IL122161A - Process for the production of amorphous ÚR-(R*,R*)¾2-(4-fluorophenyl)-beta, delta, dihydroxy-5- (1-methylethyl)-3- phenyl-4- Ú(phenylamino) carbonyl¾-1H-pyrrole-1- heptanoic acid calcium salt - Google Patents

Process for the production of amorphous ÚR-(R*,R*)¾2-(4-fluorophenyl)-beta, delta, dihydroxy-5- (1-methylethyl)-3- phenyl-4- Ú(phenylamino) carbonyl¾-1H-pyrrole-1- heptanoic acid calcium salt

Info

Publication number
IL122161A
IL122161A IL12216196A IL12216196A IL122161A IL 122161 A IL122161 A IL 122161A IL 12216196 A IL12216196 A IL 12216196A IL 12216196 A IL12216196 A IL 12216196A IL 122161 A IL122161 A IL 122161A
Authority
IL
Israel
Prior art keywords
phenylamino
methylethyl
fluorophenyl
pyrrole
dihydroxy
Prior art date
Application number
IL12216196A
Other languages
English (en)
Other versions
IL122161A0 (en
Original Assignee
Warner Lambert Co
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=21696097&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IL122161(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Warner Lambert Co filed Critical Warner Lambert Co
Publication of IL122161A0 publication Critical patent/IL122161A0/xx
Publication of IL122161A publication Critical patent/IL122161A/xx

Links

Classifications

    • 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
    • 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
    • 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)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pyrrole Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
IL12216196A 1995-07-17 1996-07-16 Process for the production of amorphous ÚR-(R*,R*)¾2-(4-fluorophenyl)-beta, delta, dihydroxy-5- (1-methylethyl)-3- phenyl-4- Ú(phenylamino) carbonyl¾-1H-pyrrole-1- heptanoic acid calcium salt IL122161A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US145395P 1995-07-17 1995-07-17
PCT/US1996/011807 WO1997003960A1 (en) 1995-07-17 1996-07-16 NOVEL 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)

Publications (2)

Publication Number Publication Date
IL122161A0 IL122161A0 (en) 1998-04-05
IL122161A true IL122161A (en) 1999-07-14

Family

ID=21696097

Family Applications (1)

Application Number Title Priority Date Filing Date
IL12216196A IL122161A (en) 1995-07-17 1996-07-16 Process for the production of amorphous ÚR-(R*,R*)¾2-(4-fluorophenyl)-beta, delta, dihydroxy-5- (1-methylethyl)-3- phenyl-4- Ú(phenylamino) carbonyl¾-1H-pyrrole-1- heptanoic acid calcium salt

Country Status (37)

Country Link
US (1) US6274740B1 (cs)
EP (1) EP0839132B1 (cs)
JP (1) JP4064459B2 (cs)
KR (1) KR100400805B1 (cs)
CN (1) CN1087289C (cs)
AR (1) AR002849A1 (cs)
AT (1) ATE199542T1 (cs)
AU (1) AU700794B2 (cs)
BG (1) BG63631B1 (cs)
BR (1) BR9609714A (cs)
CA (1) CA2220455C (cs)
CO (1) CO4700441A1 (cs)
CZ (1) CZ289421B6 (cs)
DE (1) DE69611999T2 (cs)
DK (1) DK0839132T5 (cs)
EA (1) EA000625B1 (cs)
EE (1) EE03605B1 (cs)
ES (1) ES2156997T3 (cs)
GE (1) GEP20002027B (cs)
GR (1) GR3035859T3 (cs)
HR (1) HRP960312B1 (cs)
HU (1) HU220343B (cs)
IL (1) IL122161A (cs)
IN (1) IN185276B (cs)
MX (1) MX9708959A (cs)
NO (1) NO309322B1 (cs)
NZ (1) NZ313008A (cs)
PE (1) PE1698A1 (cs)
PL (1) PL191017B1 (cs)
PT (1) PT839132E (cs)
RO (1) RO120069B1 (cs)
SI (1) SI0839132T1 (cs)
SK (1) SK283204B6 (cs)
UA (1) UA50743C2 (cs)
UY (1) UY24286A1 (cs)
WO (1) WO1997003960A1 (cs)
ZA (1) ZA966043B (cs)

