ES2079521T3 - Derivados del n-alfa-fluor-acriloilaminoacido, opticamente activos, su obtencion, los polimeros opticamente activos obtenidos a partir de ellos y su uso para la separacion de racematos. - Google Patents

Derivados del n-alfa-fluor-acriloilaminoacido, opticamente activos, su obtencion, los polimeros opticamente activos obtenidos a partir de ellos y su uso para la separacion de racematos.

Info

Publication number
ES2079521T3
ES2079521T3 ES91110142T ES91110142T ES2079521T3 ES 2079521 T3 ES2079521 T3 ES 2079521T3 ES 91110142 T ES91110142 T ES 91110142T ES 91110142 T ES91110142 T ES 91110142T ES 2079521 T3 ES2079521 T3 ES 2079521T3
Authority
ES
Spain
Prior art keywords
optically active
alpha
acid derivatives
fluor
obtaining
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
Application number
ES91110142T
Other languages
English (en)
Inventor
Rolf Dr Grosser
Walter Dr Lange
Bruno Dr Bomer
Dieter Prof Dr Arlt
Dietmar Dr Bielefeldt
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.)
Bayer AG
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
Application granted granted Critical
Publication of ES2079521T3 publication Critical patent/ES2079521T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/30—Processes for preparing, regenerating, or reactivating
    • B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
    • B01J20/3242—Layers with a functional group, e.g. an affinity material, a ligand, a reactant or a complexing group
    • B01J20/3268—Macromolecular compounds
    • B01J20/327—Polymers obtained by reactions involving only carbon to carbon unsaturated bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08—Selective adsorption, e.g. chromatography
    • B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
    • B01D15/38—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 - B01D15/36
    • B01D15/3833—Chiral chromatography
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26—Synthetic macromolecular compounds
    • B01J20/261—Synthetic macromolecular compounds obtained by reactions only involving carbon to carbon unsaturated bonds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/26—Synthetic macromolecular compounds
    • B01J20/265—Synthetic macromolecular compounds modified or post-treated polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
    • B01J20/282—Porous sorbents
    • B01J20/285—Porous sorbents based on polymers
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
    • B01J20/29—Chiral phases
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00—Carboxylic acid amides
    • C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
    • C07C233/49—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F20/00—Homopolymers and copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F20/02—Monocarboxylic acids having less than ten carbon atoms, Derivatives thereof
    • C08F20/52—Amides or imides
    • C08F20/54—Amides, e.g. N,N-dimethylacrylamide or N-isopropylacrylamide
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2220/00—Aspects relating to sorbent materials
    • B01J2220/50—Aspects relating to the use of sorbent or filter aid materials
    • B01J2220/54—Sorbents specially adapted for analytical or investigative chromatography
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/14—The ring being saturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00—Systems containing two condensed rings
    • C07C2602/36—Systems containing two condensed rings the rings having more than two atoms in common
    • C07C2602/42—Systems containing two condensed rings the rings having more than two atoms in common the bicyclo ring system containing seven carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Pyridine Compounds (AREA)

Abstract

LA INVENCION CONSISTE EN NUEVOS DERIVADOS OPTICO-ACTIVOS DE ACIDO ACRILAMINO N-ALFA-FLUORADO DE LA FORMULA GENERAL: EN LA QUE R SUB 1, R SUB 2, R SUB 3 Y X TIENEN EN LA DESCRIPCION EL SIGNIFICADO INDICADO, UN PROCEDIMIENTO PARA SU OBTENCION, SU POLIMERIZACION A POLIMEROS OPTICO-ACTIVOS Y LA UTILIZACION DE ESTOS POLIMEROS COMO ADSORBIENTES PARA LA SEPARACION CROMATOGRAFICA DE RACEMATOS EN SUS ENANTIOMEROS.
ES91110142T 1990-07-03 1991-06-20 Derivados del n-alfa-fluor-acriloilaminoacido, opticamente activos, su obtencion, los polimeros opticamente activos obtenidos a partir de ellos y su uso para la separacion de racematos. Expired - Lifetime ES2079521T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE4021108A DE4021108A1 (de) 1990-07-03 1990-07-03 Optisch aktive n-(alpha)-fluoracryloyl-aminosaeure-derivate, ihre herstellung, die daraus hergestellten optisch aktiven polymeren und deren verwendung zur spaltung von racematen

Publications (1)

Publication Number Publication Date
ES2079521T3 true ES2079521T3 (es) 1996-01-16

Family

ID=6409542

Family Applications (1)

Application Number Title Priority Date Filing Date
ES91110142T Expired - Lifetime ES2079521T3 (es) 1990-07-03 1991-06-20 Derivados del n-alfa-fluor-acriloilaminoacido, opticamente activos, su obtencion, los polimeros opticamente activos obtenidos a partir de ellos y su uso para la separacion de racematos.

