ES2000299A6 - Procedimiento para la preparaciom de nuevos derivados de n-aralquil-piperinmetanol - Google Patents

Procedimiento para la preparaciom de nuevos derivados de n-aralquil-piperinmetanol

Info

Publication number
ES2000299A6
ES2000299A6 ES8600071A ES8600071A ES2000299A6 ES 2000299 A6 ES2000299 A6 ES 2000299A6 ES 8600071 A ES8600071 A ES 8600071A ES 8600071 A ES8600071 A ES 8600071A ES 2000299 A6 ES2000299 A6 ES 2000299A6
Authority
ES
Spain
Prior art keywords
aralkyl
derivatives
piperidinemethanol derivatives
relates
aralkyl piperidinemethanol
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
Application number
ES8600071A
Other languages
English (en)
Inventor
Albert A Carr
Norbert L Wiech
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.)
Aventis Pharmaceuticals Inc
Original Assignee
Merrell Dow Pharmaceuticals 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
Application filed by Merrell Dow Pharmaceuticals Inc filed Critical Merrell Dow Pharmaceuticals Inc
Publication of ES2000299A6 publication Critical patent/ES2000299A6/es
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/22—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/04—Anorexiants; Antiobesity agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/06—Antiarrhythmics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Abstract

ESTA INVENCION SE REFIERE A UNA NUEVA CLASE DE COMPUESTOS CON IMPORTANTES PROPIEDADES BIOQUIMICAS Y FARMACOLOGICAS. MAS ESPECIALMENTE, ESTA INVENCION SE REFIERE A DERIVADOS DE N-ARALQUIL-PIPERIFINMETANOL QUE SON POTENTES Y SELECTIVOS INHIBIDORES DE LA UNION DE LA SEROTONINA AL SITIO RECEPTOR 5HT2 Y A PROCEDIMIENTOS PARA SU PREPARACION Y USO. LOS COMPUESTOS DE ESTAINVENCION SON PRESENTADOS POR LA FORMULA:SUS ISOMEROS OPTICOSY SUS MEZCLAS Y SUS SALES FARMACEUTICAMENTE ACEPTABLES, DONDEN ES 2, 3 O 4 Y CADA GRUPO R Y R1 REPRESENTA INDEPENDIENTEMENTE HIDROGENO, ALQUILO C1-6, HALOGENO, TRIFLUORMETILO, HIDROXI, ALCOXI C1-6 O AMINO. REPRESENTATIVOS DE LOS SUSTITUYENTES RY R1 PARA ALQUILO C1-6 SON METILO, ETILO, PROPILO, ISOPROPILO, N-BUTILO, T-BUTILO, PENTILO, HEXILO, CICLOPROPILO Y CICLOPENTILO, SIENDO PREFERIDOS METILO Y ETILO. ESTAN COMPRENDIDOS TODOS LOS HALOGENOS, SIENDO PREFERIDOS FLUOR Y CLORO. REPRESENTATIVOS DE LOS SUSTITUYENTES ALCOXI C1-6 SON METOXI, ETOXI.
ES8600071A 1985-07-02 1986-07-01 Procedimiento para la preparaciom de nuevos derivados de n-aralquil-piperinmetanol Expired ES2000299A6 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US75141985A 1985-07-02 1985-07-02

Publications (1)

Publication Number Publication Date
ES2000299A6 true ES2000299A6 (es) 1988-02-16

Family

ID=25021900

Family Applications (1)

Application Number Title Priority Date Filing Date
ES8600071A Expired ES2000299A6 (es) 1985-07-02 1986-07-01 Procedimiento para la preparaciom de nuevos derivados de n-aralquil-piperinmetanol

Country Status (21)

Country Link
EP (1) EP0208235B1 (es)
JP (1) JPH0655720B2 (es)
KR (1) KR900001184B1 (es)
CN (1) CN1023895C (es)
AR (2) AR241904A1 (es)
AT (1) ATE49403T1 (es)
AU (1) AU590582B2 (es)
CA (1) CA1280421C (es)
DE (1) DE3668167D1 (es)
DK (1) DK174153B1 (es)
ES (1) ES2000299A6 (es)
FI (1) FI84474C (es)
GR (1) GR861699B (es)
HU (1) HU196058B (es)
IE (1) IE58460B1 (es)
IL (1) IL79266A (es)
NO (1) NO167384C (es)
NZ (1) NZ216689A (es)
PH (1) PH22141A (es)
PT (1) PT82890B (es)
ZA (1) ZA864772B (es)