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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
IN191236B (cs) * 1999-05-25 2003-10-11 Ranbaxy Lab Ltd
HU226640B1 (en) * 1999-10-18 2009-05-28 Egis Gyogyszergyar Nyilvanosan Process for producing amorphous atorvastatin calcium salt
US6646133B1 (en) 2000-10-17 2003-11-11 Egis Gyogyszergyar Rt. Process for the preparation of amorphous atorvastatin calcium
US7411075B1 (en) 2000-11-16 2008-08-12 Teva Pharmaceutical Industries Ltd. Polymorphic form of atorvastatin calcium
SI20425A (sl) 1999-12-10 2001-06-30 LEK tovarna farmacevtskih in kemi�nih izdelkov d.d. Priprava amorfnega atorvastatina
KR100877165B1 (ko) * 2000-11-16 2009-01-07 테바 파마슈티컬 인더스트리즈 리미티드 수산화 칼슘을 이용한[Ｒ(Ｒ*,Ｒ*)]-2-(4-플루오로페닐)-β,δ-디하이드록시-5-(1-메틸에틸)-3-페닐-4-[(페닐아미노)카보닐]-1Ｈ-피롤-1-헵탄산 에스테르의 가수분해
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
NZ527048A (en) 2000-12-27 2004-12-24 Ciba Sc Holding Ag Crystalline forms of atorvastatin
WO2002057228A1 (en) * 2001-01-17 2002-07-25 Biocon India Limited Atorvastatin calcium
WO2002057229A1 (en) 2001-01-19 2002-07-25 Biocon India Limited FORM V CRYSTALLINE [R-(R*,R*)]-2-(4-FLUOROPHENYL)-ß,$G(D)-DIHYDROXY-5-(1-METHYLETHYL)-3-PHENYL-4-[(PHENYLAMINO)CARBONYL]-1H-PYRROLE-1- HEPTANOIC ACID HEMI CALCIUM SALT. (ATORVASTATIN)
SI20814A (sl) * 2001-01-23 2002-08-31 LEK, tovarna farmacevtskih in kemi�nih izdelkov, d.d. Priprava amorfnega atorvastatina
SI20848A (sl) * 2001-03-14 2002-10-31 Lek, Tovarna Farmacevtskih In Kemijskih Izdelkov, D.D. Farmacevtska formulacija, ki vsebuje atorvastatin kalcij
IN190564B (cs) * 2001-04-11 2003-08-09 Cadila Heathcare Ltd
GEP20053546B (en) 2001-06-29 2005-06-10 Warner Lambert Co Crystalline 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) (Atorvastatin)
US7361772B2 (en) 2001-08-16 2008-04-22 Biocon Limited Process for the production of atorvastatin calcium
US7563911B2 (en) 2001-08-31 2009-07-21 Morepen Laboratories Ltd. Process for the preparation of amorphous atorvastin calcium salt (2:1)
UA77990C2 (en) * 2001-12-12 2007-02-15 Crystalline calcium salt of (2:1) [r-(r*,r*)]-2-(4-fluorophenyl)-?,?-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrroleheptanic acid
CZ296967B6 (cs) * 2002-02-01 2006-08-16 Zentiva, A.S. Zpusob výroby amorfní formy hemivápenaté soli (3R,5R) 7-[3-fenyl-4-fenylkarbamoyl-2-(4-fluorfenyl)-5-isopropylpyrrol-1-yl]-3,5-dihydroxyheptanové kyseliny (atorvastatinu)
AU2002247944B2 (en) 2002-03-18 2009-05-21 Biocon Limited Amorphous Hmg-CoA reductase inhibitors of desired particle size
RU2309141C2 (ru) * 2002-03-18 2007-10-27 Байокон Лимитид АМОРФНЫЕ ИНГИБИТОРЫ ГМГ-КоА-РЕДУКТАЗЫ И СПОСОБ ИХ ПОЛУЧЕНИЯ
ITMI20020907A1 (it) * 2002-04-29 2003-10-29 Chemi Spa Processo di preparazione della forma amorfa del sale di calcio della atorvastatina
AU2002356423A1 (en) * 2002-05-28 2003-12-12 Cadila Healthcare Limited Process for the preparation of amorphous atorvastatin calcium
US7179942B2 (en) 2002-07-05 2007-02-20 Bicon Limited Halo-substituted active methylene compounds
AU2002330735A1 (en) * 2002-09-03 2004-03-29 Morepen Laboratories Limited Atorvastatin calcium form vi or hydrates thereof
AU2004228607B2 (en) * 2003-04-11 2011-01-27 Lek Pharmaceuticals D.D. Process for the preparation of amorphous calcium salt of atorvastatin
DK1631533T3 (da) 2003-04-22 2009-06-02 Biocon Ltd Hidtil ukendt fremgangsmåde til stereoselektiv reduktion af beta-ketoestre
