ZA200106370B - Process for the production of tert-butyl (E)-(6[2- [-4(4-fluorophenyl) -6-isopropyl-2-[ methyl (methylsulfonyl) amino] pyrimidin-5-yl] vinyl](4R, 6S)-2,2-dimethyl [1,3]dioxan-4-yl)acetate. - Google Patents
Process for the production of tert-butyl (E)-(6[2- [-4(4-fluorophenyl) -6-isopropyl-2-[ methyl (methylsulfonyl) amino] pyrimidin-5-yl] vinyl](4R, 6S)-2,2-dimethyl [1,3]dioxan-4-yl)acetate.Info
- Publication number
- ZA200106370B ZA200106370B ZA200106370A ZA200106370A ZA200106370B ZA 200106370 B ZA200106370 B ZA 200106370B ZA 200106370 A ZA200106370 A ZA 200106370A ZA 200106370 A ZA200106370 A ZA 200106370A ZA 200106370 B ZA200106370 B ZA 200106370B
- Authority
- ZA
- South Africa
- Prior art keywords
- dioxan
- methylsulfonyl
- pyrimidin
- fluorophenyl
- tert
- Prior art date
Links
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 title 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 title 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 title 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 title 1
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 title 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 title 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 title 1
- 229920002554 vinyl polymer Polymers 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/645—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
- C07F9/6509—Six-membered rings
- C07F9/6512—Six-membered rings having the nitrogen atoms in positions 1 and 3
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Heart & Thoracic Surgery (AREA)
- Molecular Biology (AREA)
- Biochemistry (AREA)
- Cardiology (AREA)
- Obesity (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB9903472.0A GB9903472D0 (en) | 1999-02-17 | 1999-02-17 | Chemical process |
Publications (1)
Publication Number | Publication Date |
---|---|
ZA200106370B true ZA200106370B (en) | 2002-11-04 |
Family
ID=10847843
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ZA200106370A ZA200106370B (en) | 1999-02-17 | 2001-08-02 | Process for the production of tert-butyl (E)-(6[2- [-4(4-fluorophenyl) -6-isopropyl-2-[ methyl (methylsulfonyl) amino] pyrimidin-5-yl] vinyl](4R, 6S)-2,2-dimethyl [1,3]dioxan-4-yl)acetate. |
Country Status (34)
Country | Link |
---|---|
US (2) | US6844437B1 (fr) |
EP (1) | EP1155015B1 (fr) |
JP (3) | JP2003518474A (fr) |
KR (1) | KR100648160B1 (fr) |
CN (1) | CN1145625C (fr) |
AR (1) | AR022600A1 (fr) |
AT (1) | ATE415398T1 (fr) |
AU (1) | AU760145B2 (fr) |
BR (1) | BRPI0008301B8 (fr) |
CA (1) | CA2362594C (fr) |
CL (1) | CL2003002336A1 (fr) |
CY (1) | CY1108733T1 (fr) |
CZ (1) | CZ299844B6 (fr) |
DE (1) | DE60040905D1 (fr) |
DK (1) | DK1155015T3 (fr) |
EE (2) | EE05531B1 (fr) |
ES (1) | ES2316349T3 (fr) |
GB (1) | GB9903472D0 (fr) |
HK (1) | HK1041265B (fr) |