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KR910006138B1 (ko) * 1986-09-30 1991-08-16 에자이 가부시끼가이샤 환상아민 유도체
ZA888572B (en) * 1987-11-23 1989-08-30 Merrell Dow Pharma Treatment of fibromyalgia
JPH02138214A (ja) * 1987-12-10 1990-05-28 Merrell Dow Pharmaceut Inc 不安を治療する方法
US5093341A (en) * 1987-12-17 1992-03-03 Merrell Dow Pharmaceuticals Inc. N-aralkyl piperidine derivatives useful as antithrombolytic agents
EP0325063B1 (en) * 1988-01-21 1994-03-09 Merrell Dow Pharmaceuticals Inc. Use of 1,4-disubstituted-piperidinyl compounds in the manufacture of a medicament for the treatment of insomnia
ZA891901B (en) * 1988-03-17 1989-11-29 Merrell Dow Pharma Method for the treatment of the extrapyramidal side effects associated with neuroleptic therapy
JP2969359B2 (ja) * 1989-01-13 1999-11-02 武田薬品工業株式会社 環状アミン化合物
US5032598A (en) * 1989-12-08 1991-07-16 Merck & Co., Inc. Nitrogens containing heterocyclic compounds as class III antiarrhythmic agents
ZA9010081B (en) * 1989-12-20 1991-10-30 Merrell Dow Pharma Method for the treatment of glaucoma
JP2758050B2 (ja) * 1989-12-27 1998-05-25 株式会社トクヤマ 土質安定用薬液およびその注入工法
US6004980A (en) * 1990-06-01 1999-12-21 Merrell Pharmaceuticals, Inc. (+)-α-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol
AU652759B2 (en) * 1990-06-01 1994-09-08 Aventisub Ii Inc. (+)-alpha-(2,3-dimethoxyphenyl)-1-(2-(4-fluorophenyl)ethyl)- 4-piperidinemethanol
JPH07111050B2 (ja) * 1990-12-12 1995-11-29 株式会社親和テクノ セメントグラウトを用いた地盤注入工法
FR2672286B1 (fr) * 1991-01-31 1994-11-18 Synthelabo Derives de 1-(4-chlorophenyl)-2-[4-(phenylmethyl)piperidin-1-yl]ethanol, leur preparation et leur application en therapeutique.
ZA929008B (en) * 1991-12-13 1993-05-21 Bristol Myers Squibb Co Piperazinyl- and piperidinyl-cyclohexanols.
AU4659793A (en) * 1992-06-30 1994-01-24 United States Of America, Represented By The Secretary, Department Of Health And Human Services, The Anorectic epinephrine derivatives
FR2696741B1 (fr) * 1992-10-12 1994-11-25 Synthelabo Dérivés de 1-(4-chlorophényl)-2-[4-[(4-fluorophényl)méthyl]piperidin-1-yl] éthanol, leur préparation et leur application en thérapeutique.
CA2108245A1 (en) * 1992-11-04 1994-05-05 Gary J. Grover Method for treating myocardial ischemia employing serotonin receptor antagonists
EP0661266A1 (en) * 1993-12-27 1995-07-05 Toa Eiyo Ltd. Substituted cyclic amine compounds as 5HT2 antagonists
WO1997022583A1 (de) * 1995-12-20 1997-06-26 Eckhart Pein Neue 1-phenylalkyl/alkylen-4-(.alpha.-hydroxydiphenylmethyl)-piperidin derivate und ihre verwendung als serotonin antagonisten
US6028083A (en) * 1997-07-25 2000-02-22 Hoechst Marion Roussel, Inc. Esters of (+)-α-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl) ethyl]-4-piperidinemethanol
TWI249526B (en) * 1998-03-13 2006-02-21 Aventis Pharma Inc Novel processes for the preparation of (R)-alpha-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol
US6713627B2 (en) 1998-03-13 2004-03-30 Aventis Pharmaceuticals Inc. Processes for the preparation of (R)-α-(2,3-dimethoxyphenyl)-1-[2-(4-fluorophenyl)ethyl]-4-piperidinemethanol
SE9801516D0 (sv) * 1998-04-30 1998-04-30 Maria Carlsson M100907/4-Piperidinemethanol derivatives for autism
DE19934432A1 (de) 1999-07-22 2001-02-01 Merck Patent Gmbh Indolderivate
DE19939756A1 (de) * 1999-08-21 2001-02-22 Merck Patent Gmbh Piperidinalkohole
US7345096B2 (en) 2002-10-15 2008-03-18 Wyeth Use of norepinephrine reuptake modulators for preventing and treating vasomotor symptoms
US7491723B2 (en) 2003-10-14 2009-02-17 Wyeth Alkanol and cycloalkanol-amine derivatives and methods of their use
US7550485B2 (en) 2003-10-14 2009-06-23 Wyeth Substituted N-heterocycle derivatives and methods of their use
US7402698B2 (en) 2003-10-14 2008-07-22 Wyeth Secondary amino-and cycloamino-cycloalkanol derivatives and methods of their use
US7365076B2 (en) 2003-10-14 2008-04-29 Wyeth Substituted aryl cycloalkanol derivatives and methods of their use
US7531543B2 (en) 2003-10-14 2009-05-12 Wyeth Phenylpiperazine cycloalkanol derivatives and methods of their use
US7419980B2 (en) 2003-10-14 2008-09-02 Wyeth Fused-aryl and heteroaryl derivatives and methods of their use
US7524846B2 (en) 2003-10-14 2009-04-28 Wyeth Arylalkyl- and cycloalkylalkyl-piperazine derivatives and methods of their use
ES2515092T3 (es) 2003-12-11 2014-10-29 Sunovion Pharmaceuticals Inc. Combinación de un sedante y un modulador neurotransmisor y métodos de mejorar la calidad del sueño y de tratar la depresión
DE102004010132A1 (de) * 2004-02-27 2005-09-15 Merck Patent Gmbh Piperidinderivate
US7414052B2 (en) 2004-03-30 2008-08-19 Wyeth Phenylaminopropanol derivatives and methods of their use
US7517899B2 (en) 2004-03-30 2009-04-14 Wyeth Phenylaminopropanol derivatives and methods of their use
US20060069124A1 (en) * 2004-09-07 2006-03-30 Rao P S Use of MDL-100,907 for treatment of allergic and eosinophil mediated diseases