US7790197B2 (en) * 2003-06-09 2010-09-07 Warner-Lambert Company Llc Pharmaceutical compositions of atorvastatin
US20050271717A1 (en) * 2003-06-12 2005-12-08 Alfred Berchielli 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
AU2003272080A1 (en) 2003-09-18 2005-04-06 Biocon Limited Novel process for the preparation of tert-butyl 6-cyano-5-hydroxy-3-oxohexanoate
CA2456430A1 (en) * 2004-01-28 2005-07-28 Brantford Chemicals Inc. Improved process for the preparation of amorphous atorvastatin calcium
CZ298382B6 (cs) * 2004-03-10 2007-09-12 Zentiva, A. S. Zpusob prípravy amorfní formy hemivápenaté soli atorvastatinu a její stabilizace
US7994343B2 (en) * 2004-03-17 2011-08-09 Ranbaxy Laboratories Limited Process for the production of atorvastatin calcium in amorphous form
EP1745020A2 (en) 2004-05-05 2007-01-24 Pfizer Products Incorporated Salt forms of atorvastatin
HUE029911T2 (en) * 2004-07-16 2017-04-28 Lek Pharmaceuticals Products of atorvastatin calcium oxidative degradation
JP2008510798A (ja) 2004-08-27 2008-04-10 バイオコン・リミテッド 非晶質アトルバスタチンカルシウムのための方法
WO2006039441A2 (en) * 2004-09-30 2006-04-13 Dr. Reddy's Laboratories Ltd. Amorphous atorvastatin calcium
TW200630335A (en) * 2004-10-18 2006-09-01 Teva Pharma Processes for preparing amorphous atorvastatin hemi-calcium
NZ554541A (en) * 2004-10-28 2011-01-28 Warner Lambert Co Process for forming amorphous atorvastatin
CA2588216A1 (en) * 2004-11-22 2006-05-26 Dexcel Pharma Technologies Ltd. Stable atorvastatin formulations
EP1819319A1 (en) * 2004-12-02 2007-08-22 Warner-Lambert Company LLC Pharmaceutical compositions of amorphous atorvastatin and process for preparing same
US20080108664A1 (en) * 2005-12-23 2008-05-08 Liu Belle B Solid-state form of AMG 706 and pharmaceutical compositions thereof
EP1810667A1 (en) 2006-01-20 2007-07-25 KRKA, tovarna zdravil, d.d., Novo mesto Pharmaceutical composition comprising amorphous atorvastatin
KR20070116963A (ko) * 2006-03-01 2007-12-11 테바 파마슈티컬 인더스트리즈 리미티드 아토르바스타틴 헤미 칼슘 결정형의 제조 방법
WO2008053312A2 (en) * 2006-11-02 2008-05-08 Cadila Pharmaceuticals Limited Process for preparing amorphous atorvastatin hemi calcium salt and its intermediate
US7834195B2 (en) 2007-01-24 2010-11-16 Apotex Pharmachem Inc. Atorvastatin calcium propylene glycol solvates
EP2185527A2 (en) * 2007-07-11 2010-05-19 Actavis Group PTC EHF Novel polymorph of atorvastatin calcium and use thereof for the preparation of amorphous atorvastatin calcium
US20090124817A1 (en) * 2007-11-09 2009-05-14 The Industry & Academic Cooperation In Chungnam National University Process for Preparing Amorphous Atorvastatin Calcium Nanoparticles
EP2075246A1 (en) 2007-12-27 2009-07-01 M. J. Institute of Research A process for preparation of amorphous form of atorvastatin hemi-calcium salt
WO2010066846A2 (en) * 2008-12-11 2010-06-17 Dsm Ip Assets B.V. Method for the isolation of atorvastatin
WO2010069593A1 (en) 2008-12-19 2010-06-24 Krka, D. D., Novo Mesto Use of amphiphilic compounds for controlled crystallization of statins and statin intermediates
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
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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
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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
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Also Published As

