SI0617019T1 - Process for the preparation of 3R,5S-(+)-sodium-erythro-(E)-7-4-(4-fluorophenyl)--2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl-3,5-dihydroxy-hept-6-enoate - Google Patents

Process for the preparation of 3R,5S-(+)-sodium-erythro-(E)-7-4-(4-fluorophenyl)--2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl-3,5-dihydroxy-hept-6-enoate

Info

Publication number
SI0617019T1
SI0617019T1 SI9430308T SI9430308T SI0617019T1 SI 0617019 T1 SI0617019 T1 SI 0617019T1 SI 9430308 T SI9430308 T SI 9430308T SI 9430308 T SI9430308 T SI 9430308T SI 0617019 T1 SI0617019 T1 SI 0617019T1
Authority
SI
Slovenia
Prior art keywords
enoate
hept
fluorophenyl
diisopropyl
dihydroxy
Prior art date
Application number
SI9430308T
Other languages
English (en)
Slovenian (sl)
Inventor
Rolf Dr. Angerbauer
Rolf Dr. Grosser
Werner Dr. Miles Incorporated Hinsken
Joachim Dr. Rehse
Original Assignee
Bayer Ag
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
Application filed by Bayer Ag filed Critical Bayer Ag
Publication of SI0617019T1 publication Critical patent/SI0617019T1/xx

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/06Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/55Acids; Esters

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
SI9430308T 1993-03-24 1994-03-11 Process for the preparation of 3R,5S-(+)-sodium-erythro-(E)-7-4-(4-fluorophenyl)--2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl-3,5-dihydroxy-hept-6-enoate SI0617019T1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE4309553A DE4309553A1 (de) 1993-03-24 1993-03-24 Verfahren zur Herstellung von 3R,5S-(+)-Natrium-erythro-(E)-7-(4-(4-flurophenyl)-2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl)-3,5-dihydroxy-hept-6-enoat
EP94103776A EP0617019B1 (de) 1993-03-24 1994-03-11 Verfahren zur Herstellung von 3R,5S-(+)-Natrium-erythro-(E)-7-[4-(4-fluorphenyl)--2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl]-3,5-dihydroxy-hept-6-enoat

Publications (1)

Publication Number Publication Date
SI0617019T1 true SI0617019T1 (en) 2000-08-31

Family

ID=6483717

Family Applications (1)

Application Number Title Priority Date Filing Date
SI9430308T SI0617019T1 (en) 1993-03-24 1994-03-11 Process for the preparation of 3R,5S-(+)-sodium-erythro-(E)-7-4-(4-fluorophenyl)--2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl-3,5-dihydroxy-hept-6-enoate

Country Status (10)