Country Status (9)

Country Link
US (2) US5354884A (es)
EP (1) EP0464488B1 (es)
JP (1) JP2965752B2 (es)
AT (1) ATE128457T1 (es)
CA (1) CA2045972C (es)
DE (2) DE4021108A1 (es)
DK (1) DK0464488T3 (es)
ES (1) ES2079521T3 (es)
GR (1) GR3017541T3 (es)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4221711A1 (de) * 1992-07-02 1994-01-05 Bayer Ag Optisch aktive Aminosäuresulfoxid- und sulfon-Derivate, ihre Herstellung, ihre Polymerisation und Verwendung als Adsorbentien für die chromatographische Racematspaltung
DE4228135A1 (de) * 1992-08-25 1994-03-03 Bayer Ag Polymerisierbare Dipeptide, Synthese, Polymerisation und Verwendung der Polymere zur chromatographischen Enantiomerentrennung
SE9203646L (sv) 1992-12-03 1994-05-24 Eka Nobel Ab Kirala adsorbenter och framställning av dessa samt föreningar på vilka adsorbenterna är baserade och framställning av dessa föreningar
JPH11507402A (ja) * 1995-05-26 1999-06-29 アイジェン・インコーポレーテッド 分子的にインプリントされた粒状ポリマー及び同ポリマーのペルフロオロカーボン液中における安定化懸濁重合
DE19546136A1 (de) * 1995-12-11 1997-06-12 Bayer Ag Chirale stationäre Phasen für die chromatographische Trennung von optischen Isomeren
US5994560A (en) * 1996-08-29 1999-11-30 Hoechst Celanese Corp. Resolution of racemic mixtures using polymers containing chiral units
US7854924B2 (en) * 2004-03-30 2010-12-21 Relypsa, Inc. Methods and compositions for treatment of ion imbalances
EA201892366A1 (ru) 2016-04-18 2019-03-29 Сарепта Терапьютикс, Инк. Антисмысловые олигомеры и способы их применения для лечения заболеваний, связанных с геном кислой альфа-глюкозидазы

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL6509157A (es) * 1964-07-24 1966-01-25
US3452182A (en) * 1964-07-24 1969-06-24 Polaroid Corp Photographic products and processes
CH618320A5 (es) * 1975-09-30 1980-07-31 Ciba Geigy Ag
AU543804B2 (en) * 1980-10-31 1985-05-02 Takeda Chemical Industries Ltd. Amides having bicyclic substituents on nitrogen
JPS62164692A (ja) * 1986-01-14 1987-07-21 Nippon Kayaku Co Ltd α−アスパルチル−フエニルアラニンエステルの新しい製造法
DE3706890A1 (de) * 1987-03-04 1988-09-15 Bayer Ag Optisch aktive (meth)acrylamide, verfahren zu ihrer herstellung und ihre verwendung zur racematspaltung
JPS63270652A (ja) * 1987-04-30 1988-11-08 Nippon Kayaku Co Ltd β−アスパルテ−ムの製造法
EP0379917B1 (de) * 1989-01-26 1995-08-09 Bayer Ag Optisch aktive (Meth)Acrylsäure-Derivate, ihre Herstellung, ihre Polymerisation zu optisch aktiven Polymeren und deren Verwendung

Also Published As

Publication number Publication date
CA2045972A1 (en) 1992-01-04
EP0464488A2 (de) 1992-01-08
JPH04230350A (ja) 1992-08-19
EP0464488A3 (en) 1993-07-14
GR3017541T3 (en) 1995-12-31
US5354884A (en) 1994-10-11
EP0464488B1 (de) 1995-09-27
JP2965752B2 (ja) 1999-10-18
DK0464488T3 (da) 1996-02-12
DE4021108A1 (de) 1992-01-09
US5292924A (en) 1994-03-08
CA2045972C (en) 2003-08-19
ATE128457T1 (de) 1995-10-15
DE59106571D1 (de) 1995-11-02

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