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Publication number Priority date Publication date Assignee Title
US3100775A (en) * 1959-04-01 1963-08-13 Searle & Co alpha-phenyl(pyridyl or piperidyl)alkyl esters of (chloro or lower alkoxy)-benzoic acids and congeners
ZA717147B (en) * 1970-11-27 1972-07-26 Richardson Merrell Inc 4-(4-(alpha-hydroxybenzyl)piperidino)-4'-fluorobutyrophenone derivatives
SE7409245L (es) * 1973-07-19 1975-01-20 Robins Co Inc A H
FR2534580A1 (fr) * 1982-10-13 1984-04-20 Synthelabo Derives de phenyl-1 piperidino-2 propanol, leur preparation, et medicaments qui les contiennent
KR910006138B1 (ko) * 1986-09-30 1991-08-16 에자이 가부시끼가이샤 환상아민 유도체

Also Published As

Publication number Publication date
AR241904A1 (es) 1993-01-29
FI84474B (fi) 1991-08-30
HUT41387A (en) 1987-04-28
KR870001164A (ko) 1987-03-11
DK312386A (da) 1987-01-03
EP0208235B1 (en) 1990-01-10
FI84474C (fi) 1991-12-10
HU196058B (en) 1988-09-28
FI862801A0 (fi) 1986-07-01
IE861771L (en) 1987-01-02
NO862661D0 (no) 1986-07-01
ZA864772B (en) 1987-02-25
PT82890A (en) 1986-08-01
PT82890B (pt) 1988-05-27
DE3668167D1 (de) 1990-02-15
NO167384B (no) 1991-07-22
AU590582B2 (en) 1989-11-09
NO862661L (no) 1987-01-05
CN86104408A (zh) 1987-05-20
AR242184A1 (es) 1993-03-31
NO167384C (no) 1991-10-30
JPH0655720B2 (ja) 1994-07-27
CA1280421C (en) 1991-02-19
GR861699B (en) 1986-10-31
ATE49403T1 (de) 1990-01-15
KR900001184B1 (ko) 1990-02-27
EP0208235A1 (en) 1987-01-14
FI862801A (fi) 1987-01-03
NZ216689A (en) 1989-07-27
IL79266A (en) 1990-04-29
DK312386D0 (da) 1986-07-01
JPS625955A (ja) 1987-01-12
IE58460B1 (en) 1993-09-22
DK174153B1 (da) 2002-07-29
AU5931886A (en) 1987-01-08
PH22141A (en) 1988-06-01
CN1023895C (zh) 1994-03-02

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 20060703