EP1635809A1 - Resolution de derives d'acide alpha-(phenoxy)phenylacetique - Google Patents

Resolution de derives d'acide alpha-(phenoxy)phenylacetique

Info

Publication number
EP1635809A1
EP1635809A1 EP04755657A EP04755657A EP1635809A1 EP 1635809 A1 EP1635809 A1 EP 1635809A1 EP 04755657 A EP04755657 A EP 04755657A EP 04755657 A EP04755657 A EP 04755657A EP 1635809 A1 EP1635809 A1 EP 1635809A1
Authority
EP
European Patent Office
Prior art keywords
acid
cpta
phenoxy
enantiomer
phenylacetic acid
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.)
Withdrawn
Application number
EP04755657A
Other languages
German (de)
English (en)
Other versions
EP1635809A4 (fr
Inventor
Edward D. Daugs
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.)
CymaBay Therapeutics Inc
Original Assignee
Metabolex Inc
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
Priority claimed from US10/656,567 external-priority patent/US7199259B2/en
Application filed by Metabolex Inc filed Critical Metabolex Inc
Publication of EP1635809A1 publication Critical patent/EP1635809A1/fr
Publication of EP1635809A4 publication Critical patent/EP1635809A4/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
    • C07C59/66Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings
    • C07C59/68Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings the non-carboxylic part of the ether containing six-membered aromatic rings the oxygen atom of the ether group being bound to a non-condensed six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/20Carboxylic acids, e.g. valproic acid having a carboxyl group bound to a chain of seven or more carbon atoms, e.g. stearic, palmitic, arachidic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/41Preparation of salts of carboxylic acids
    • C07C51/412Preparation of salts of carboxylic acids by conversion of the acids, their salts, esters or anhydrides with the same carboxylic acid part
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/58Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/64Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

L'invention concerne un procédé de production de composé d'acide alpha-(phénoxy)phénylacétique à enrichissement énantiomère, de formule (I), à partir de son mélange énantiomère, sachant que R1 est alkyle ou haloalkyle et que X est halogénure.
EP04755657A 2003-06-20 2004-06-18 Resolution de derives d'acide alpha-(phenoxy)phenylacetique Withdrawn EP1635809A4 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US60018903A 2003-06-20 2003-06-20
US10/656,567 US7199259B2 (en) 2003-06-20 2003-09-04 Resolution of α-(phenoxy)phenylacetic acid derivatives
PCT/US2004/019616 WO2004112774A1 (fr) 2003-06-20 2004-06-18 Resolution de derives d'acide ?lpha-(phenoxy)phenylacetique

Publications (2)

Publication Number Publication Date
EP1635809A1 true EP1635809A1 (fr) 2006-03-22
EP1635809A4 EP1635809A4 (fr) 2006-09-27

Family

ID=33544772

Family Applications (1)

Application Number Title Priority Date Filing Date
EP04755657A Withdrawn EP1635809A4 (fr) 2003-06-20 2004-06-18 Resolution de derives d'acide alpha-(phenoxy)phenylacetique

Country Status (7)

Country Link
EP (1) EP1635809A4 (fr)
KR (1) KR101073742B1 (fr)
CA (1) CA2529774C (fr)
IL (1) IL172663A0 (fr)
MX (1) MXPA05013981A (fr)
RS (1) RS20050937A (fr)
WO (1) WO2004112774A1 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7576131B2 (en) 1999-06-04 2009-08-18 Metabolex, Inc. Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes, hyperlipidemia and hyperuricemia
US6262118B1 (en) 1999-06-04 2001-07-17 Metabolex, Inc. Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes and hyperlipidemia
US7199259B2 (en) 2003-06-20 2007-04-03 Metabolex, Inc. Resolution of α-(phenoxy)phenylacetic acid derivatives
US20080194646A1 (en) * 2005-03-21 2008-08-14 Sanders Martin E Methods For Avoiding Edema in the Treatment of Metabolic, Inflammatory, and Cardiovascular Disorders
KR100678287B1 (ko) * 2005-06-23 2007-02-02 한미약품 주식회사 클로피도그렐의 제조방법 및 이에 사용되는 중간체
US7714131B2 (en) * 2005-09-23 2010-05-11 Metabolex, Inc. Process for the stereoselective preparation of (−)-halofenate and derivatives thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1182008A (en) * 1966-10-03 1970-02-25 Merck & Co Inc Resolution of d1-(3-Trifluoromethylphenoxy)-(4-Chlorophenyl)Acetic Acid
US3517050A (en) * 1966-10-03 1970-06-23 Merck & Co Inc Ester and amide derivative of (3-trifluoromethylphenoxy) (4 - halophenyl)acetic acid
WO2002044113A2 (fr) * 2000-11-28 2002-06-06 Metabolex, Inc. Utilisation de derives d'acide acetique(-)(3-halomethylphenoxy)(4-halophenyl) dans le traitement de la resistance a l'insuline, le diabete de type 2, l'hyperlipidemie et l'hyperuricemie

