ES2110499T3 - Intermediario opticamente activo y su produccion. - Google Patents
Intermediario opticamente activo y su produccion.Info
- Publication number
- ES2110499T3 ES2110499T3 ES92910210T ES92910210T ES2110499T3 ES 2110499 T3 ES2110499 T3 ES 2110499T3 ES 92910210 T ES92910210 T ES 92910210T ES 92910210 T ES92910210 T ES 92910210T ES 2110499 T3 ES2110499 T3 ES 2110499T3
- Authority
- ES
- Spain
- Prior art keywords
- optically active
- production
- represents hydrogen
- active intermediary
- cn2s
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 102000004286 Hydroxymethylglutaryl CoA Reductases Human genes 0.000 abstract 1
- 108090000895 Hydroxymethylglutaryl CoA Reductases Proteins 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 235000012000 cholesterol Nutrition 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 230000002401 inhibitory effect Effects 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 230000002194 synthesizing effect Effects 0.000 abstract 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/535—Organo-phosphoranes
- C07F9/5352—Phosphoranes containing the structure P=C-
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C315/00—Preparation of sulfones; Preparation of sulfoxides
- C07C315/04—Preparation of sulfones; Preparation of sulfoxides by reactions not involving the formation of sulfone or sulfoxide groups
-
- 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
- C07D207/46—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with hetero atoms directly attached to the ring nitrogen atom
- C07D207/48—Sulfur 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
-
- 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
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
- C07F7/1804—Compounds having Si-O-C linkages
- C07F7/1872—Preparation; Treatments not provided for in C07F7/20
- C07F7/1892—Preparation; Treatments not provided for in C07F7/20 by reactions not provided for in C07F7/1876 - C07F7/1888
-
- 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
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4003—Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4006—Esters of acyclic acids which can have further substituents on alkyl
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Steroid Compounds (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Pyrrole Compounds (AREA)
Abstract
SE DESCRIBE UN PROCESO PARA SINTETIZAR UN MATERIAL DE PARTIDA ACTIVO OPTICAMENTE, REPRESENTADO POR LA FORMULA GENERAL (I), PARA DIFERENTES MEDICINAS CON UNA ELEVADA PUREZA OPTICA CON BUEN RENDIMIENTO, EN LA QUE R1 REPRESENTA HIDROGENO O GRUPO PROTECTOR HIDROXILO: * REPRESENTA UN ATOMO DE CARBON ASIMETRICO; R2 REPRESENTA HIDROGENO O ALQUILO MAS BAJO SUSTITUIDO OPCIONALMENTE; Y Q REPRESENTA -C = P(PH)3, -CH2P(P)(OME)2 O -CN2S(O)ME. MAS PARTICULARMENTE, UN PRODUCTO INTERMEDIO PARA LA SINTESIS DE UN COMPUESTO ACTIVO OPTICAMENTE UTIL PAA INHIBIR LA ACTIVIDAD DE LA REDUCTASA HMG-COA PARA INHIBIR POR ELLO LA BIOSINTESIS DE COLESTEROL; Y UN PROCESO PARA PRODUCIR EL PRODUCTO INTERMEDIO.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17620991 | 1991-06-19 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2110499T3 true ES2110499T3 (es) | 1998-02-16 |
Family
ID=16009533
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES92910210T Expired - Lifetime ES2110499T3 (es) | 1991-06-19 | 1992-05-14 | Intermediario opticamente activo y su produccion. |
Country Status (11)
Country | Link |
---|---|
US (1) | US5354879A (es) |
EP (1) | EP0554455B1 (es) |
JP (2) | JP3233403B2 (es) |
KR (1) | KR100216011B1 (es) |
AT (1) | ATE161262T1 (es) |
DE (1) | DE69223603T2 (es) |
DK (1) | DK0554455T3 (es) |
ES (1) | ES2110499T3 (es) |
