PL354604A1 - Process for the preparation of amorphous atorvastatin calcium - Google Patents
Process for the preparation of amorphous atorvastatin calciumInfo
- Publication number
- PL354604A1 PL354604A1 PL00354604A PL35460400A PL354604A1 PL 354604 A1 PL354604 A1 PL 354604A1 PL 00354604 A PL00354604 A PL 00354604A PL 35460400 A PL35460400 A PL 35460400A PL 354604 A1 PL354604 A1 PL 354604A1
- Authority
- PL
- Poland
- Prior art keywords
- atorvastatin calcium
- amorphous atorvastatin
- preparation
- amorphous
- crude
- Prior art date
Links
- OJRHUICOVVSGSY-RXMQYKEDSA-N (2s)-2-chloro-3-methylbutan-1-ol Chemical compound CC(C)[C@H](Cl)CO OJRHUICOVVSGSY-RXMQYKEDSA-N 0.000 title abstract 5
- 229960001770 atorvastatin calcium Drugs 0.000 title abstract 5
- 238000000034 method Methods 0.000 title abstract 2
- 238000002360 preparation method Methods 0.000 title abstract 2
- XUKUURHRXDUEBC-KAYWLYCHSA-N Atorvastatin Chemical compound C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CC[C@@H](O)C[C@@H](O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-KAYWLYCHSA-N 0.000 abstract 1
- XUKUURHRXDUEBC-UHFFFAOYSA-N Atorvastatin Natural products C=1C=CC=CC=1C1=C(C=2C=CC(F)=CC=2)N(CCC(O)CC(O)CC(O)=O)C(C(C)C)=C1C(=O)NC1=CC=CC=C1 XUKUURHRXDUEBC-UHFFFAOYSA-N 0.000 abstract 1
- 208000035150 Hypercholesterolemia Diseases 0.000 abstract 1
- 208000031226 Hyperlipidaemia Diseases 0.000 abstract 1
- 229960005370 atorvastatin Drugs 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000001816 cooling Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 238000001953 recrystallisation Methods 0.000 abstract 1
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
- A61P3/06—Antihyperlipidemics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HU9903634A HU226640B1 (en) | 1999-10-18 | 1999-10-18 | Process for producing amorphous atorvastatin calcium salt |
| PCT/HU2000/000106 WO2001028999A1 (en) | 1999-10-18 | 2000-10-17 | Process for the preparation of amorphous atorvastatin calcium |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL354604A1 true PL354604A1 (en) | 2004-01-26 |
Family
ID=90014241
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL00354604A PL354604A1 (en) | 1999-10-18 | 2000-10-17 | Process for the preparation of amorphous atorvastatin calcium |
Country Status (17)
| Country | Link |
|---|---|
| EP (1) | EP1235800B1 (cg-RX-API-DMAC7.html) |
| JP (1) | JP2003512354A (cg-RX-API-DMAC7.html) |
| KR (1) | KR100664353B1 (cg-RX-API-DMAC7.html) |
| CN (1) | CN1157374C (cg-RX-API-DMAC7.html) |
| AT (1) | ATE345327T1 (cg-RX-API-DMAC7.html) |
| AU (1) | AU1166301A (cg-RX-API-DMAC7.html) |
| CA (1) | CA2388018C (cg-RX-API-DMAC7.html) |
| CZ (1) | CZ300071B6 (cg-RX-API-DMAC7.html) |
| DE (1) | DE60031882T2 (cg-RX-API-DMAC7.html) |
| HR (1) | HRP20020334B1 (cg-RX-API-DMAC7.html) |
| HU (1) | HU226640B1 (cg-RX-API-DMAC7.html) |
| PL (1) | PL354604A1 (cg-RX-API-DMAC7.html) |
| RS (1) | RS50473B (cg-RX-API-DMAC7.html) |
| RU (1) | RU2255932C2 (cg-RX-API-DMAC7.html) |
| SK (1) | SK286861B6 (cg-RX-API-DMAC7.html) |
| UA (1) | UA72777C2 (cg-RX-API-DMAC7.html) |
| WO (1) | WO2001028999A1 (cg-RX-API-DMAC7.html) |
