ES2033203B1 - Procedimiento para la preparacion de intermediarios utiles para la sintesis de benzotiacepinas. - Google Patents

Procedimiento para la preparacion de intermediarios utiles para la sintesis de benzotiacepinas.

Info

Publication number
ES2033203B1
ES2033203B1 ES9101193A ES9101193A ES2033203B1 ES 2033203 B1 ES2033203 B1 ES 2033203B1 ES 9101193 A ES9101193 A ES 9101193A ES 9101193 A ES9101193 A ES 9101193A ES 2033203 B1 ES2033203 B1 ES 2033203B1
Authority
ES
Spain
Prior art keywords
preparation
procedure
benzotiacepines
synthesis
glicidico
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 - Fee Related
Application number
ES9101193A
Other languages
English (en)
Other versions
ES2033203A1 (es
Inventor
Luca Chirotto
Stefano Servi
Claudio Fuganti
Angelo Gentile
Claudio Giordano
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Zambon Group SpA
Zambon SpA
Original Assignee
Zambon Group SpA
Zambon SpA
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 Zambon Group SpA, Zambon SpA filed Critical Zambon Group SpA
Publication of ES2033203A1 publication Critical patent/ES2033203A1/es
Application granted granted Critical
Publication of ES2033203B1 publication Critical patent/ES2033203B1/es
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
    • C07D281/02—Seven-membered rings
    • C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
    • C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
    • C07D281/10—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02—Compounds containing oxirane rings
    • C07D303/48—Compounds containing oxirane rings 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, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02—Oxygen as only ring hetero atoms
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Genetics & Genomics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Epoxy Compounds (AREA)

Abstract

PROCEDIMIENTO PARA LA PREPARACION DE INTERMEDIARIOS UTILES PARA LA SINTESIS DE BENZOTIACEPINAS, TALES COMO ESTERES DE ACIDO (2R, 3S)-3-(4-METOXIFENIL)-GLICIDICO, DE FORMULA (I) EN DONDE R ES UN ALQUILO DE CSI1-CSI8 LINEAL O RAMIFICADO, UN CICLOALQUILO DE CSI5-CSI6, O UN GRUPO 2,2-DIMETIL-1, 3-DIOXOLAN-4-METILICO. EL PROCEDIMIENTO CONSISTE EN REALIZAR UNA TRANSESTERIFICACION ENZIMATICA DE MEZCLAS ENANTIOMERICAS DE ESTER METILICO O ETILICO DEL ACIDO (2R, 3S)-3-(4-METOXIFENIL)-GLICIDICO, Y SU (2R, 3S)-ENANTIOMERO (ENT-I), UTILIZANDO UN ALCOHOL DISTINTO DEL QUE FORMA PARTE DEL COMPUESTO (I) Y ANTI-I, EN PRESENCIA OPCIONAL DE UN DISOLVENTE APROPIADO, SEPARANDO FINALMENTE EL ESTER TRANESTERIFICADO. LA ENZIMA UTILIZADA PARA LA TRANSESTERIFICACION ENANTIOSELECTIVA ES UNA LIPASA DE ORIGEN ANIMAL O MICROBIANO O UNA ENZIMA PROTEOLITICA. ESTOS COMPUESTOS INTERMEDIOS SE USAN PARA LA PREPARACION DEL FARMACO DILTIAZEM, CON ACTIVIDAD VASODILATADORA CORONARIA.
ES9101193A 1990-05-17 1991-05-16 Procedimiento para la preparacion de intermediarios utiles para la sintesis de benzotiacepinas. Expired - Fee Related ES2033203B1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT02034890A IT1249777B (it) 1990-05-17 1990-05-17 Processo per la preparazione di intermedi per la sintesi del diltiazem

Publications (2)

Publication Number Publication Date
ES2033203A1 ES2033203A1 (es) 1993-03-01
ES2033203B1 true ES2033203B1 (es) 1993-12-16

Family

ID=11165937

Family Applications (1)

Application Number Title Priority Date Filing Date
ES9101193A Expired - Fee Related ES2033203B1 (es) 1990-05-17 1991-05-16 Procedimiento para la preparacion de intermediarios utiles para la sintesis de benzotiacepinas.

Country Status (13)