Publication number Publication date
HRP960312A2 (en) 1998-02-28
IN185276B (cs) 2000-12-16
JP4064459B2 (ja) 2008-03-19
RO120069B1 (ro) 2005-08-30
KR100400805B1 (ko) 2003-12-24
GR3035859T3 (en) 2001-08-31
UY24286A1 (es) 1997-01-17
DE69611999T2 (de) 2001-07-26
CA2220455A1 (en) 1997-02-06
JPH11510486A (ja) 1999-09-14
NZ313008A (en) 2000-01-28
UA50743C2 (uk) 2002-11-15
KR19990029045A (ko) 1999-04-15
AU700794B2 (en) 1999-01-14
DK0839132T5 (da) 2006-03-20
WO1997003960A1 (en) 1997-02-06
BR9609714A (pt) 1999-02-23
EE9700369A (et) 1998-06-15
CZ289421B6 (cs) 2002-01-16
HU220343B (hu) 2001-12-28
HK1018054A1 (en) 1999-12-10
SK283204B6 (sk) 2003-03-04
CN1087289C (zh) 2002-07-10
US6274740B1 (en) 2001-08-14
SI0839132T1 (cs) 2001-06-30
BG63631B1 (bg) 2002-07-31
EP0839132B1 (en) 2001-03-07
AR002849A1 (es) 1998-04-29
NO980209D0 (no) 1998-01-16
NO980209L (no) 1998-01-16
PL324463A1 (en) 1998-05-25
EA199800128A1 (ru) 1998-08-27
PL191017B1 (pl) 2006-03-31
HUP9903017A3 (en) 2001-01-29
SK5898A3 (en) 1998-08-05
AU6497896A (en) 1997-02-18
ZA966043B (en) 1997-02-03
MX9708959A (es) 1998-03-31
BG102188A (en) 1998-08-31
CO4700441A1 (es) 1998-12-29
EP0839132A1 (en) 1998-05-06
EE03605B1 (et) 2002-02-15
PE1698A1 (es) 1998-02-19
IL122161A0 (en) 1998-04-05
ES2156997T3 (es) 2001-08-01
DE69611999D1 (de) 2001-04-12
CZ12298A3 (cs) 1998-12-16
NO309322B1 (no) 2001-01-15
HRP960312B1 (en) 2001-10-31
DK0839132T3 (da) 2001-04-09
CA2220455C (en) 2002-09-24
EA000625B1 (ru) 1999-12-29
ATE199542T1 (de) 2001-03-15
PT839132E (pt) 2001-06-29
CN1190956A (zh) 1998-08-19
GEP20002027B (en) 2000-04-10

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NP Permission for amending the patent specification granted (section 66, patents law 1967)

Free format text: JOURNAL NO. 4/2001P. 1751, 1752, 1753 NOTICES PATENT APPLICATION NO. 122162, 122161, 122118 DELETE THE ABOVE NOTICES. THE NOTICES WERE PUBLISHED BEFORE PAYMENT OF PUBLICATION FEES. THE NOTICES ARE BEING REPUBLISHED IN THIS JOURNAL.

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