Families Citing this family (31)
| 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 |
| SI20425A (sl) * | 1999-12-10 | 2001-06-30 | LEK tovarna farmacevtskih in kemi�nih izdelkov d.d. | Priprava amorfnega atorvastatina |
| 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 |
| 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) |
| DE10135493A1 (de) * | 2001-07-20 | 2003-01-30 | Jobst Krauskopf | Pharmazeutische Zusammensetzung zur Behandlung von Hypercholesterinämie |
| AU2002255479B2 (en) | 2001-07-30 | 2008-09-11 | Dr. Reddy's Laboratories Ltd. | Crystalline forms VI and VII of atorvastatin clacium |
| HUP0500074A3 (en) * | 2002-03-18 | 2005-07-28 | Biocon Ltd Bangalore | Amorphous hmg-coa reductase inhibitors of desired particle size and process for producing them |
| 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 |
| WO2003099785A1 (en) * | 2002-05-28 | 2003-12-04 | Cadila Healthcare Limited | Process for the preparation of amorphous atorvastatin calcium |
| HU227041B1 (en) * | 2003-03-24 | 2010-05-28 | Richter Gedeon Nyrt | Process for the synthesis of amorphous atorvastatin calcium |
| 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 |
| US20050271717A1 (en) | 2003-06-12 | 2005-12-08 | Alfred Berchielli | Pharmaceutical compositions of atorvastatin |
| CZ298382B6 (cs) * | 2004-03-10 | 2007-09-12 | Zentiva, A. S. | Zpusob prípravy amorfní formy hemivápenaté soli atorvastatinu a její stabilizace |
| WO2005092852A1 (en) | 2004-03-17 | 2005-10-06 | Ranbaxy Laboratories Limited | Process for the production of atorvastatin calcium in amorphous form |
| CN1960972A (zh) * | 2004-04-16 | 2007-05-09 | 辉瑞产品公司 | 用于形成无定形阿托伐它汀钙的方法 |
| CN1692906A (zh) * | 2004-04-30 | 2005-11-09 | 鲁南制药集团股份有限公司 | 治疗高血脂症的组合物 |
| CA2649054A1 (en) | 2004-05-05 | 2005-11-10 | Pfizer Products Inc. | Salt forms of [r-(r*,r*)]-2-(4-fluorophenyl)-.beta., .delta.-dihydroxy-5-(1-methylethyl)-3-phenyl-4-[(phenylamino)carbonyl]-1h-pyrrole-1-heptanoic acid |
| CA2573969C (en) * | 2004-07-16 | 2014-02-04 | Lek Pharmaceuticals D.D. | Oxidative degradation products of atorvastatin calcium |
| JP2008506764A (ja) | 2004-07-20 | 2008-03-06 | ワーナー−ランバート カンパニー リミテッド ライアビリティー カンパニー | [R−(R*,R*)]−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−ヘプタン酸カルシウム塩(2:1)の新規形態 |
| WO2006037125A1 (en) | 2004-09-28 | 2006-04-06 | Teva Pharmaceutical Industries Ltd. | Process for preparing forms of atorvastatin calcium substantially free of impurities |
| CN101039906A (zh) * | 2004-10-18 | 2007-09-19 | 特瓦制药工业有限公司 | 通过将盐溶解于有机溶剂并除去该溶剂来制备无定形阿托伐他汀半钙的方法,所述有机溶剂为醇和酮和 /或酯的混合物 |
| WO2006046109A1 (en) | 2004-10-28 | 2006-05-04 | Warner-Lambert Company Llc | Process for forming amorphous atorvastatin |
| ATE466840T1 (de) | 2005-11-21 | 2010-05-15 | Warner Lambert Co | Neue formen von är-(r*,r*)ü-2-(4-fluorphenyl)-b,d-dihydroxy-5-( -methylethyl)-3-phenyl-4- ä(phenylamino)carbonylü-1h-pyrrol-1-heptansäure magnesium |
| EP1810667A1 (en) | 2006-01-20 | 2007-07-25 | KRKA, tovarna zdravil, d.d., Novo mesto | Pharmaceutical composition comprising amorphous atorvastatin |
| KR100833439B1 (ko) * | 2007-01-02 | 2008-05-29 | 씨제이제일제당 (주) | 비결정형 아토르바스타틴 칼슘의 개선된 제조방법 |
