PL375415A1 - Sposób wytwarzania fenyloamidu kwasu 5-(4-fluorofenylo)-1-[2-((2R,4R)-4-hydroksy-6-okso-tetrahydropiran-2-ylo)-etylo]-2-izopropylo-4-fenylo-1H-pirolo-3-karboksylowego - Google Patents

Sposób wytwarzania fenyloamidu kwasu 5-(4-fluorofenylo)-1-[2-((2R,4R)-4-hydroksy-6-okso-tetrahydropiran-2-ylo)-etylo]-2-izopropylo-4-fenylo-1H-pirolo-3-karboksylowego

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Publication number
PL375415A1
PL375415A1 PL03375415A PL37541503A PL375415A1 PL 375415 A1 PL375415 A1 PL 375415A1 PL 03375415 A PL03375415 A PL 03375415A PL 37541503 A PL37541503 A PL 37541503A PL 375415 A1 PL375415 A1 PL 375415A1
Authority
PL
Poland
Prior art keywords
pyran
fluorophenyl
pyrrole
tetrahydro
oxo
Prior art date
Application number
PL03375415A
Other languages
English (en)
Inventor
Jade Douglas Nelson
Michael Gerard Pamment
Original Assignee
Warner-Lambert Company Llc
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 Warner-Lambert Company Llc filed Critical Warner-Lambert Company Llc
Publication of PL375415A1 publication Critical patent/PL375415A1/pl

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Classifications

    • 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
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hematology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyrrole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
PL03375415A 2002-08-06 2003-07-25 Sposób wytwarzania fenyloamidu kwasu 5-(4-fluorofenylo)-1-[2-((2R,4R)-4-hydroksy-6-okso-tetrahydropiran-2-ylo)-etylo]-2-izopropylo-4-fenylo-1H-pirolo-3-karboksylowego PL375415A1 (pl)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US40170702P 2002-08-06 2002-08-06

Publications (1)

Publication Number Publication Date
PL375415A1 true PL375415A1 (pl) 2005-11-28

Family

ID=31715723

Family Applications (1)

Application Number Title Priority Date Filing Date
PL03375415A PL375415A1 (pl) 2002-08-06 2003-07-25 Sposób wytwarzania fenyloamidu kwasu 5-(4-fluorofenylo)-1-[2-((2R,4R)-4-hydroksy-6-okso-tetrahydropiran-2-ylo)-etylo]-2-izopropylo-4-fenylo-1H-pirolo-3-karboksylowego

Country Status (19)

Country Link
US (3) US6777560B2 (pl)
EP (1) EP1534704B1 (pl)
JP (1) JP2005539018A (pl)
CN (1) CN100357289C (pl)
AR (1) AR040777A1 (pl)
AT (1) ATE368661T1 (pl)
AU (1) AU2003247124A1 (pl)
BR (1) BR0313246A (pl)
CA (1) CA2494269A1 (pl)
DE (1) DE60315308T2 (pl)
ES (1) ES2287549T3 (pl)
IL (1) IL166119A0 (pl)
MX (1) MXPA05001427A (pl)
PL (1) PL375415A1 (pl)
RS (1) RS20050105A (pl)
RU (1) RU2279430C2 (pl)
TW (1) TW200413358A (pl)
WO (1) WO2004014896A1 (pl)
ZA (1) ZA200500049B (pl)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
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ES2287549T3 (es) * 2002-08-06 2007-12-16 Warner-Lambert Company Llc Procedimiento para preparar la fenilamida del acido 5-(4-fluorofenil)-1-(2-((2r,4r)-4-hidroxi-6-oxo-tetrahidropiran-2-il)etil)-2-isopropil-4-fenil-1h-pirrol-3-carboxilico.
CN1774421A (zh) * 2003-04-14 2006-05-17 沃尼尔·朗伯有限责任公司 制备5－(4－氟苯基)－1－[2－((2r,4r)－4－羟基－6－氧代－四氢－吡喃－2－基)乙基]－2－异丙基－4－苯基－1h－吡咯－3－羧酸苯基酰胺的方法
NZ577031A (en) 2003-05-30 2010-09-30 Ranbaxy Lab Ltd Substituted pyrrole derivatives and their use as HMG-CO inhibitors
WO2007054896A1 (en) 2005-11-08 2007-05-18 Ranbaxy Laboratories Limited Process for (3r, 5r)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4- [(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3, 5-dihydroxy-heptanoic acid hemi calcium salt
JP4077863B1 (ja) 2007-05-31 2008-04-23 タヒボジャパン株式会社 抗癌活性を有する光学活性２−（１−ヒドロキシエチル）−５−ヒドロキシナフト［２，３−ｂ］フラン−４，９−ジオンの製法
CN101205209B (zh) * 2007-12-25 2010-06-02 浙江新东港药业股份有限公司 一种阿伐他汀中间体的精制方法
WO2011028309A1 (en) 2009-09-04 2011-03-10 University Of Toledo PROCESSES FOR PRODUCING OPTICALLY PURE β-LACTONES FROM ALDEHYDES AND COMPOSITIONS PRODUCED THEREBY
CN106083656B (zh) * 2016-06-20 2018-11-13 连云港笃翔化工有限公司 一种地瑞那韦关键中间体的合成方法
US12027979B2 (en) 2020-06-10 2024-07-02 Apple Inc. Battery path impedance compensation
CN116496496B (zh) * 2023-04-27 2024-11-05 中国石油大学(华东) 一种基于三嗪共价框架材料（CTFs）制备单位点催化剂的制备方法

