2022-02-01 | Universidade Estadual De Campinas - Unicamp | Processo de obtenção de atorvastatina cálcica utilizando novos intermediários e atorvastatina assim obtida |
EP2726456A1 (en) | 2011-07-01 | 2014-05-07 | DSM Sinochem Pharmaceuticals Netherlands B.V. | Micronized crystals of atorvastatin hemicalcium |
WO2017137469A1 (en) * | 2016-02-11 | 2017-08-17 | Stichting Katholieke Universiteit | Novel class of compounds for the treatment of cardiovascular disease |
AU2018367119B2 (en) * | 2017-11-16 | 2023-05-11 | Syngenta Participations Ag | Process for the preparation of enantiomerically and diastereomerically enriched cyclobutane amines and amides |
US10699269B1 (en) * | 2019-05-24 | 2020-06-30 | Blockstack Pbc | System and method for smart contract publishing |
US11657391B1 (en) | 2019-05-24 | 2023-05-23 | Hiro Systems Pbc | System and method for invoking smart contracts |
US11513815B1 (en) | 2019-05-24 | 2022-11-29 | Hiro Systems Pbc | Defining data storage within smart contracts |
CN113559318B (zh) * | 2021-07-05 | 2022-09-13 | 四川大学 | 一种促神经功能恢复的手性导电修复支架及其制备方法 |
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US4681893A (en) * | 1986-05-30 | 1987-07-21 | Warner-Lambert Company | Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis |
US5124482A (en) | 1988-02-22 | 1992-06-23 | Warner-Lambert Company | Process for trans-6-(2-substituted-pyrrol-1-yl)alkyl)pyran-2-one inhibitors of cholesterol synthesis |
US5245047A (en) | 1988-02-22 | 1993-09-14 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5149837A (en) | 1988-02-22 | 1992-09-22 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5216174A (en) * | 1988-02-22 | 1993-06-01 | Warner-Lambert Co. | Process for trans-6-[12-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
US5097045A (en) | 1989-02-01 | 1992-03-17 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
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FI94339C (fi) | 1989-07-21 | 1995-08-25 | Warner Lambert Co | Menetelmä farmaseuttisesti käyttökelpoisen /R-(R*,R*)/-2-(4-fluorifenyyli)- , -dihydroksi-5-(1-metyylietyyli)-3-fenyyli-4-/(fenyyliamino)karbonyyli/-1H-pyrroli-1-heptaanihapon ja sen farmaseuttisesti hyväksyttävien suolojen valmistamiseksi |
US5103024A (en) | 1990-10-17 | 1992-04-07 | Warner-Lambert Company | Process for the synthesis of (4r-cis)-1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate |
US5248793A (en) | 1990-10-17 | 1993-09-28 | Warner-Lambert Company | Process for the synthesis of (4R-cis)-1,1-dimethylethyl 6-iodomethyl or 6-(phenyl-substituted)sulfonyloxymethyl-2,2-dimethyl-1,3-dioxane-4-acetate |
US5155251A (en) | 1991-10-11 | 1992-10-13 | Warner-Lambert Company | Process for the synthesis of (5R)-1,1-dimethylethyl-6-cyano-5-hydroxy-3-oxo-hexanoate |
US5298627A (en) | 1993-03-03 | 1994-03-29 | Warner-Lambert Company | Process for trans-6-[2-(substituted-pyrrol-1-yl)alkyl]pyran-2-one inhibitors of cholesterol synthesis |
ES2167587T3 (es) | 1995-07-17 | 2002-05-16 | Warner Lambert Co | Forma cristalina de la sal hemicalcica del acido (r-(r*,r*))-2-(4-fluorofenil)-beta,delta-dihidroxi-5-(1-metiletil)-3-fenil-4-((fenilamino)carbonil)-1h-pirrol-1-heptanoico (atorvastatina). |
HRP960313B1 (en) | 1995-07-17 | 2002-08-31 | Warner Lambert Co | Form iii crystalline (r- (r*, r*)-2- (4-fluorophenyl) -beta-delta-hydroxy-5-(1-methylethyl) -3-phenyl-4- ((phenylamino) carbonyl -1h-pyrrole-1-heptanoic acid calcium salt (2:1) |
AU2077897A (en) * | 1996-04-10 | 1997-10-29 | Warner-Lambert Company | Nonpeptide endothelin antagonists with increased water solubility |
US6087511A (en) | 1996-07-16 | 2000-07-11 | Warner-Lambert Company | Process for the production of amorphous [R-(R*,R*)]-2-(4-fluorophenyl)-β,δ-dihydroxy-5-(1-methylethyl )-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid) calcium salt (2:1) |
