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AR038930A1 - Proceso para sintetizar n-arilpiperazinas con sustitucion con n'-1-(benzoil(2-piridil)amino)-2-propano quiral - Google Patents

Proceso para sintetizar n-arilpiperazinas con sustitucion con n'-1-(benzoil(2-piridil)amino)-2-propano quiral

Info

Publication number
AR038930A1
AR038930A1 ARP030100831A ARP030100831A AR038930A1 AR 038930 A1 AR038930 A1 AR 038930A1 AR P030100831 A ARP030100831 A AR P030100831A AR P030100831 A ARP030100831 A AR P030100831A AR 038930 A1 AR038930 A1 AR 038930A1
Authority
AR
Argentina
Prior art keywords
formula
compound
amino
chiral
propane
Prior art date
Application number
ARP030100831A
Other languages
English (en)
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
Application filed by Wyeth Corp filed Critical Wyeth Corp
Publication of AR038930A1 publication Critical patent/AR038930A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/101,4-Dioxanes; Hydrogenated 1,4-dioxanes
    • C07D319/141,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
    • C07D319/161,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D319/18Ethylenedioxybenzenes, not substituted on the hetero ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)

Abstract

Un proceso para la formación de N-arilpiperazinas con cadenas laterales de N'-1-[benzoil(2-piridil)amino]-2-propano que tienen la estructura expuesta en la fórmula (1), donde * indica un centro quiral, y para la preparación de los compuestos intermediarios de las mismas. En este proceso, se introduce la quiralidad en el paso de formación del anillo de piperazina y se incorpora la sustitución con 2-aminopiridilo por medio de desplazamiento. Las piparazinas N,N'-disustituidas así obtenidas actúan sobre el sistema nervioso central como receptores de 5HT. Reivindicación 1: Un proceso para la preparación de un compuesto de la fórmula (2) en la cual: R es alquilo C1-3; Y representa una porción seleccionada entre el grupo que consiste en alcoxi C1-6, alquilo C1-6, cicloalquilo C3-7, cicloalcoxi C3-7; y Ar es 2,3-dihidro-benzodioxin-5-ilo o fenilo optativamente sustituido con hasta tres sustituyentes independientemente seleccionados entre halógeno, metoxi, halometilo, dihalometilo y trihalometilo; proceso que comprende los siguientes pasos: a) la reacción de un compuesto de la fórmula (3) con un 2-amino-1-alcanol(C3-5) quiral en un solvente aprótico polar para formar un compuesto de la fórmula (4) en la cual L representa un grupo saliente seleccionado entre Cl, Br, mesilato, triflato y tosilato y * indica un centro quiral; b) la conversión del compuesto de la fórmula (4) a un compuesto de la fórmula (5) en la cual X es Cl o Br; y c) el tratamiento del compuesto de la fórmula (5) con un compuesto de la fórmula (6) en un solvente aprótico, en la cual M es un metal alcalino, para producir el compuesto de fórmula (2).
ARP030100831A 2002-03-12 2003-03-11 Proceso para sintetizar n-arilpiperazinas con sustitucion con n'-1-(benzoil(2-piridil)amino)-2-propano quiral AR038930A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US36343102P 2002-03-12 2002-03-12

Publications (1)

Publication Number Publication Date
AR038930A1 true AR038930A1 (es) 2005-02-02

Family

ID=28041762

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP030100831A AR038930A1 (es) 2002-03-12 2003-03-11 Proceso para sintetizar n-arilpiperazinas con sustitucion con n'-1-(benzoil(2-piridil)amino)-2-propano quiral

Country Status (23)