HU (1) | HU229835B1 (fr) |
IL (2) | IL144793A0 (fr) |
IS (1) | IS2711B (fr) |
MX (1) | MXPA01008235A (fr) |
NO (1) | NO320739B1 (fr) |
NZ (1) | NZ513261A (fr) |
PL (1) | PL218518B1 (fr) |
PT (1) | PT1155015E (fr) |
RU (1) | RU2243969C2 (fr) |
SI (1) | SI1155015T1 (fr) |
SK (1) | SK286988B6 (fr) |
TR (2) | TR200401874T2 (fr) |
TW (1) | TWI285202B (fr) |
WO (1) | WO2000049014A1 (fr) |
ZA (1) | ZA200106370B (fr) |
Families Citing this family (83)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE9902202D0 (sv) * | 1999-06-10 | 1999-06-10 | Astra Ab | Production of aggregates |
GB0003305D0 (en) * | 2000-02-15 | 2000-04-05 | Zeneca Ltd | Pyrimidine derivatives |
GB0011120D0 (en) * | 2000-05-09 | 2000-06-28 | Avecia Ltd | Process |
NL1015744C2 (nl) * | 2000-07-19 | 2002-01-22 | Dsm Nv | Werkwijze voor de bereiding van 2-(6-gesubstitueerde-1,3-dioxan-4-yl) azijnzuurderivaten. |
AU2002318041B2 (en) | 2001-07-13 | 2008-01-03 | Astrazeneca Uk Limited | Preparation of aminopyrimidine compounds |
MXPA04001451A (es) * | 2001-08-16 | 2005-02-17 | Teva Pharma | Procesos para preparar formas de sal de calcio de estatinas. |
EP1323717A1 (fr) * | 2001-12-27 | 2003-07-02 | Dsm N.V. | Procédé de Préparation de Dérivés de l'acide 2-(1,3-dioxane-4-yl substitué en 6) acétique |
EP1375493A1 (fr) * | 2002-06-17 | 2004-01-02 | Dsm N.V. | Procédé de fabrication d'un ester d'acide acétique de dioxane |
GB0218781D0 (en) * | 2002-08-13 | 2002-09-18 | Astrazeneca Ab | Chemical process |
EP1578731B1 (fr) * | 2002-12-16 | 2009-11-11 | AstraZeneca UK Limited | Composes et procedes |
GB0312896D0 (en) * | 2003-06-05 | 2003-07-09 | Astrazeneca Ab | Chemical process |
WO2005023778A2 (fr) | 2003-08-28 | 2005-03-17 | Teva Pharmaceutical Industries Ltd. | Procede de preparation de sels calciques de rosuvastatine |
UY28501A1 (es) * | 2003-09-10 | 2005-04-29 | Astrazeneca Uk Ltd | Compuestos químicos |
GB0321827D0 (en) * | 2003-09-18 | 2003-10-15 | Astrazeneca Uk Ltd | Chemical compounds |
GB0322552D0 (en) | 2003-09-26 | 2003-10-29 | Astrazeneca Uk Ltd | Therapeutic treatment |
GB0324791D0 (en) * | 2003-10-24 | 2003-11-26 | Astrazeneca Ab | Chemical process |
CA2546701C (fr) * | 2003-11-24 | 2010-07-27 | Teva Pharmaceutical Industries Ltd. | Sels d'ammonium cristallins de la rosuvastatine |
CN1894221B (zh) | 2003-12-02 | 2012-08-08 | 特瓦制药工业有限公司 | 用于表征罗苏伐他汀的参照标准品 |
US7241800B2 (en) | 2004-03-17 | 2007-07-10 | Mai De Ltd. | Anhydrous amorphous form of fluvastatin sodium |
GB0406757D0 (en) | 2004-03-26 | 2004-04-28 | Avecia Ltd | Process and compounds |
WO2006017357A1 (fr) | 2004-07-13 | 2006-02-16 | Teva Pharmaceutical Industries Ltd. | Procede pour la preparation de rosuvastatine mettant en oeuvre une etape d'oxydation par tempo |
GB0427491D0 (en) | 2004-12-16 | 2005-01-19 | Avecia Ltd | Process and compounds |