| 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 |
| HUP1000299A2 (hu) | 2010-06-08 | 2012-02-28 | Nanoform Cardiovascular Therapeutics Ltd | Nanostrukturált Atorvastatint, gyógyszerészetileg elfogadott sóit és kokristályait tartalmazó készítmény és eljárás elõállításukra |
| CN103274985B (zh) * | 2010-12-03 | 2016-03-09 | 上海科州药物研发有限公司 | 一种阿托伐他汀氨基酸盐 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| 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 |
| ATE123020T1 (de) * | 1990-05-11 | 1995-06-15 | American Cyanamid Co | N-acylierte arylpyrrole als insektizide, akarizide, nematizide und molluskizide wirkstoffe. |
| HRP960312B1 (en) * | 1995-07-17 | 2001-10-31 | Warner Lambert Co | NOVEL PROCESS FOR THE PRODUCTION OF AMORPHOUS /R-(R*, R*)/-2-(4-FLUOROPHENYL)-"beta", "delta"-DIHYDROXY-5-PHENYL-4-/(PHENYLAMINO)CARBONYL/-1H-PYRROLE -1-HEPTANOIC ACID CALCIUM SALT (2 : 1) |
| WO1998012200A1 (en) * | 1996-09-20 | 1998-03-26 | Meiji Seika Kaisha Ltd. | A crystalline substance of cefditoren pivoxyl and the production of the same |
-
1999
- 1999-10-18 HU HU9903634A patent/HU226640B1/hu not_active IP Right Cessation
-
2000
- 2000-10-17 KR KR1020027004906A patent/KR100664353B1/ko not_active Expired - Fee Related
- 2000-10-17 WO PCT/HU2000/000106 patent/WO2001028999A1/en not_active Ceased
- 2000-10-17 RU RU2002113564/04A patent/RU2255932C2/ru not_active IP Right Cessation
- 2000-10-17 CZ CZ20021256A patent/CZ300071B6/cs not_active IP Right Cessation
- 2000-10-17 PL PL00354604A patent/PL354604A1/xx not_active Application Discontinuation
- 2000-10-17 AU AU11663/01A patent/AU1166301A/en not_active Abandoned
- 2000-10-17 JP JP2001531799A patent/JP2003512354A/ja active Pending
- 2000-10-17 EP EP00973115A patent/EP1235800B1/en not_active Expired - Lifetime
- 2000-10-17 UA UA2002054059A patent/UA72777C2/uk unknown
- 2000-10-17 DE DE60031882T patent/DE60031882T2/de not_active Expired - Fee Related
- 2000-10-17 CN CNB008144583A patent/CN1157374C/zh not_active Expired - Fee Related
- 2000-10-17 HR HR20020334A patent/HRP20020334B1/xx not_active IP Right Cessation
- 2000-10-17 SK SK519-2002A patent/SK286861B6/sk not_active IP Right Cessation
- 2000-10-17 AT AT00973115T patent/ATE345327T1/de not_active IP Right Cessation
- 2000-10-17 CA CA002388018A patent/CA2388018C/en not_active Expired - Fee Related
- 2000-10-17 RS YUP-283/02A patent/RS50473B/sr unknown
Also Published As
| Publication number | Publication date |
|---|---|
| HUP9903634A3 (en) | 2002-01-28 |
| RU2255932C2 (ru) | 2005-07-10 |
| RS50473B (sr) | 2010-03-02 |
| HU226640B1 (en) | 2009-05-28 |
| YU28302A (sh) | 2005-06-10 |
| CA2388018C (en) | 2008-04-08 |
| ATE345327T1 (de) | 2006-12-15 |
| EP1235800A1 (en) | 2002-09-04 |
| CA2388018A1 (en) | 2001-04-26 |
| CN1379760A (zh) | 2002-11-13 |
| HUP9903634D0 (en) | 1999-12-28 |
| DE60031882T2 (de) | 2007-07-05 |
| SK5192002A3 (en) | 2002-11-06 |
| WO2001028999A1 (en) | 2001-04-26 |
| CN1157374C (zh) | 2004-07-14 |
| KR20020063166A (ko) | 2002-08-01 |
| AU1166301A (en) | 2001-04-30 |
| HUP9903634A2 (hu) | 2001-12-28 |
| DE60031882D1 (de) | 2006-12-28 |