Country Link
US (2) US5571704A (es)
JP (2) JP3060187B2 (es)
AT (1) AT400446B (es)
BE (1) BE1005406A0 (es)
CA (1) CA2042535C (es)
CH (1) CH682670A5 (es)
DE (1) DE4115697C2 (es)
ES (1) ES2033203B1 (es)
FR (1) FR2662178B1 (es)
GB (2) GB2246351B (es)
IT (1) IT1249777B (es)
NL (1) NL194616C (es)
SE (1) SE509297C2 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2687789B2 (ja) * 1991-08-13 1997-12-08 田辺製薬株式会社 光学活性３−フェニルグリシッド酸エステル類化合物の製法
ES2048653B1 (es) * 1992-06-08 1994-12-16 Menarini Lab Proceso para la produccion de acido s-(+)-2-(3-benzoilfenil) propionico por transesterificacion enantioselectiva catalizada enzimaticamente en un disolvente organico.
ES2050067B1 (es) * 1992-06-08 1994-12-16 Menarini Lab Proceso para la produccion de acido s-(+)-2-(3-benzoilfenil) propionico por transesterificacion enantioselectiva con un alcohol bifuncional catalizada enzimaticamente en medio organico.
US6020174A (en) * 1992-07-27 2000-02-01 The Board Of Governors For Higher Education Chemoenzymatic synthesis of the taxol C-13 side chain N-benzolyl- (2R,3S)-Phenylisoserine
DE4225155C1 (es) * 1992-07-30 1993-08-05 Hoechst Ag, 6230 Frankfurt, De
SG72731A1 (en) * 1996-03-15 2000-05-23 Nabe Seiyaku Co Ltd Process for preparing optically active trans-3-phenylglycidamide compounds
IL123352A0 (en) * 1997-02-27 1998-09-24 Tanabe Seiyaku Co Process for preparing an optically active trans-3-substituted glycidic acid ester
CN1266430A (zh) * 1997-06-11 2000-09-13 田边制药株式会社 制备光学活性的苯基环氧乙烷化合物的方法
IT1302261B1 (it) 1998-09-24 2000-09-05 Zambon Spa Processo per la risoluzione cinetica enzimatica di 3-fenilglicidatiper transesterificazione con amminoalcoli
DE19901925A1 (de) * 1999-01-19 2000-07-27 Aventis Res & Tech Gmbh & Co Verfahren zur Trennung optischer Isomerer durch simultane Durchführung einer enzymatischen Reaktion und einer chromatographischen Trennung
CA2475094A1 (en) * 2002-02-06 2003-08-14 Commonwealth Scientific And Industrial Research Organisation Esterases with lipase activity
TWM583351U (zh) 2019-05-10 2019-09-11 北聯研磨科技股份有限公司 砂輪中心孔保護墊

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL8801311A (nl) * 1988-05-20 1989-12-18 Stamicarbon Fenylglycidaatstereoisomeren, omzettingsprodukten daarvan met 2-nitrothiofenol en de bereiding van diltiazem.
IT1217765B (it) * 1988-06-02 1990-03-30 Montedison Spa Processo per la risoluzione enzimatica degli isomeri ottici di derivati racemi esterei dell,acido 3 mercapto 2 alchilpropionico
IL91453A0 (en) * 1988-09-02 1990-04-29 Tanabe Seiyaku Co Preparation of optically active 3-phenyl-glycidic acid esters
DE3833774C1 (es) * 1988-10-05 1990-04-26 Fischer-Werke Artur Fischer Gmbh & Co Kg, 7244 Waldachtal, De
US5108916A (en) * 1989-06-05 1992-04-28 Rhone-Poulenc Rorer, S.A. Process for stereoselectively hydrolyzing, transesterifying or esterifying with immobilized isozyme of lipase from candida rugosa
US5244803A (en) * 1989-09-13 1993-09-14 Tanabe Seiyaku Co., Ltd. Process for preparing optically active 3-phenylglycidic acid esters
JPH0779706B2 (ja) * 1990-03-22 1995-08-30 田辺製薬株式会社 ２―クロロ―３―ヒドロキシ―３―フエニルプロピオン酸エステル類の製法
IT1240651B (it) * 1990-05-17 1993-12-17 Zambon Spa Processo per la risoluzione di derivati glicidici
FR2672600B1 (fr) * 1991-02-08 1994-10-14 Synthelabo Procede de preparation du (-)-(2r,3s)-2,3-epoxy-3-(4-methoxyphenyl) propionate de methyle.
NL9202208A (nl) * 1992-12-18 1994-07-18 Dsm Nv Werkwijze voor de enzymatische bereiding van optisch aktieve glycidezure esters.

Also Published As

Publication number Publication date
US6346632B1 (en) 2002-02-12
NL194616C (nl) 2002-09-03
FR2662178A1 (fr) 1991-11-22
IT9020348A0 (it) 1990-05-17
DE4115697C2 (de) 2000-09-07
AT400446B (de) 1995-12-27
IT1249777B (it) 1995-03-18
SE509297C2 (sv) 1999-01-11
GB2246351A (en) 1992-01-29
IT9020348A1 (it) 1991-11-17
CH682670A5 (it) 1993-10-29
SE9101482L (sv) 1991-11-18
GB2247020B (en) 1993-12-15
JP2000139492A (ja) 2000-05-23
CA2042535C (en) 1998-06-16
SE9101482D0 (sv) 1991-05-16
JP3223317B2 (ja) 2001-10-29
CA2042535A1 (en) 1991-11-18
DE4115697A1 (de) 1991-11-21
BE1005406A0 (fr) 1993-07-13
JPH04228095A (ja) 1992-08-18
US5571704A (en) 1996-11-05
ATA99591A (de) 1995-05-15
ES2033203A1 (es) 1993-03-01
JP3060187B2 (ja) 2000-07-10
NL9100854A (nl) 1991-12-16
GB9120710D0 (en) 1991-11-13
FR2662178B1 (fr) 1995-05-05
GB9110610D0 (en) 1991-07-03
GB2246351B (en) 1993-12-15
GB2247020A (en) 1992-02-19
NL194616B (nl) 2002-05-01

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 20050517