Country Link
US (1) US6713626B2 (es)
EP (1) EP1483255B1 (es)
JP (1) JP4391241B2 (es)
KR (1) KR20040105765A (es)
CN (2) CN1982307A (es)
AR (1) AR038930A1 (es)
AT (1) ATE439356T1 (es)
AU (1) AU2003220094B2 (es)
BR (1) BR0308377A (es)
CA (1) CA2477892C (es)
CR (1) CR7431A (es)
DE (1) DE60328756D1 (es)
EC (1) ECSP045290A (es)
ES (1) ES2329122T3 (es)
IL (1) IL163827A0 (es)
MX (1) MXPA04008729A (es)
NO (1) NO20044050L (es)
NZ (1) NZ535168A (es)
RU (1) RU2315762C2 (es)
TW (1) TW200403231A (es)
UA (1) UA79273C2 (es)
WO (1) WO2003078417A1 (es)
ZA (1) ZA200408202B (es)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060287335A1 (en) * 2000-11-28 2006-12-21 Wyeth Serotonergic agents for treating sexual dysfunction
US20060223824A1 (en) * 2000-11-28 2006-10-05 Wyeth Serotonergic agents
JP5080716B2 (ja) * 2001-07-20 2012-11-21 サイコジェニックス・インコーポレーテッド 注意欠陥・多動性障害の治療
WO2003078420A2 (en) * 2002-03-12 2003-09-25 Wyeth Process for making chiral 1,4-disubstituted piperazines
US7361773B2 (en) * 2002-03-12 2008-04-22 Wyeth Preparation of N1-(2'-pyridyl)-1,2-propanediamine sulfamic acid and its use in the synthesis of biologically active piperazines
US7091349B2 (en) * 2002-03-12 2006-08-15 Wyeth Process for synthesizing N-aryl piperazines with chiral N′-1-[benzoyl(2-pyridyl)amino]-2-propane substitution
AU2003220122A1 (en) * 2002-03-12 2003-09-29 Wyeth Preparation of n1-(2'-pyridyl)-1,2-propanediamine sulfamic acid and its use in the synthesis of biologically active piperazines
US20050209245A1 (en) * 2004-03-19 2005-09-22 Wyeth Process for preparing N-aryl-piperazine derivatives
US20070099931A1 (en) * 2004-03-19 2007-05-03 Wyeth Pharmaceutical dosage forms and compositions
US20050215561A1 (en) * 2004-03-19 2005-09-29 Krishnendu Ghosh Pharmaceutical dosage forms and compositions
TW200700413A (en) * 2005-03-01 2007-01-01 Wyeth Corp Crystalline and amorphous 4-cyano-n-{(2r)-2-[4-(2,3-dihydro-benzo[1,4]dioxin-5-yl)-piperazin-1-yl]-propyl}-n-pyridin-2-yl-benzamide hydrochloride

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3586794T2 (de) 1984-12-21 1993-05-27 Duphar Int Res Arzneimittel mit psychotroper wirkung.
JPH01125357A (ja) 1987-11-06 1989-05-17 Dainippon Pharmaceut Co Ltd トリペプチドの誘導体
IL101722A (en) * 1991-05-02 1996-05-14 Wyeth John & Brother Ltd History of piperazine, their preparation and pharmaceutical preparations containing them
WO1994024115A1 (en) * 1993-04-16 1994-10-27 Santen Pharmaceutical Co., Ltd. Novel piperazine derivative
WO1995033725A1 (en) 1994-06-03 1995-12-14 John Wyeth & Brother Limited Novel processes and intermediates for the preparation of piperazine derivatives
GB9411099D0 (en) * 1994-06-03 1994-07-27 Wyeth John & Brother Ltd Piperazine derivatives
GB9413772D0 (en) * 1994-07-08 1994-08-24 Wyeth John & Brother Ltd 5-HT1A ligands
GB9514901D0 (en) * 1995-07-20 1995-09-20 American Home Prod Piperazine derivatives
JP2000508319A (ja) 1996-04-10 2000-07-04 メルク エンド カンパニー インコーポレーテッド αvβ3拮抗薬
US6469007B2 (en) 2000-11-28 2002-10-22 Wyeth Serotonergic agents

Also Published As

Publication number Publication date
BR0308377A (pt) 2005-01-11
RU2004130300A (ru) 2005-04-10
US6713626B2 (en) 2004-03-30
ATE439356T1 (de) 2009-08-15
TW200403231A (en) 2004-03-01
RU2315762C2 (ru) 2008-01-27
ES2329122T3 (es) 2009-11-23
NO20044050L (no) 2004-09-24
IL163827A0 (en) 2005-12-18
NZ535168A (en) 2006-03-31
DE60328756D1 (de) 2009-09-24
CA2477892A1 (en) 2003-09-25
MXPA04008729A (es) 2005-07-13
CR7431A (es) 2008-07-29
ZA200408202B (en) 2007-03-28
UA79273C2 (en) 2007-06-11
ECSP045290A (es) 2004-10-26
CN1642936A (zh) 2005-07-20
JP4391241B2 (ja) 2009-12-24
CN1982307A (zh) 2007-06-20
EP1483255B1 (en) 2009-08-12
CA2477892C (en) 2010-11-23
WO2003078417A1 (en) 2003-09-25
CN1304388C (zh) 2007-03-14
AU2003220094B2 (en) 2009-04-23
EP1483255A1 (en) 2004-12-08
US20030187265A1 (en) 2003-10-02
KR20040105765A (ko) 2004-12-16
JP2005526775A (ja) 2005-09-08
AU2003220094A1 (en) 2003-09-29

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