| HK1050199A1 (en) | 2003-06-13 |
| HRP20020334A2 (en) | 2004-02-29 |
| HRP20020334B1 (hr) | 2007-12-31 |
| JP2003512354A (ja) | 2003-04-02 |
| SK286861B6 (sk) | 2009-06-05 |
| UA72777C2 (en) | 2005-04-15 |
| KR100664353B1 (ko) | 2007-01-02 |
| EP1235800B1 (en) | 2006-11-15 |
| CZ20021256A3 (cs) | 2002-08-14 |
| CZ300071B6 (cs) | 2009-01-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| YU28302A (sh) | Postupak za pripremanje amorfnog atorvastatin-kalcijuma | |
| Short et al. | A solid-phase combinatorial method for the synthesis of novel 5-and 6-membered ring lactams | |
| MY133511A (en) | Process for the production of amorphous atorvastatin calcium | |
| ATE243672T1 (de) | Neue thyroid-rezeptorliganden und verfahren | |
| Artamonov et al. | Synthesis of isomeric 6-trifluoromethyl-3-azabicyclo [3.1. 0] hexanes: Conformationally restricted analogues of 4-trifluoromethylpiperidine | |
| IL130338A0 (en) | Pyrroles as sPLA2 inhibitors | |
| JP2003512354A5 (cg-RX-API-DMAC7.html) | ||
| YU23499A (sh) | Inhibitorski amidi apo-b-sekrecije/mtp-a | |
| SE1102739T3 (cg-RX-API-DMAC7.html) | ||
| Liu et al. | A mild method for ring-opening aminolysis of lactones | |
| GR3025420T3 (en) | Process for solid support nucleic acid synthesis and compounds useful as solid supports in said process | |
| US6646133B1 (en) | Process for the preparation of amorphous atorvastatin calcium | |
| Barker et al. | A high yielding synthesis of anthranilate esters from sterically hindered alcohols | |
| Cerreti et al. | A novel synthesis of tricyclic-fused hydrindene–azetidinone compounds by sequential Mn (III)-promoted 4-exo-trig cyclization/radical aromatic substitution | |
| AU668161B2 (en) | Novel process and intermediates | |
| Vatèle | One-pot selective cleavage of prenyl carbamates using iodine in methanol followed by zinc | |
| Hoffmann et al. | Bioconversion of grindelic acid into 3α-hydroxygrindelic acid | |
| Delle Monache et al. | Iodolactonization of 3-amino-4-pentenoic acid: a stereoselective synthesis of syn-γ-hydroxy-β-amino acids | |
| LluisaáBennasar | A new synthetic entry to the alkaloids of the mavacurine group. First total synthesis of (▒)-2, 7-dihydropleiocarpamine | |
| US20040063969A1 (en) | Process for the preparation of amorphous atorvastatin calcium | |
| Pernfa | Stabilisation of a Cis Amide Bond in a Host-Guest Complex. Glen J. Pernfa, Jeremy D. Kilburn, Jonathan W. Essex, Russell J. Mortishire-Smith, and Michael Rowley | |
| Tantry et al. | Microwave accelerated efficient synthesis of N-fluorenylmethoxycarbonyl/t-butoxycarbonyl/benzyloxycarbonyl-5-oxazolidinones | |
| 김건철 et al. | An Efficient Transformation to the Structure of (±)-Supinidine | |
| IE85318B1 (en) | (R-(R*R*))-2-(4-fluorophenyl)-á,d-dihydroxy-5-(1-methylethyl-3-phenyl-4-[(phenylamino)carbonyl]-1H-pyrrole-1-heptanoic acid, its lactone form and salts thereof | |
| PL177187B1 (pl) | 2,3,4,3’,4’-penta -O-benzylo-sacharoza i sposób jej otrzymywania |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| REFS | Decisions on refusal to grant patents (taken after the publication of the particulars of the applications) |