GB0428328D0 (en) * | 2004-12-24 | 2005-02-02 | Astrazeneca Uk Ltd | Chemical process |
CN100351240C (zh) * | 2005-01-19 | 2007-11-28 | 安徽省庆云医药化工有限公司 | 瑞舒伐他汀钙的合成方法 |
WO2006091771A2 (fr) | 2005-02-22 | 2006-08-31 | Teva Pharmaceutical Industries Ltd. | Elaboration de la rosuvastatine |
EP1863773A1 (fr) * | 2005-03-22 | 2007-12-12 | Unichem Laboratories Limited | Procede de preparation de la rosuvastatine |
US20080161560A1 (en) * | 2005-04-04 | 2008-07-03 | Pandurang Balwant Deshpande | Process for Preparation of Calcium Salt of Rosuvastatin |
HU227120B1 (hu) * | 2005-05-26 | 2010-07-28 | Richter Gedeon Nyrt | Eljárás rosuvastatin kalciumsójának elõállítására új intermediereken keresztül |
AU2006261087B2 (en) * | 2005-06-24 | 2010-09-30 | Lek Pharmaceuticals D.D. | Process for preparing amorphous rosuvastatin calcium free of impurities |
WO2006136408A2 (fr) * | 2005-06-24 | 2006-12-28 | Lek Pharmaceuticals D.D. | Procédé de préparation de rosuvastatine calcique pure amorphe |
GB0514078D0 (en) * | 2005-07-08 | 2005-08-17 | Astrazeneca Uk Ltd | Chemical process |
WO2007017117A1 (fr) * | 2005-07-28 | 2007-02-15 | Lek Pharmaceuticals D.D. | Processus destine a la synthese de calcium rosuvastatine |
BRPI0605917A2 (pt) | 2005-08-16 | 2009-05-26 | Teva Pharma | intermediário cristalino de rosuvastatina |
CN100436428C (zh) * | 2005-08-22 | 2008-11-26 | 鲁南制药集团股份有限公司 | 瑞舒伐他汀及其盐的制备方法 |
CN100352821C (zh) * | 2005-08-22 | 2007-12-05 | 鲁南制药集团股份有限公司 | 一种瑞舒伐他汀钙中间体的制备方法 |
ES2564250T3 (es) * | 2006-05-03 | 2016-03-21 | Msn Laboratories Private Limited | Nuevo proceso para estatinas y sus sales farmacéuticamente aceptables de las mismas |
EP2086945B1 (fr) | 2006-10-09 | 2016-01-06 | MSN Laboratories Private Limited | Nouveau procédé de préparation de statines et leurs sels pharmaceutiquement acceptables |
EP2079712A2 (fr) | 2006-10-31 | 2009-07-22 | Aurobindo Pharma Limited | Procédé amélioré de préparation de rosuvastatine calcique |
TW200831469A (en) * | 2006-12-01 | 2008-08-01 | Astrazeneca Uk Ltd | Chemical process |
WO2008072078A1 (fr) | 2006-12-13 | 2008-06-19 | Aurobindo Pharma Limited | Procédé amélioré de préparation de calcium de rosuvastatine |
CA2677809A1 (fr) | 2007-02-08 | 2008-08-14 | Aurobindo Pharma Limited | Procede perfectionne pour la preparation de rosuvastatine calcique |
KR20090018964A (ko) | 2007-04-18 | 2009-02-24 | 테바 파마슈티컬 인더스트리즈 리미티드 | Hmg-coa 환원 효소 억제제의 중간체의 제조 방법 |
US7884226B2 (en) | 2007-07-12 | 2011-02-08 | Teva Pharmaceutical Industries, Ltd. | Purification of rosuvatatin intermediate by thin film evaporation and chemical method |
US20110065920A1 (en) | 2007-08-28 | 2011-03-17 | Ratiopharm Gmbh | Process for preparing pentanoic diacid derivatives |
CN101376647B (zh) * | 2007-08-31 | 2010-12-08 | 中山奕安泰医药科技有限公司 | 一种用于合成瑞舒伐他汀中间体及瑞舒伐他汀的合成方法 |
