PE75499A1 - Proceso para producir eteres de oxima (z)-azabiciclo en un unico recipiente - Google Patents

Proceso para producir eteres de oxima (z)-azabiciclo en un unico recipiente

Info

Publication number
PE75499A1
PE75499A1 PE1998000052A PE00005298A PE75499A1 PE 75499 A1 PE75499 A1 PE 75499A1 PE 1998000052 A PE1998000052 A PE 1998000052A PE 00005298 A PE00005298 A PE 00005298A PE 75499 A1 PE75499 A1 PE 75499A1
Authority
PE
Peru
Prior art keywords
mixture
azabicycle
eters
isomer
formula
Prior art date
Application number
PE1998000052A
Other languages
English (en)
Inventor
Mark A Schwindt
Lloyd C Franklin
Haile Tecle
Original Assignee
Warner Lambert Co
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 Warner Lambert Co filed Critical Warner Lambert Co
Publication of PE75499A1 publication Critical patent/PE75499A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/08Bridged systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Psychiatry (AREA)
  • Hospice & Palliative Care (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Indole Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

CARACTERIZADO PORQUE COMPRENDE a)HACER REACCIONAR UNA HIDROXILAMINA O-SUSTITUIDA DE FORMULA R-C�C-CH2-O-NH2, R ES ARIL o HETEROARIL C4-12 OPCIONALMENTE SUSTITUIDO POR ALCOXI, HALO, ENTRE OTROS; CON UNA AZABICICLOCETONA DE FORMULA (a), DONDE n ES 1-2 DE CONFIGURACION ESTEREOQUIMICA R, S, R/S CUANDO n ES 1; EN UNA SOLUCION ACUOSA LIBRE DE SOLVENTES ORGANICOS PARA FORMAR UNA MEZCLA DE ISOMEROS Z Y E DE ETER DE AZABICICLOOXIMA SUSTITUIDO POR -CH2-C�C-R; b)ANADIR UNO o MAS ACIDOS COMO ACIDO ORGANICO O MINERAL PARA ENRIQUECER LA MEZCLA EN EL ISOMERO Z; c)ELEVAR EL pH DE LA MEZCLA EN PARTICULAR A UN pH QUE SEA MAYOR DE 9, EFECTIVO PARA LIBERAR LA BASE LIBRE DE OXIMA; d)EXTRAER LA BASE LIBRE CON UN SOLVENTE NO ACUOSO, EN PARTICULAR ETER METIL TERBUTILICO; e)AISLAR EL ISOMERO Z ENRIQUECIDO AGREGANDO UN ACIDO EN PARTICULAR EL ACIDO BENZOICO OBTENIENDO PUREZAS SUPERIORES AL 98%
PE1998000052A 1997-01-27 1998-01-26 Proceso para producir eteres de oxima (z)-azabiciclo en un unico recipiente PE75499A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3597797P 1997-01-27 1997-01-27

Publications (1)

Publication Number Publication Date
PE75499A1 true PE75499A1 (es) 1999-08-20

Family

ID=21885887

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998000052A PE75499A1 (es) 1997-01-27 1998-01-26 Proceso para producir eteres de oxima (z)-azabiciclo en un unico recipiente

Country Status (21)

Country Link
US (1) US6121459A (es)
EP (1) EP1021446A1 (es)
JP (1) JP2001511127A (es)
KR (1) KR20000070464A (es)
AR (1) AR011775A1 (es)
AU (1) AU741566B2 (es)
BR (1) BR9714469A (es)
CA (1) CA2270884A1 (es)
CO (1) CO5011092A1 (es)
GT (1) GT199800019A (es)
HR (1) HRP980040B1 (es)
IL (1) IL129793A (es)
MY (1) MY132840A (es)
NZ (1) NZ335784A (es)
PA (1) PA8445601A1 (es)
PE (1) PE75499A1 (es)
SV (1) SV1998000003A (es)
TW (1) TW533215B (es)
UY (1) UY24857A1 (es)
WO (1) WO1998032758A1 (es)
ZA (1) ZA98618B (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5583592B2 (ja) * 2007-11-30 2014-09-03 ニューリンク ジェネティクス コーポレイション Ido阻害剤
FR2938534B1 (fr) 2008-11-14 2012-10-26 Sanofi Aventis Procede de preparation de l'hemifumarate d'eplivanserine

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4158015A (en) * 1978-08-16 1979-06-12 Mobil Oil Corporation Process for the stereoselective synthesis of the E isomer of aryl alkyl oximes
US5346911A (en) * 1990-03-06 1994-09-13 Warner-Lambert Company Azabicyclo and azacyclo oxime and amine cholinergic agents and methods of treatment
IL97266A0 (en) * 1990-03-06 1992-05-25 Warner Lambert Co Azabicyclo and azacyclo oximes and amines,their preparation and pharmaceutical compositions containing them
US5306718A (en) * 1990-03-06 1994-04-26 Warner-Lambert Company Oxime and amine substituted azabicyclo and azocyclo muscarinic agonists and methods of treatment
AU2782792A (en) * 1991-10-15 1993-05-21 Warner-Lambert Company Azabicyclo oxime and amine cholinergic agents and methods of treatment
DE4203170A1 (de) * 1992-02-05 1993-08-12 Basf Ag Verfahren zur herstellung von e-oximethern von phenylglyoxylsaeureestern
IL107881A0 (en) * 1992-12-05 1994-04-12 Fisons Corp Furanone derivatives and pharmaceutical compositions containing them
US5514812A (en) * 1994-06-10 1996-05-07 Warner-Lambert Company Preparation of stereochemically pure oximes with muscarinic activity

Also Published As

Publication number Publication date
SV1998000003A (es) 1998-08-13
PA8445601A1 (es) 2000-05-24
UY24857A1 (es) 1998-06-25
HRP980040A2 (en) 1998-10-31
BR9714469A (pt) 2000-05-16
NZ335784A (en) 2000-12-22
AU5806598A (en) 1998-08-18
HRP980040B1 (en) 2002-10-31
TW533215B (en) 2003-05-21
IL129793A (en) 2003-01-12
JP2001511127A (ja) 2001-08-07
AU741566B2 (en) 2001-12-06
US6121459A (en) 2000-09-19
CA2270884A1 (en) 1998-07-30
AR011775A1 (es) 2000-09-13
GT199800019A (es) 1999-07-20
MY132840A (en) 2007-10-31
WO1998032758A1 (en) 1998-07-30
KR20000070464A (ko) 2000-11-25
EP1021446A1 (en) 2000-07-26
ZA98618B (en) 1998-07-30
IL129793A0 (en) 2000-02-29
CO5011092A1 (es) 2001-02-28

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Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed