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TNSN03147A1 - Formes cristallines de sel de calcium (2 :1) d'acide [r-(r*,r*)]-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1-h-pyrrole-1-heptanoique (atorvastatine) - Google Patents

Formes cristallines de sel de calcium (2 :1) d'acide [r-(r*,r*)]-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1-h-pyrrole-1-heptanoique (atorvastatine)

Info

Publication number
TNSN03147A1
TNSN03147A1 TNPCT/IB2002/001796A TNSN03147A TNSN03147A1 TN SN03147 A1 TNSN03147 A1 TN SN03147A1 TN SN03147 A TNSN03147 A TN SN03147A TN SN03147 A1 TNSN03147 A1 TN SN03147A1
Authority
TN
Tunisia
Prior art keywords
atorvastatine
phenylamino
methylethyl
fluorophenyl
pyrrole
Prior art date
Application number
TNPCT/IB2002/001796A
Other languages
English (en)
Inventor
Stephen Robert Byrn
David Andrew Coates
Karen Sue Gushurst
Henry Grant Ii Morrison
Aeri Park
Petinka Ivanova Vlahova
Zheng Jane Li
Joseph Francis Krzyzaniak
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=23166039&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TNSN03147(A1) "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 TNSN03147A1 publication Critical patent/TNSN03147A1/fr

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/401—Proline; Derivatives thereof, e.g. captopril
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00—Drugs for skeletal disorders
    • A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Physical Education & Sports Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Rheumatology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Biomedical Technology (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Psychiatry (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

FORMES CRISTALLINES NOUVELLES DU SEL HEMICALCIQUE D'ACIDE [R-(R*,R*)]-2-(4-FLUOROPHENYL)- BETA - DIHYDROXY -5-(1-METHYLETHYL)-3-PHENYL-4-[(PHENYLAMINO)-CARBONYL]-1H-PYRROLE-1-HEPTANOدQUE (ATORVASTATINE), APPELEES FORME V, FORME VI, FORME VII, FORME VIII, FORME XIX, FORME X, FORME XI, FORME XII, FORME XIII, FORME XIV, FORME XV, FORME XVI, FORME XVII, FORME XVIII ET FORME XIX. CARACTERISEES PAR LEUR DIFFRACTION DES RAYONS X SUR POUDRE, RMN A L'ETAT SOLIDE ET/OU SPECTROSCOPIE RAMAN SONT DECRITES. TOUT COMME DES PROCEDES POUR LEUR PREPARATION ET DES COMPOSITIONS PHARMACEUTIQUES LES CONTENANT. UTILES COMME AGENTS POUR LE TRAITEMENT DE L'HYPERLIPIDEMIE, L'HYPERCHOLESTEROLEMIE, L'OSTEOPOROSE ET LA MALADIE D'ALZHEIMER.
TNPCT/IB2002/001796A 2001-06-29 2003-07-08 Formes cristallines de sel de calcium (2 :1) d'acide [r-(r*,r*)]-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1-h-pyrrole-1-heptanoique (atorvastatine) TNSN03147A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US30204901P 2001-06-29 2001-06-29

Publications (1)

Publication Number Publication Date
TNSN03147A1 true TNSN03147A1 (en) 2005-12-23

Family

ID=23166039

Family Applications (1)

Application Number Title Priority Date Filing Date
TNPCT/IB2002/001796A TNSN03147A1 (en) 2001-06-29 2003-07-08 Formes cristallines de sel de calcium (2 :1) d'acide [r-(r*,r*)]-2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1-h-pyrrole-1-heptanoique (atorvastatine)

Country Status (40)

Country Link
US (5) US6605729B1 (fr)
EP (2) EP1423364B1 (fr)
JP (2) JP3965155B2 (fr)
KR (1) KR100609371B1 (fr)
CN (2) CN101215253A (fr)
AP (1) AP1571A (fr)
AR (1) AR036118A1 (fr)
AU (1) AU2002258092B2 (fr)
BG (1) BG108393A (fr)
BR (1) BR0210666A (fr)
CA (1) CA2450111C (fr)
CR (2) CR7170A (fr)
CZ (1) CZ20033478A3 (fr)
DO (1) DOP2002000413A (fr)
EA (1) EA005317B1 (fr)
EC (1) ECSP034928A (fr)
EE (1) EE200300597A (fr)
ES (1) ES2558565T3 (fr)
GE (1) GEP20053546B (fr)
HR (1) HRP20031039A2 (fr)
HU (1) HUP0400381A2 (fr)
IL (1) IL158790A0 (fr)
MA (1) MA27044A1 (fr)
MX (1) MXPA03010266A (fr)
MY (1) MY122907A (fr)
NO (1) NO326170B1 (fr)
NZ (1) NZ529557A (fr)
OA (1) OA12636A (fr)
PA (1) PA8549501A1 (fr)
PE (1) PE20030124A1 (fr)
PL (1) PL367943A1 (fr)
RS (1) RS100003A (fr)
SK (1) SK16002003A3 (fr)
SV (1) SV2003001144A (fr)
TN (1) TNSN03147A1 (fr)
TW (1) TWI319396B (fr)
UA (1) UA74075C2 (fr)
UY (1) UY27359A1 (fr)
WO (1) WO2003004470A1 (fr)
ZA (1) ZA200308731B (fr)