CA2725052C (fr) | 2008-05-27 | 2014-09-16 | Changzhou Pharmaceutical Factory Co., Ltd. | Procede de preparation de la rosuvastatine calcique et de ses intermediaires |
EP2138165A1 (fr) | 2008-06-27 | 2009-12-30 | KRKA, tovarna zdravil, d.d., Novo mesto | Composition pharmaceutique comportant de la statine |
ES2657416T3 (es) | 2008-06-27 | 2018-03-05 | Krka, Torvarna Zdravil, D.D., Novo Mesto | Composición farmacéutica que comprende una estatina |
RU2011112541A (ru) * | 2008-09-09 | 2012-10-20 | Биокон Лимитед (In) | Способ получения кальциевой соли (3r,5s,6e)6-{2-[4-(4фторфенил)-6-изопропил-2-(метансульфонилметиламино)-пиримидин-5-ил]-винил}-2,2-диметил-[1,3]-диоксан-4-ил)-уксусной кислоты(ацетонид розувастатина кальция) |
US8394956B2 (en) * | 2008-09-30 | 2013-03-12 | Aurobindo Pharma Ltd. | Process for preparing pyrimidine propenaldehyde |
EP2351762B1 (fr) * | 2008-10-20 | 2013-10-16 | Kaneka Corporation | NOUVEAU DÉRIVÉ DE PYRIMIDINE ET MÉTHODE DE PRODUCTION D'UN INTERMÉDIAIRE D'INHIBITEUR DE HMG-CoA RÉDUCTASE |
EP2373609B1 (fr) | 2008-12-19 | 2013-10-16 | KRKA, D.D., Novo Mesto | Utilisation de composés amphiphiles pour la cristallisation régulée de statines et d'intermédiaires de statines |
EP2327682A1 (fr) | 2009-10-29 | 2011-06-01 | KRKA, D.D., Novo Mesto | Utilisation de composés amphiphiles pour la crystallisation controlée de statines et d'intermediaires de statines. |
WO2010077062A2 (fr) * | 2008-12-29 | 2010-07-08 | Hanmi Pharm. Co., Ltd. | Méthode de synthèse d'une statine et benzothiazolylsulfone y étant employée |
WO2010081861A1 (fr) | 2009-01-14 | 2010-07-22 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Procédé de préparation de rosuvastatine |
US8487105B2 (en) | 2009-01-19 | 2013-07-16 | Msn Laboratories Limited | Process for preparing pitavastatin, intermediates and pharmaceuctically acceptable salts thereof |
KR101157314B1 (ko) | 2009-06-05 | 2012-06-15 | 주식회사종근당 | 로수바스타틴의 신규한 제조방법, 이 제조에 유용한 중간체 화합물 및 그의 제조방법 |
WO2011086584A2 (fr) | 2010-01-18 | 2011-07-21 | Msn Laboratories Limited | Procédé amélioré pour la préparation d'intermédiaires amides et leur utilisation |
WO2011104725A2 (fr) | 2010-02-23 | 2011-09-01 | Cadila Healthcare Limited | Inhibiteurs de l'hmg-coa réductase et procédé pour leur préparation |
WO2012011129A2 (fr) * | 2010-07-22 | 2012-01-26 | Msn Laboratories Limited | Nouveau polymorphe de sel de calcium d'acide bis[(e)-7-[4-(4-fluorophényl)-6-iso-propyl-2-[méthyl (méthylsulfonyl)amino]pyrimidin-5-yl](3r,5s)-3,5-dihydroxyhept-6-énoïque] |
WO2012073256A1 (fr) | 2010-11-29 | 2012-06-07 | Cadila Healthcare Limited | Sels de rosuvastatine |
SI2665721T1 (sl) | 2011-01-18 | 2015-10-30 | Dsm Sinochem Pharmaceuticals Netherlands B.V. | Metiltetrazol sulfidi in sulfoni |
HUE025730T2 (en) | 2011-01-18 | 2016-04-28 | Dsm Sinochem Pharm Nl Bv | A method for producing statins using a base |