Country Link
US (1) US5502199A (xx)
EP (1) EP0617019B1 (xx)
JP (1) JPH06321900A (xx)
AT (1) ATE193530T1 (xx)
DE (2) DE4309553A1 (xx)
DK (1) DK0617019T3 (xx)
ES (1) ES2148252T3 (xx)
GR (1) GR3034185T3 (xx)
PT (1) PT617019E (xx)
SI (1) SI0617019T1 (xx)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19714343A1 (de) 1997-04-08 1998-10-15 Bayer Ag Chromatographische Enantiomerentrennung von Lactonen
GT199800127A (es) * 1997-08-29 2000-02-01 Combinaciones terapeuticas.
US20080275104A1 (en) * 1997-11-25 2008-11-06 Musc Foundation For Research Development Methods of treating juvenile type 1 diabetes mellitus
US6291574B1 (en) 1999-08-27 2001-09-18 General Electric Company Polyester molded articles
SE9903028D0 (sv) * 1999-08-27 1999-08-27 Astra Ab New use
DE60022525T2 (de) * 1999-08-30 2006-06-14 Sanofi Aventis Deutschland Ramipril zur vorbeugung von kardiovaskulären vorfällen
AU2002219175A1 (en) * 2000-12-21 2002-07-01 Ciba Speciality Chemicals Holding Inc. Crystalline forms of cerivastatin sodium
DE10135013A1 (de) * 2001-07-18 2003-01-30 Bayer Ag Herstellung von Pyridylverbindungen
DE10216967A1 (de) * 2002-04-16 2003-11-13 Bayer Ag Verfahren zur Herstellung spezieller aromatischer Aldehyde
WO2005007110A2 (en) * 2003-07-11 2005-01-27 Pro-Pharmaceuticals, Inc. Compositions and methods for hydrophobic drug delivery
US20050037063A1 (en) * 2003-07-21 2005-02-17 Bolton Anthony E. Combined therapies
US20050053664A1 (en) * 2003-09-08 2005-03-10 Eliezer Zomer Co-administration of a polysaccharide with a chemotherapeutic agent for the treatment of cancer
WO2005079314A2 (en) * 2004-02-13 2005-09-01 Pro-Pharmaceuticals, Inc. Compositions and methods used to treat acne and candida
US20060211752A1 (en) 2004-03-16 2006-09-21 Kohn Leonard D Use of phenylmethimazoles, methimazole derivatives, and tautomeric cyclic thiones for the treatment of autoimmune/inflammatory diseases associated with toll-like receptor overexpression
US20110217412A1 (en) * 2004-07-30 2011-09-08 Jinis Biopharmaceuticals Co. Cholesterol lowering supplement and low cholesterol egg produced by using the same
KR100637762B1 (ko) * 2004-07-30 2006-10-23 주식회사 지니스 저콜레스테롤 란을 생산하기 위한 가금류용 사료첨가제 및 이를 이용한 저콜레스테롤 란의 생산방법
US20080286251A1 (en) * 2004-08-02 2008-11-20 Propharmaceuticals, Inc. Compositions and Methods for the Enhancement of Chemotherapy with Microbial Cytotoxins
WO2008112887A1 (en) * 2007-03-13 2008-09-18 Musc Foundation For Research Development Methods of treating juvenile type 1 diabetes mellitus
EP2161024A1 (de) 2008-09-05 2010-03-10 Universitätsklinikum Hamburg-Eppendorf Kombinationspräparat zur Behandlung von Krebs
JP6224624B2 (ja) 2012-02-02 2017-11-01 ザ・ユニバーシティ・オブ・シドニー 涙膜安定性における改善
KR101363119B1 (ko) 2012-05-08 2014-02-13 한남대학교 산학협력단 활성화 비닐 에스테르를 이용한 비닐 단량체의 합성방법
EP2986599A1 (en) 2013-04-17 2016-02-24 Pfizer Inc. N-piperidin-3-ylbenzamide derivatives for treating cardiovascular diseases
CN104031034B (zh) * 2014-07-01 2017-01-04 上海信谊百路达药业有限公司 一种匹伐他汀钙原料药中间体的制备方法
WO2016055901A1 (en) 2014-10-08 2016-04-14 Pfizer Inc. Substituted amide compounds
CN105622531A (zh) * 2015-04-03 2016-06-01 南京明德新药研发股份有限公司 轴手性异构体及其制备方法和制药用途
CA3125765A1 (en) 2019-01-18 2020-07-23 Astrazeneca Ab Pcsk9 inhibitors and methods of use thereof
WO2020243134A1 (en) 2019-05-27 2020-12-03 Immatics US, Inc. Viral vectors and their use in adoptive cellular therapy
DE102020111571A1 (de) 2020-03-11 2021-09-16 Immatics US, Inc. Wpre-mutantenkonstrukte, zusammensetzungen und zugehörige verfahren
TW202227616A (zh) 2020-08-21 2022-07-16 美商英麥提克斯股份有限公司 分離cd8+選擇t細胞的方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5169857A (en) * 1988-01-20 1992-12-08 Bayer Aktiengesellschaft 7-(polysubstituted pyridyl)-hept-6-endates useful for treating hyperproteinaemia, lipoproteinaemia or arteriosclerosis
US4906624A (en) * 1987-09-08 1990-03-06 Warner-Lambert Company 6-(((Substituted)pyridin-3-yl)alkyl)-and alkenyl)-tetrahydro-4-hydroxypyran-2-one inhibitors of cholesterol biosynthesis
NO177005C (no) * 1988-01-20 1995-07-05 Bayer Ag Analogifremgangsmåte for fremstilling av substituerte pyridiner, samt mellomprodukter til bruk ved fremstillingen
DE3905518A1 (de) * 1989-02-23 1990-10-11 Bayer Ag Substituierte phenoxyphenylpropionsaeure-derivate
US5177080A (en) * 1990-12-14 1993-01-05 Bayer Aktiengesellschaft Substituted pyridyl-dihydroxy-heptenoic acid and its salts