TR199900191T2 (xx) | 1996-07-29 | 1999-04-21 | Warner-Lambert Company | (S)-3,4-Dihidroksibutirik asitin korumal� esterlerinin sentezi i�in geli�tirilmi� proses. |
US6476235B2 (en) * | 2001-01-09 | 2002-11-05 | Warner-Lambert Company | Process for the synthesis of 5-(4-fluorophenyl)-1-[2-((2R,4R)-4-hydroxy-6-oxo-tetrahydro-pyran-2-yl)-ethyl]-2-isopropyl-4-phenyl-1H-pyrrole-3-carboxylic acid phenylamide |
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2001
- 2001-12-17 US US10/015,558 patent/US6476235B2/en not_active Expired - Fee Related
- 2001-12-27 ES ES01273081T patent/ES2282200T3/es not_active Expired - Lifetime
- 2001-12-27 KR KR1020067001883A patent/KR100677008B1/ko not_active IP Right Cessation
- 2001-12-27 CN CNB2005100056012A patent/CN100351252C/zh not_active Expired - Fee Related
- 2001-12-27 WO PCT/IB2001/002729 patent/WO2002055519A2/en active Application Filing
- 2001-12-27 DE DE60127583T patent/DE60127583T2/de not_active Expired - Fee Related
- 2001-12-27 BR BR0116739-1A patent/BR0116739A/pt not_active IP Right Cessation
- 2001-12-27 CN CNA2006101518437A patent/CN101024626A/zh active Pending
- 2001-12-27 CN CNB018225098A patent/CN1222521C/zh not_active Expired - Fee Related
- 2001-12-27 CZ CZ20031893A patent/CZ20031893A3/cs unknown
- 2001-12-27 CA CA002432064A patent/CA2432064C/en not_active Expired - Fee Related
- 2001-12-27 RU RU2003120510/04A patent/RU2244714C1/ru active
- 2001-12-27 YU YU49003A patent/YU49003A/sh unknown
- 2001-12-27 AT AT01273081T patent/ATE358126T1/de not_active IP Right Cessation
- 2001-12-27 PL PL01365283A patent/PL365283A1/xx not_active Application Discontinuation
- 2001-12-27 HU HU0302647A patent/HUP0302647A3/hu unknown
- 2001-12-27 PT PT01273081T patent/PT1353917E/pt unknown
- 2001-12-27 IL IL15646101A patent/IL156461A0/xx unknown
- 2001-12-27 KR KR1020067022289A patent/KR100833911B1/ko not_active IP Right Cessation
- 2001-12-27 DK DK01273081T patent/DK1353917T3/da active
- 2001-12-27 MX MXPA03005284A patent/MXPA03005284A/es active IP Right Grant
- 2001-12-27 JP JP2002556188A patent/JP4190285B2/ja not_active Expired - Fee Related
- 2001-12-27 CN CNA2006101006335A patent/CN1907984A/zh active Pending
- 2001-12-27 EP EP01273081A patent/EP1353917B1/en not_active Expired - Lifetime
- 2001-12-27 KR KR1020037009159A patent/KR100582326B1/ko not_active IP Right Cessation
- 2001-12-28 TW TW090132903A patent/TWI293073B/zh active
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2002
- 2002-01-08 AR ARP020100043A patent/AR035680A1/es not_active Application Discontinuation
- 2002-07-18 US US10/198,682 patent/US6545153B1/en not_active Expired - Fee Related
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2003
- 2003-01-21 US US10/348,727 patent/US6933393B2/en not_active Expired - Fee Related
- 2003-06-17 ZA ZA200304684A patent/ZA200304684B/en unknown
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2004
- 2004-05-21 HK HK04103610A patent/HK1060572A1/xx not_active IP Right Cessation
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2005
- 2005-04-19 US US11/109,396 patent/US7183408B2/en not_active Expired - Fee Related
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2006
- 2006-04-12 HK HK06104433A patent/HK1084114A1/xx not_active IP Right Cessation
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2007
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- 2007-09-14 JP JP2007239659A patent/JP2008100989A/ja not_active Withdrawn
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2008
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Date | Code | Title | Description |
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CORR | Corrigendum |
Free format text: CORRECTED DATA OF SECTION 27 TO JOURNAL OF 20051223: [54] PREPARATION PROCESS OF PYRROLE-3-CARBOXYLIC ACID - PHENYLAMIDE DERIVATIVES |
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PC | Patent ceased (i.e. patent has lapsed due to the failure to pay the renewal fee) |
Effective date: 20091227 |