SI2665722T1 (sl) | 2011-01-18 | 2016-12-30 | Dsm Sinochem Pharmaceuticals Netherlands B.V. | Postopek priprave diol sulfonov |
WO2012172564A1 (fr) * | 2011-05-25 | 2012-12-20 | Dr. Reddy's Laboratories Limited | Procédé de préparation de calcium de rosuvastatine |
MX363563B (es) | 2011-12-09 | 2019-03-27 | Dsm Sinochem Pharm Nl Bv | Proceso para la preparación de un tioprecursor de estatinas. |
CN103974946B (zh) | 2011-12-09 | 2017-09-29 | 中化帝斯曼制药有限公司荷兰公司 | 制备他汀前体的方法 |
KR20130087153A (ko) * | 2012-01-27 | 2013-08-06 | 코오롱생명과학 주식회사 | 로수바스타틴의 제조방법 및 이에 사용되는 중간체 화합물 |
CN103232398B (zh) * | 2012-04-28 | 2016-04-06 | 上海科州药物研发有限公司 | 一种瑞舒伐他汀氨基酸盐及其制备方法和应用 |
KR101292743B1 (ko) * | 2012-05-17 | 2013-08-02 | (주) 에프엔지리서치 | 신규한 스타틴 중간체 및 이를 이용한 피타바스타틴, 로수바스타틴, 세리바스타틴 및 플루바스타틴의 제조 방법 |
CN103864697A (zh) * | 2012-12-11 | 2014-06-18 | 润泽制药(苏州)有限公司 | 瑞舒伐中间体主链醇的制备方法 |
WO2014108795A2 (fr) | 2013-01-10 | 2014-07-17 | Aurobindo Pharma Limited | Procédé de préparation amélioré de diol sulfones chirales et de statines |
CN103420919B (zh) * | 2013-08-22 | 2015-07-08 | 南京欧信医药技术有限公司 | 一种嘧啶类衍生物的合成方法 |
WO2015037018A1 (fr) * | 2013-09-14 | 2015-03-19 | Ind-Swift Laboratories Limited | Procédé de préparation de rosuvastatine par le biais de nouveaux intermédiaires |
PT3115367T (pt) * | 2014-03-07 | 2018-01-04 | Asymchem Laboratories Fuxin Co Ltd | Composto intermediário para preparar rosuvastatina cálcica e método para preparar rosuvastatina cálcica a partir deste |
CN103936680B (zh) * | 2014-04-18 | 2016-08-24 | 润泽制药(苏州)有限公司 | 瑞舒伐他汀钙已知杂质的制备方法 |
CN104788387A (zh) * | 2015-04-17 | 2015-07-22 | 浙江海森药业有限公司 | 高纯度瑞舒伐他汀钙的制备方法 |
KR20160126700A (ko) | 2015-04-24 | 2016-11-02 | 미래파인켐 주식회사 | 스타틴의 중간체, 이의 제조방법 및 이를 이용한 로수바스타틴의 제조방법 |
CN105461636A (zh) * | 2015-12-30 | 2016-04-06 | 安徽美诺华药物化学有限公司 | 一种瑞舒伐他汀甲酯的合成方法 |
CN106478518A (zh) * | 2016-09-27 | 2017-03-08 | 南通常佑药业科技有限公司 | 一种庚烯酸环戊酯衍生物的制备方法 |
KR101953575B1 (ko) | 2016-10-24 | 2019-05-24 | 한양대학교 에리카산학협력단 | 스타틴계 고지혈증 치료제 합성을 위한 새로운 중간체 합성 및 이를 이용한 로수바스타틴 합성 공정 개발 |
CN108997324A (zh) * | 2018-08-21 | 2018-12-14 | 南京欧信医药技术有限公司 | 瑞舒伐他汀钙中间体的制备方法 |
CN109651259B (zh) * | 2018-12-29 | 2020-05-19 | 浙江永太科技股份有限公司 | 一种瑞舒伐他汀钙关键中间体的纯化方法 |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3741509A1 (de) * | 1987-12-08 | 1989-06-22 | Hoechst Ag | Verfahren zur herstellung optisch aktiver 3-desmethylmevalonsaeurederivate sowie zwischenprodukte |
JP2648897B2 (ja) | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
FR2741620B1 (fr) * | 1995-11-28 | 1997-12-26 | Oreal | Procede de preparation de composes a groupement beta-hydroxy -delta-lactone analogues de la (+) compactine et de la (+) mevinoline |
-
1999
- 1999-02-17 GB GBGB9903472.0A patent/GB9903472D0/en not_active Ceased
-
2000
- 2000-02-15 DE DE60040905T patent/DE60040905D1/de not_active Expired - Lifetime