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DE69634054T2 (de) 1995-07-17 2005-12-08 Warner-Lambert Co. Kristalline (R-(R*, R*))-2-(4-Fluorophenyl)-β, δ-Dihydroxy-5-(1-Methylethyl)-3-Phenyl-4-((Phenylamino)Carbonyl)-1H-Pyrrol-1-Heptancarbonsäure Hemi Calcium Salz (Atorvastatin)
WO1999026657A1 (fr) * 1997-11-25 1999-06-03 Musc Foundation For Research Development Inhibiteurs de la monoxyde d'azote-synthase
US20080275104A1 (en) * 1997-11-25 2008-11-06 Musc Foundation For Research Development Methods of treating juvenile type 1 diabetes mellitus
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US7411075B1 (en) 2000-11-16 2008-08-12 Teva Pharmaceutical Industries Ltd. Polymorphic form of atorvastatin calcium
PL362472A1 (en) * 2000-11-03 2004-11-02 Teva Pharma Atorvastatin hemi-calcium form vii
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
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
KR100790766B1 (ko) * 2000-12-27 2008-01-03 테바 파마슈티컬 인더스트리즈 리미티드 아토르바스타틴의 결정 형태, 이의 제조방법 및 이를 포함하는 약제학적 조성물
EP1423364B1 (fr) * 2001-06-29 2015-11-04 Warner-Lambert Company LLC Formes cristallines de sel hemicalcique (2:1) d'acide [r-(r*,r*)] -2-(4-fluorophenyl)-beta,delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-(phenylamino)carbonyl -1h-pyrrole-1-heptanoique (atorvastatine)
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IL163594A0 (en) * 2002-02-19 2005-12-18 Teva Pharma Processes for desolvating solvates of atorvastatinhemi-calcium and atorvastatin hemi-calcium essentially free of organic solvent
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EP1711197A4 (fr) * 2003-12-23 2008-11-05 Musc Found For Res Dev Methodes et compositions pour la prevention et le traitement de maladies ou de troubles inflammatoires
WO2005090301A1 (fr) * 2004-03-17 2005-09-29 Ranbaxy Laboratories Limited Forme cristalline d'hemi-calcium d'atorvastatine
SI1727795T1 (sl) 2004-03-17 2012-05-31 Ranbaxy Lab Ltd Postopek za pripravo atorvastatin kalcija v amorfni obliki
EP1745020A2 (fr) 2004-05-05 2007-01-24 Pfizer Products Incorporated Formes salines d'acide ¬r-(r*, r*)|-2-(4-fluorophenyl)-beta, delta-dihydroxy-5-(1-methylethyl)-3-phenyl-4-¬(phenylamino)carbonyl|-1h-pyrrole-1-heptanoique
MX2007000765A (es) * 2004-07-20 2007-03-28 Warner Lambert Co Formas cristalinas de sal de calcio del acido (r-(r*, r*))-2- (4-fluorofenil)- beta,gama- dihidroxi-5- (1-metiletil)-3 -fenil-4-((fenilamino) (carbonil)-1ih -pirrol-1- heptanoico (2:1).
EP1694685A1 (fr) * 2004-09-28 2006-08-30 Teva Pharmaceutical Industries Ltd Procede pour la preparation de formes du sel de calcium de l'atorvastatine substantiellement libres d'impuretees
KR20070067175A (ko) * 2004-10-28 2007-06-27 워너-램버트 캄파니 엘엘씨 무정형 아토르바스타틴 형성 방법
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CZ201039A3 (cs) 2010-01-19 2011-07-27 Zentiva, K. S Zpusob prumyslové výroby amorfní formy hemivápenaté soli (3R,5R) 7-[3-fenyl-4-fenylkarbamoyl-2-(4-fluorfenyl)-5-isopropylpyrrol-1-yl]-3,5-dihydroxyheptanové kyseliny (atorvastatinu) s vysokým specifickým povrchem a jeho použití v lékové forme
KR20120011249A (ko) 2010-07-28 2012-02-07 주식회사 경보제약 아토바스타틴 헤미칼슘염의 신규한 결정형, 이의 수화물, 및 그의 제조방법
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