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US509045A (en) * 1893-11-21 passburg
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
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
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
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
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
US5003080A (en) * 1988-02-22 1991-03-26 Warner-Lambert Company Process for trans-6-(2-(substituted-pyrrol-1-yl)alkyl)pryan-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
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
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)
JP3296564B2 (ja) * 1995-07-17 2002-07-02 ワーナー−ランバート・コンパニー 結晶性の〔Ｒ−（Ｒ▲上＊▼，Ｒ▲上＊▼）〕−２−（４−フルオロフェニル）−β，δ−ジヒドロキシ−５−（１−メチルエチル）−３−フェニル−４−〔（フェニルアミノ）カルボニル〕−１Ｈ−ピロール−１−ヘプタン酸ヘミカルシウム塩（アトルバスタチン）
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)
IL127058A (en) * 1996-07-29 2001-07-24 Warner Lambert Co Process for the synthesis of protected esters of acid (S) - 4,3 dehydroxybutyric
US6753443B1 (en) * 1999-10-18 2004-06-22 Samsung Fine Chemicals Co., Ltd. Preparing method of chiral ester
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
US6562201B2 (en) * 2001-06-08 2003-05-13 Applied Semiconductor, Inc. Semiconductive polymeric system, devices incorporating the same, and its use in controlling corrosion
ES2287549T3 (es) * 2002-08-06 2007-12-16 Warner-Lambert Company Llc Procedimiento para preparar la fenilamida del acido 5-(4-fluorofenil)-1-(2-((2r,4r)-4-hidroxi-6-oxo-tetrahidropiran-2-il)etil)-2-isopropil-4-fenil-1h-pirrol-3-carboxilico.

Also Published As

Publication number Publication date
HK1077825A1 (en) 2006-02-24
US20040068121A1 (en) 2004-04-08
DE60315308D1 (de) 2007-09-13
CN100357289C (zh) 2007-12-26
WO2004014896A1 (en) 2004-02-19
EP1534704A1 (en) 2005-06-01
RS20050105A (sr) 2007-11-15
MXPA05001427A (es) 2005-06-06
EP1534704B1 (en) 2007-08-01
US20060106228A1 (en) 2006-05-18
JP2005539018A (ja) 2005-12-22
AR040777A1 (es) 2005-04-20
IL166119A0 (en) 2006-01-15
RU2279430C2 (ru) 2006-07-10
AU2003247124A1 (en) 2004-02-25
ZA200500049B (en) 2006-07-26
CA2494269A1 (en) 2004-02-19
TW200413358A (en) 2004-08-01
ATE368661T1 (de) 2007-08-15
BR0313246A (pt) 2005-06-14
US7084282B2 (en) 2006-08-01
DE60315308T2 (de) 2007-12-20
ES2287549T3 (es) 2007-12-16
US20040220254A1 (en) 2004-11-04
US6777560B2 (en) 2004-08-17
RU2005102839A (ru) 2005-07-10
CN1675200A (zh) 2005-09-28

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