- 2000-02-15 TR TR2004/01874T patent/TR200401874T2/xx unknown
- 2000-02-15 EE EEP200900043A patent/EE05531B1/xx unknown
- 2000-02-15 EP EP00903810A patent/EP1155015B1/fr not_active Expired - Lifetime
- 2000-02-15 HU HU0200301A patent/HU229835B1/hu unknown
- 2000-02-15 WO PCT/GB2000/000481 patent/WO2000049014A1/fr active IP Right Grant
- 2000-02-15 PT PT00903810T patent/PT1155015E/pt unknown
- 2000-02-15 IL IL14479300A patent/IL144793A0/xx not_active IP Right Cessation
- 2000-02-15 JP JP2000599753A patent/JP2003518474A/ja not_active Withdrawn
- 2000-02-15 AR ARP000100642A patent/AR022600A1/es active IP Right Grant
- 2000-02-15 CA CA002362594A patent/CA2362594C/fr not_active Expired - Fee Related
- 2000-02-15 AU AU25573/00A patent/AU760145B2/en not_active Expired
- 2000-02-15 CZ CZ20012930A patent/CZ299844B6/cs not_active IP Right Cessation
- 2000-02-15 MX MXPA01008235A patent/MXPA01008235A/es active IP Right Grant
- 2000-02-15 US US09/913,539 patent/US6844437B1/en not_active Expired - Lifetime
- 2000-02-15 ES ES00903810T patent/ES2316349T3/es not_active Expired - Lifetime
- 2000-02-15 TR TR2001/02360T patent/TR200102360T2/xx unknown
- 2000-02-15 NZ NZ513261A patent/NZ513261A/en not_active IP Right Cessation
- 2000-02-15 AT AT00903810T patent/ATE415398T1/de active
- 2000-02-15 KR KR1020017010439A patent/KR100648160B1/ko active IP Right Grant
- 2000-02-15 PL PL350185A patent/PL218518B1/pl unknown
- 2000-02-15 RU RU2001125421/04A patent/RU2243969C2/ru active
- 2000-02-15 EE EEP200100430A patent/EE05150B1/xx unknown
- 2000-02-15 BR BRPI0008301A patent/BRPI0008301B8/pt not_active IP Right Cessation
- 2000-02-15 CN CNB008037043A patent/CN1145625C/zh not_active Expired - Lifetime
- 2000-02-15 SK SK1183-2001A patent/SK286988B6/sk not_active IP Right Cessation
- 2000-02-15 SI SI200031016T patent/SI1155015T1/sl unknown
- 2000-02-15 DK DK00903810T patent/DK1155015T3/da active
- 2000-03-10 TW TW089104365A patent/TWI285202B/zh not_active IP Right Cessation
-
2001
- 2001-07-31 IS IS6029A patent/IS2711B/is unknown
- 2001-08-02 ZA ZA200106370A patent/ZA200106370B/xx unknown
- 2001-08-16 NO NO20013994A patent/NO320739B1/no not_active IP Right Cessation
-
2002
- 2002-04-22 HK HK02103022.4A patent/HK1041265B/zh not_active IP Right Cessation
-
2003
- 2003-07-02 US US10/610,700 patent/US6784171B2/en not_active Expired - Lifetime
- 2003-11-12 CL CL200302336A patent/CL2003002336A1/es unknown
-
2004
- 2004-08-05 IL IL163375A patent/IL163375A/en not_active IP Right Cessation
-
2007
- 2007-05-08 JP JP2007123108A patent/JP4130844B2/ja not_active Expired - Lifetime
-
2008
- 2008-03-17 JP JP2008067100A patent/JP2008255114A/ja active Pending
-
2009