GR (1) | GR3026204T3 (es) |
TW (1) | TW201730B (es) |
WO (1) | WO1992022560A1 (es) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5717124A (en) * | 1993-03-30 | 1998-02-10 | Ube Industries, Ltd. | Process for preparation of oxyglutaric acid ester derivatives |
DE69424463T2 (de) * | 1993-03-30 | 2000-09-14 | Ube Industries, Ltd. | Verfahren zur Herstellung von Ester-Derivaten der Oxyglutar-Säure |
US6376476B1 (en) * | 1996-12-13 | 2002-04-23 | Zymogenetics Corporation | Isoprenoid pathway inhibitors for stimulating bone growth |
US6121475A (en) * | 1999-09-17 | 2000-09-19 | Ube Industries, Ltd. | Preparation of optically active β-hydroxyester derivatives and platinum-containing catalyst |
KR100511533B1 (ko) * | 2002-04-09 | 2005-08-31 | 임광민 | 키랄 중간체, 그의 제조방법 및 그를 이용한 HMG-CoA환원저해제의 제조방법 |
GB0211751D0 (en) * | 2002-05-22 | 2002-07-03 | Avecia Ltd | Compound and process |
CA2657076A1 (en) * | 2003-08-28 | 2005-03-17 | Teva Pharmaceutical Industries Ltd. | Process for the preparation of rosuvastatin calcium |
US7777034B2 (en) * | 2003-11-24 | 2010-08-17 | Teva Pharmaceutical Industries Ltd. | Crystalline ammonium salts of rosuvastatin |
ES2364143T3 (es) * | 2003-12-02 | 2011-08-25 | Teva Pharmaceutical Industries Ltd. | Estandar de referencia para caracterización de rosuvastatina. |
US7851624B2 (en) | 2003-12-24 | 2010-12-14 | Teva Pharamaceutical Industries Ltd. | Triol form of rosuvastatin and synthesis of rosuvastatin |
CA2573857A1 (en) * | 2004-07-13 | 2006-02-16 | Teva Pharmaceutical Industries Ltd. | A process for the preparation of rosuvastatin involving a tempo-mediated oxidation step |
TWI345562B (en) | 2005-02-22 | 2011-07-21 | Teva Pharma | Rosuvastatin and salts thereof free of rosuvastatin alkylether and a process for the preparation thereof |
US20070037979A1 (en) * | 2005-02-22 | 2007-02-15 | Valerie Niddam-Hildesheim | Preparation of rosuvastatin |
US20070167625A1 (en) * | 2005-02-22 | 2007-07-19 | Anna Balanov | Preparation of rosuvastatin |
MX2007004427A (es) * | 2005-08-16 | 2007-06-14 | Teva Pharma | Intermedio de rosuvastatina cristalina. |
CN1958593B (zh) * | 2005-11-03 | 2010-05-05 | 上海医药工业研究院 | 一种用于合成瑞舒伐他汀钙的中间体的制备方法 |
JP2009531466A (ja) | 2007-04-18 | 2009-09-03 | テバ ファーマシューティカル インダストリーズ リミティド | HMG−CoA還元酵素阻害剤の中間体の製造方法 |
EP2178890A1 (en) * | 2007-07-12 | 2010-04-28 | Teva Pharmaceutical Industries Ltd. | Purification of rosuvastatin intermediate by thin film evaporation and chemical method |
EA201000214A1 (ru) | 2007-08-28 | 2010-10-29 | Рациофарм Гмбх | Способ получения производных пентадикарбоновой кислоты |
CN101735272B (zh) * | 2009-12-11 | 2012-10-31 | 重庆博腾制药科技股份有限公司 | 瑞舒伐他汀钙中间体的制备方法 |
EP2785851A2 (en) * | 2011-11-28 | 2014-10-08 | Mylan Laboratories, Limited | Process for producing chiral statin side chain intermediates employing candida antarctica lipase b |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1421555A (en) * | 1972-03-17 | 1976-01-21 | Searle & Co | Process for the stereoselective production of intermediates in the synthesis of pge1 and derivatives |
US3907852A (en) * | 1972-06-23 | 1975-09-23 | Exxon Research Engineering Co | Silylhydrocarbyl phosphines and related compounds |
DE3722807A1 (de) * | 1987-07-10 | 1989-01-19 | Hoechst Ag | Neue 3,5-dihydroxycarbonsaeuren und deren derivate, verfahren zu ihrer herstellung, ihre verwendung als arzneimittel, pharmazeutische praeparate und zwischenprodukte |
WO1989003212A1 (en) * | 1987-10-13 | 1989-04-20 | Pfizer Inc. | 3,5-dihydroxy-6,8-nonadienoic acids and derivatives as hypocholesterolemic agents |
US4804770A (en) * | 1988-04-29 | 1989-02-14 | E. R. Squibb & Sons, Inc. | Process for preparing a keto-phosphonate intermediate useful in preparing HMG-CoA reductase inhibitors |