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6262118B1 (en) * 1999-06-04 2001-07-17 Metabolex, Inc. Use of (-) (3-trihalomethylphenoxy) (4-halophenyl) acetic acid derivatives for treatment of insulin resistance, type 2 diabetes and hyperlipidemia

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1182008A (en) * 1966-10-03 1970-02-25 Merck & Co Inc Resolution of d1-(3-Trifluoromethylphenoxy)-(4-Chlorophenyl)Acetic Acid
US3517050A (en) * 1966-10-03 1970-06-23 Merck & Co Inc Ester and amide derivative of (3-trifluoromethylphenoxy) (4 - halophenyl)acetic acid
WO2002044113A2 (fr) * 2000-11-28 2002-06-06 Metabolex, Inc. Utilisation de derives d'acide acetique(-)(3-halomethylphenoxy)(4-halophenyl) dans le traitement de la resistance a l'insuline, le diabete de type 2, l'hyperlipidemie et l'hyperuricemie

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of WO2004112774A1 *

Also Published As

Publication number Publication date
MXPA05013981A (es) 2006-03-02
KR101073742B1 (ko) 2011-10-13
RS20050937A (en) 2008-04-04
CA2529774A1 (fr) 2004-12-29
EP1635809A4 (fr) 2006-09-27
WO2004112774A1 (fr) 2004-12-29
IL172663A0 (en) 2006-04-10
KR20060030048A (ko) 2006-04-07
CA2529774C (fr) 2014-05-27

Similar Documents

Publication Publication Date Title
US20070203243A1 (en) Resolution of alpha-(phenoxy) phenylacetic acid derivatives
CA2623355C (fr) Resolution de derives d'acide alpha-(phenoxy) phenylacetique avec des naphtyl-alkylamines
US20080293965A1 (en) Process for the Dynamic Resolution of (Substituted) (R)- or (S)- Mandelic Acid
KR101073742B1 (ko) α-(페녹시)페닐아세트산 유도체의 분리
MXPA02005321A (es) Nuevo proceso para la preparacion de intermediarios enantiomericamente enriquecidos.
CA2623350C (fr) Procede de preparation stereoselective de (-)-halofenates et d'intermediaires de ces derniers
US5574183A (en) Preparation of optically active aliphatic carboxylic acids
JPH05229986A (ja) 2−(4−イソブチルフェニル)プロピオン酸の光学分割方法
US6812363B2 (en) Racemization of optically active 2-substituted phenyl glycine esters
US7619085B2 (en) Pyroglutamate salts and their use in the optical resolution of intermediates for the synthesis of dextrocetirizine and levocetirizine
CN100525757C (zh) α-(苯氧基)苯乙酸衍生物的拆分
US5977391A (en) (+)- and (-) -8-halogen-6- hydroxy-octanoic acid its salts and esters and process for making
US5869713A (en) (+)- or (-) -8-halogen-6-hydroxy-octanoic acid, its salts and esters, and process for making
US5041620A (en) Method for producing optically active 2-cyclopenten-4-one-1-ol esters, 2-cyclopenteno-4-one-1-ol ester and complexes thereof with optically active 1,6-diphenyl-2,4-hexadiyne-1,6-diol
JP2003238506A (ja) 光学活性なβ−フェニルアラニン誘導体の製造方法
JPH0267237A (ja) 光学活性1,1,1−トリフルオロ−2−アルカノールの製造法
JPH07215922A (ja) 1−アミノ−2−インダノール類の光学分割法

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20051223

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LI LU MC NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: HR MK

A4 Supplementary search report drawn up and despatched

Effective date: 20060830

RAX Requested extension states of the european patent have changed

Extension state: MK

Payment date: 20051223

Extension state: HR

Payment date: 20051223

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN

18D Application deemed to be withdrawn

Effective date: 20101231