- 2009-01-29 CY CY20091100107T patent/CY1108733T1/el unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ZA200106370B (en) | Process for the production of tert-butyl (E)-(6[2- [-4(4-fluorophenyl) -6-isopropyl-2-[ methyl (methylsulfonyl) amino] pyrimidin-5-yl] vinyl](4R, 6S)-2,2-dimethyl [1,3]dioxan-4-yl)acetate. | |
HUP9801587A3 (en) | 5h-thiazolo[3,2-a]pyrimidine derivatives, process for their preparation, intermediates, use of the compounds and pharmaceutical compositions containing them | |
AU9392598A (en) | Substituted 3(-1,2-benzisothiazol or isoxazol-5 yl)-substituted pyrimidine as herbicides | |
AU2759800A (en) | Processes and intermediates for the preparation of 1,3-oxazin-6-ones and uracils | |
HUP0303590A3 (en) | Method for the production of 4,6-diaminopyrimido[5,4-d]pyrimidines | |
AU3420099A (en) | Process for the production of purine derivatives and intermediates therefor | |
AU2159797A (en) | Substituted pyridines/pyrimidines, process for the preparation thereof and use thereof as pesticides | |
ZA200108392B (en) | Process for the preparation of substituted pyrimidines. | |
AU2003235951A1 (en) | Process for the preparation of 2-aminopyrazine derivatives | |
AU2002359160A1 (en) | PIPAZOLO (1,5-a) PYRIMIDINE DERIVATIVES AS MODULATORS OF PPAR | |
EG22775A (en) | Process for the preparation of pyrazolo (f,5-d) pyrimidin 7 ones-3-pyridylsulphonyl compounds and intermediates thereof | |
AU6870600A (en) | Process for the preparation of 2,3-dihydroazepine compounds | |
AU2992800A (en) | Process for the preparation of 6-(perfluoroalkyl)uracil compounds | |
AU6434900A (en) | Method for the production of 4,6-dichloropyrimidine with the aid of phosgene | |
CZ20012431A3 (cs) | Způsob výroby (4R,6R)tert-butyl[6-(2-aminoethyl)-2,2-dimethyl[1,3]dioxan-4-yl]acetatu a meziproduktů pro jeho výrobu | |
IL121031A0 (en) | Process for the preparation of 5-(alkoxymethyl)-2,3-pyridinedicarboximide compounds | |
AU3231500A (en) | Process for the preparation of 6-(perfluoroalkyl) uracil compounds from urea compounds | |
AU1079100A (en) | 2-(substituted phenylimino)pyrimidine derivatives, intermediates in the production thereof, process for producing the same and pesticides containing the same asthe active ingredient | |
AU5514199A (en) | Process for the preparation of 2-(aryloxymethyl)-2,5,7,8-tetramethylchroman-6-ols | |
DE69630561D1 (de) | Verwendung von 4-Amino-6-hydroxypyrazolo[3,4-d]pyrimidin zur Herstellung eines blutdrucksenkenden Mittels | |
AU2001262240A1 (en) | Process for the production of 2,2,6-trimethylcyclohexane-1,4-dione | |
AU5197899A (en) | Indole compounds, process for the preparation of the same and uses thereof | |
AU1657900A (en) | Process for the preparation of pyrimidinone derivatives | |
AU2002234623A1 (en) | Process for the preparation of 3,5,5-trimethyl-cyclohex-2-ene-1,4-dione | |
SI1200414T1 (en) | Process for the preparation of substituted pyrimidines |