Also Published As

Publication number Publication date
ES2148252T3 (es) 2000-10-16
DE4309553A1 (de) 1994-09-29
ATE193530T1 (de) 2000-06-15
DK0617019T3 (da) 2000-10-23
EP0617019A1 (de) 1994-09-28
US5502199A (en) 1996-03-26
JPH06321900A (ja) 1994-11-22
DE59409378D1 (de) 2000-07-06
GR3034185T3 (en) 2000-11-30
EP0617019B1 (de) 2000-05-31
PT617019E (pt) 2000-11-30

Similar Documents

Publication Publication Date Title
SI0617019T1 (en) Process for the preparation of 3R,5S-(+)-sodium-erythro-(E)-7-4-(4-fluorophenyl)--2,6-diisopropyl-5-methoxymethyl-pyrid-3-yl-3,5-dihydroxy-hept-6-enoate
ES8701756A1 (es) Un metodo de preparacion de 6-2(pirrol-1-il sustituido) alquil piran-2-ona
ES2019899T4 (es) Procedimiento para preparar trans-6-6(2-3(3-o 4-carboxamido-sustituido-pirrol-1-il)-alquil)-4-hidroxipiran-2-onas con actividad inhibidora de la sintesis de colesterol.
EP0552041A3 (en) Enzymatic processes for resolution of enantiomeric mixtures of compounds useful as intermediates in the preparation of taxanes
DK1027343T3 (da) Fremgangsmåde til fremstilling af hydroxysubstituerede gamma-butyrolactoner
BR0210817A (pt) Método para a preparação de escitalopram, e, intermediário
Viso et al. Kinetic resolution of racemic disubstituted 1-pyrrolines via asymmetric reduction with a chiral titanocene catalyst
MX9806209A (es) Proceso para la preparacion de d-treo-(r,r)-metil fenidato y recirculacion de enantiomeros no deseados a traves de epimerizacion.
D'Oca et al. The addition of 2-tert-butyldimethylsilyloxyfuran to cyclic N-acyliminium ions containing cyclohexyl-based chiral auxiliaries
Jacobi et al. Enantioselective syntheses of (+)-and (−)-Phaseolinic acid
Tsuboi et al. Highly enantioselective reduction of 3-chloro-2-oxoalkanoates with fermenting bakers' yeast. A new synthesis of optically active 3-chloro-2-hydroxyalkanoates and glycidic esters
Gallos et al. A new strategy for the stereoselective synthesis of unnatural α-amino acids
ES2140778T3 (es) Procedimiento para la preparacion de compuestos de 2-cianoimidazol 1-sustituidos.
Suzuki et al. First systematic chiral syntheses of two pairs of enantiomers with 3, 5-dihydroxyheptenoic acid chain, associated with a potent synthetic statin NK-104
EP0983999A4 (en) METHOD FOR PRODUCING AMIDE DERIVATIVES AND THEIR INTERMEDIATE COMPOUNDS
Ribbons et al. (+)-Muconolactone from arene biotransformation in Pseudomonas putida: Production, absolute configuration and enantiomeric purity.
HU890364D0 (en) Process and apparatus for bird alarming
Bringmann et al. Atropo-enantioselective reduction of configurationally unstable biaryl lactones with BINAL-H
Chi-Nung et al. Enantioselective aldol reaction of chiral acyl thiazolidine thione derived boron enolates
CA2329210A1 (en) Process for preparation of enantiomerically pure n-methyl-n-[(1s)-1-phenyl-2((3s)-3-hydroxypyrrolidin-1-yl) ethyl]-2,2-diphenylacetamide
Futamura et al. Efficient route to (S)-azetidine-2-carboxylic acid
Endo et al. Photo-oxidation of L-tyrosine, an efficient 1, 4-chirality transfer reaction
Brózda et al. Transformation of (+)-thiomicamine into a new ligand for the enantioselective addition of methyllithium to prochiral imines
Boyce et al. Naturally occurring 4-methylthiazolines. A total synthesis of (−)-[4R, 4S′]-didehydromirabazole A
AU556793B2 (en) Sorbinil and methylsorbinil