PE20050947A1 - Proceso para la sintesis de 3-(3-fluoro-4-hidroxifenil)-7-hidroxinaftonitrilo - Google Patents

Proceso para la sintesis de 3-(3-fluoro-4-hidroxifenil)-7-hidroxinaftonitrilo

Info

Publication number
PE20050947A1
PE20050947A1 PE2004000864A PE2004000864A PE20050947A1 PE 20050947 A1 PE20050947 A1 PE 20050947A1 PE 2004000864 A PE2004000864 A PE 2004000864A PE 2004000864 A PE2004000864 A PE 2004000864A PE 20050947 A1 PE20050947 A1 PE 20050947A1
Authority
PE
Peru
Prior art keywords
compound
formula
acid
approximately
bromine
Prior art date
Application number
PE2004000864A
Other languages
English (en)
Inventor
Yanzhong Wu
Jianxin Ren
Mousumi Ghosh
Mahmut Levent
Karen Sutherland
Panolil Raveendranath
Original Assignee
Wyeth Corp
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34312297&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20050947(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of PE20050947A1 publication Critical patent/PE20050947A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/54Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/53Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and hydroxy groups bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/01Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
    • C07C37/055Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis the substituted group being bound to oxygen, e.g. ether group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/18Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/24Preparation of ethers by reactions not forming ether-oxygen bonds by elimination of halogens, e.g. elimination of HCl

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pain & Pain Management (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Rheumatology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

SE REFIERE A UN PROCESO PARA ELABORAR UN COMPUESTO DE FORMULA (I), EN DONDE R1 ES CN, F O Cl; R2 ES H O Br; R3 Y R4 SON INDEPENDIENTEMENTE H O F, COMPRENDIENDO DICHO PROCESO EN HACER REACCIONAR UN COMPUESTO DE FORMULA (II) (3-BROMO,6-R2,1-R1,7-METOXINAFTILO) CON UN COMPUESTO DE FORMULA (IV) (ACIDO 3-R3,5-R4-4-METOXIFENILBORONICO) EN PRESENCIA DE Pd(PPh3)2Cl2 Y DME/AGUA Y EN PRESENCIA DE Na2CO3; EN DONDE PARA R1 SE PREFIERE CN; OBTENIENDOSE UN COMPUESTO DE FORMULA (V), EL CUAL SE CONVERTIRA EN EL COMPUESTO DE FORMULA I MEDIANTE LA REACCION CON BBr3 EN ClCH2CH2Cl, SEGUIDO DE TRATAMIENTO CON EtOH/H2O/C Y LA POSTERIOR CONVERSION DEL COMPUESTO DE FORMULA (I) EN UNA FORMA SALINA O ESTER. ADEMAS SE REFIERE A UN METODO PARA ELABORAR EL COMPUESTO DE FORMULA (II), QUE COMPRENDE EN CALENTAR EL COMPUESTO DE FORMULA (III) (8,3-DIBROMO-7-METOXINAFTONITRILO) CON CLORURO ESTANNOSO EN UNA MEZCLA DE ACIDO ACETICO Y ACIDO CLORHIDRICO CONCENTRADO A UNA TEMPERATURA APROXIMADA DE 100°C, ESTE COMPUESTO (III) FUE OBTENIDO POR DIBROMACION DEL 7-METOXI-1-NAFTONITRILO UTILIZANDO APROXIMADAMENTE 2 A 6 EQUIVALENTES DE BROMO EN ACIDO ACETICO A UNA TEMPERATURA APROXIMADA DE 40 A 70°C
PE2004000864A 2003-09-09 2004-09-07 Proceso para la sintesis de 3-(3-fluoro-4-hidroxifenil)-7-hidroxinaftonitrilo PE20050947A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US50170003P 2003-09-09 2003-09-09

Publications (1)

Publication Number Publication Date
PE20050947A1 true PE20050947A1 (es) 2005-12-13

Family

ID=34312297

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2004000864A PE20050947A1 (es) 2003-09-09 2004-09-07 Proceso para la sintesis de 3-(3-fluoro-4-hidroxifenil)-7-hidroxinaftonitrilo

Country Status (26)

Country Link
US (1) US7557237B2 (es)
EP (1) EP1663929A2 (es)
JP (1) JP2007505119A (es)
KR (1) KR20060088876A (es)
CN (1) CN1894185A (es)
AR (1) AR045613A1 (es)
AU (1) AU2004272571A1 (es)
BR (1) BRPI0413724A (es)
CA (1) CA2536768A1 (es)
CO (1) CO5670331A2 (es)
CR (1) CR8263A (es)
EC (1) ECSP066416A (es)
GT (1) GT200400179A (es)
IL (1) IL173922A0 (es)
MX (1) MXPA06002450A (es)
NI (1) NI200600063A (es)
NO (1) NO20061117L (es)
NZ (1) NZ569134A (es)
PA (1) PA8611901A1 (es)
PE (1) PE20050947A1 (es)
RU (1) RU2006105916A (es)
SG (1) SG146646A1 (es)
TW (1) TW200510280A (es)
UA (1) UA84166C2 (es)
WO (1) WO2005026105A2 (es)
ZA (1) ZA200601986B (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013122174A1 (ja) 2012-02-17 2013-08-22 旭硝子株式会社 含フッ素芳香族化合物及びその製造方法

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5554621A (en) 1995-06-07 1996-09-10 Bristol-Myers Squibb Company Dihydropyridine NPY antagonists: nitrogen heterocyclic derivatives
CA2264914A1 (en) 1996-09-13 1998-03-19 Mahmood Sabahi Production of 6-bromo-2-naphthol and derivatives
US5840996A (en) 1997-05-08 1998-11-24 Albemarle Corporation Production of brominated methoxynaphthalene compounds
US6914074B2 (en) 2001-12-13 2005-07-05 Wyeth Substituted phenyl naphthalenes as estrogenic agents

Also Published As

Publication number Publication date
PA8611901A1 (es) 2006-06-02
US20050054870A1 (en) 2005-03-10
GT200400179A (es) 2005-04-18
MXPA06002450A (es) 2006-06-20
CA2536768A1 (en) 2005-03-24
NI200600063A (es) 2006-06-21
EP1663929A2 (en) 2006-06-07
WO2005026105A2 (en) 2005-03-24
US7557237B2 (en) 2009-07-07
ZA200601986B (en) 2009-09-30
UA84166C2 (ru) 2008-09-25
TW200510280A (en) 2005-03-16
KR20060088876A (ko) 2006-08-07
NO20061117L (no) 2006-03-22
NZ569134A (en) 2009-10-30
CN1894185A (zh) 2007-01-10
BRPI0413724A (pt) 2006-10-17
CO5670331A2 (es) 2006-08-31
ECSP066416A (es) 2006-09-18
WO2005026105A3 (en) 2005-06-23
JP2007505119A (ja) 2007-03-08
IL173922A0 (en) 2006-07-05
RU2006105916A (ru) 2007-10-20
AR045613A1 (es) 2005-11-02
CR8263A (es) 2006-10-06
AU2004272571A1 (en) 2005-03-24
SG146646A1 (en) 2008-10-30

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