DE3832570A1 (de) * | 1988-09-24 | 1990-03-29 | Hoechst Ag | 7-substituierte derivate der 3,5-dihydroxyhept-6-insaeure, verfahren zur ihrer herstellung, ihre verwendung als arzneimittel, sowie zwischenprodukte |
US5117039A (en) * | 1988-12-14 | 1992-05-26 | Shionogi & Co., Ltd. | Monoesters of arylacetic acid and the process thereof |
JP2719723B2 (ja) * | 1988-12-14 | 1998-02-25 | 塩野義製薬株式会社 | アリール酢酸モノエステル類およびその製造法 |
US5093363A (en) * | 1989-08-22 | 1992-03-03 | Shionogi & Co., Ltd. | 2,4,6-substituted phenol derivatives |
-
1992
- 1992-05-14 DK DK92910210.1T patent/DK0554455T3/da active
- 1992-05-14 ES ES92910210T patent/ES2110499T3/es not_active Expired - Lifetime
- 1992-05-14 JP JP50928592A patent/JP3233403B2/ja not_active Expired - Lifetime
- 1992-05-14 US US07/969,249 patent/US5354879A/en not_active Expired - Lifetime
- 1992-05-14 AT AT92910210T patent/ATE161262T1/de active
- 1992-05-14 WO PCT/JP1992/000611 patent/WO1992022560A1/ja active IP Right Grant
- 1992-05-14 DE DE69223603T patent/DE69223603T2/de not_active Expired - Lifetime
- 1992-05-14 EP EP92910210A patent/EP0554455B1/en not_active Expired - Lifetime
- 1992-06-11 TW TW081104572A patent/TW201730B/zh active
-
1993
- 1993-02-18 KR KR1019930700459A patent/KR100216011B1/ko not_active IP Right Cessation
-
1998
- 1998-02-25 GR GR980400381T patent/GR3026204T3/el unknown
-
2001
- 2001-07-18 JP JP2001218860A patent/JP3635247B2/ja not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
JP3635247B2 (ja) | 2005-04-06 |
JP2002088054A (ja) | 2002-03-27 |
ATE161262T1 (de) | 1998-01-15 |
GR3026204T3 (en) | 1998-05-29 |
DK0554455T3 (da) | 1998-01-19 |
EP0554455A4 (es) | 1994-03-23 |
EP0554455A1 (en) | 1993-08-11 |
JP3233403B2 (ja) | 2001-11-26 |
KR930701460A (ko) | 1993-06-11 |
US5354879A (en) | 1994-10-11 |
TW201730B (es) | 1993-03-11 |
EP0554455B1 (en) | 1997-12-17 |
DE69223603T2 (de) | 1998-04-09 |
WO1992022560A1 (en) | 1992-12-23 |
DE69223603D1 (de) | 1998-01-29 |
KR100216011B1 (ko) | 1999-08-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ES2110499T3 (es) | Intermediario opticamente activo y su produccion. | |
AU4497993A (en) | Novel processes for the production of 13-ether derivatives of milbemycins, and novel intermediates therefor | |
NO991019D0 (no) | 3-merkapto-1-(1,3-tiazolin-2-yl)azetidin-derivater | |
ES2157214T3 (es) | Procedimiento para producir derivados de azetidinona sustituidos en posicion 4. | |
ATE122334T1 (de) | 4-(4-alkoxyphenyl)-2-butylaminderivate und deren herstellungsverfahren. | |
DK1466905T3 (da) | Fremgangsmåde til fremstilling af en optisk aktiv oxoheptensyreester | |
IL119130A0 (en) | Production of optically active 2-halo-1- (substituted phenyl) ethanol and substituted styrene oxide | |
AU689459B2 (en) | Process for the preparation of aminotriazine derivatives | |
ES2060545A1 (es) | Un procedimiento para producir un derivado de benzo(b)tiofen-5-ilo opticamente activo. | |
ES2144327T3 (es) | Procedimiento para preparar un compuesto de 2-cianobifenilo. | |
ES2033313T3 (es) | Procedimiento de sintesis de azetidinonas. | |
DK11788D0 (da) | Stereobevarende syntese af 1-substituerede (s)- og (r)-2-aminometylpyrrolidiner og mellemprodukter dertil | |
PT916656E (pt) | Metodo para producao de derivados de pirrolidinona | |
FI942167A0 (fi) | Optisesti aktiivinen 1-fenyylipyrrolidonijohdannainen, välituote sen valmistamiseksi ja menetelmä molempien valmistamiseksi | |
WO2005046854A3 (en) | A process for the preparation of diphenylmethylsulfinyl derivatives | |
ES8404989A1 (es) | Un procedimiento para preparar 4-(2-hidroxietil)-2-azetidinona opticamente activa. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
Ref document number: 554455 Country of ref document: ES |