ES8600740A1 - Un procedimiento para la preparacion de nuevos derivados de isoindol - Google Patents

Un procedimiento para la preparacion de nuevos derivados de isoindol

Info

Publication number
ES8600740A1
ES8600740A1 ES533936A ES533936A ES8600740A1 ES 8600740 A1 ES8600740 A1 ES 8600740A1 ES 533936 A ES533936 A ES 533936A ES 533936 A ES533936 A ES 533936A ES 8600740 A1 ES8600740 A1 ES 8600740A1
Authority
ES
Spain
Prior art keywords
preparation
isoindole derivatives
piperidinyl
isoindole
oxoisoindole
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
ES533936A
Other languages
English (en)
Other versions
ES533936A0 (es
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.)
Bristol Myers Co
Original Assignee
Bristol Myers 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 Bristol Myers Co filed Critical Bristol Myers Co
Publication of ES533936A0 publication Critical patent/ES533936A0/es
Publication of ES8600740A1 publication Critical patent/ES8600740A1/es
Expired legal-status Critical Current

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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/08Vasodilators for multiple indications
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/12Antihypertensives
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic 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
    • C07D211/36Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Indole Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Suspension Of Electric Lines Or Cables (AREA)
  • Liquid Developers In Electrophotography (AREA)
  • Transformer Cooling (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

PROCEDIMIENTO PARA LA OBTENCION DE DERIVADOS DE ISOINDOL Y DE SUS SALES DE ADICION DE ACIDO FISIOLOGICAMENTE COMPATIBLES, DE FORMULA (I), EN LA QUE X ES HALOGENO O TRIFLUORMETILO; Y ES UN ENLACE SENCILLO O ALQUILENO DIVALENTE C1-4; Y R1 Y R2 PUEDEN SER VARIOS TIPOS DE RADICALES.CONSISTE EN LA REACCION DE UN COMPUESTO DE 4-AMINOPIPERIDINA DE FORMULA (II) CON UN COMPUESTO SULFANOILICO DE FORMULA (III), EN LAS QUE R3 Y R4 PUEDEN SER VARIOS TIPOS DE RADICALES Y LOS DEMAS SIMBOLOS TIENEN EL MISMO SIGNIFICADO QUE EN LA FORMULA (I). LA REACCION SE LLEVA A CABO EN UN DISOLVENTE INERTE, A LA TEMPERATURA DE REFLUJO DE LA MEZCLA DE REACCION.ESTOS COMPUESTOS TIENEN APLICACIONES FARMACOLOGICAS POR SUS PROPIEDADES DIURETICAS Y ANTIHIPERTENSIVAS.
ES533936A 1982-11-12 1984-07-02 Un procedimiento para la preparacion de nuevos derivados de isoindol Expired ES8600740A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/441,204 US4495194A (en) 1982-11-12 1982-11-12 Antihypertensive isoindole derivatives

Publications (2)

Publication Number Publication Date
ES533936A0 ES533936A0 (es) 1985-10-16
ES8600740A1 true ES8600740A1 (es) 1985-10-16

Family

ID=23751955

Family Applications (5)

Application Number Title Priority Date Filing Date
ES527146A Granted ES527146A0 (es) 1982-11-12 1983-11-10 Un procedimiento para la preparacion de nuevos derivados de isoindol.
ES533938A Expired ES8600742A1 (es) 1982-11-12 1984-07-02 Un procedimiento para la preparacion de nuevos derivados de isoindol
ES533939A Expired ES8600743A1 (es) 1982-11-12 1984-07-02 Un procedimiento de preparacion de nuevos derivados de 4-aminopiperidina
ES533937A Expired ES8600741A1 (es) 1982-11-12 1984-07-02 Un procedimiento para la preparacion de nuevos derivados de isoindol
ES533936A Expired ES8600740A1 (es) 1982-11-12 1984-07-02 Un procedimiento para la preparacion de nuevos derivados de isoindol

Family Applications Before (4)

Application Number Title Priority Date Filing Date
ES527146A Granted ES527146A0 (es) 1982-11-12 1983-11-10 Un procedimiento para la preparacion de nuevos derivados de isoindol.
ES533938A Expired ES8600742A1 (es) 1982-11-12 1984-07-02 Un procedimiento para la preparacion de nuevos derivados de isoindol
ES533939A Expired ES8600743A1 (es) 1982-11-12 1984-07-02 Un procedimiento de preparacion de nuevos derivados de 4-aminopiperidina
ES533937A Expired ES8600741A1 (es) 1982-11-12 1984-07-02 Un procedimiento para la preparacion de nuevos derivados de isoindol

Country Status (15)

Country Link
US (1) US4495194A (es)
EP (1) EP0111397B1 (es)
JP (2) JPS59101483A (es)
KR (1) KR870001168B1 (es)
AT (1) ATE40999T1 (es)
AU (2) AU566900B2 (es)
CA (1) CA1246081A (es)
DE (1) DE3379267D1 (es)
DK (2) DK165116C (es)
ES (5) ES527146A0 (es)
FI (1) FI82691C (es)
GR (1) GR81279B (es)
IE (1) IE56231B1 (es)
PT (1) PT77651B (es)
ZA (1) ZA838361B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU636164B2 (en) * 1982-11-12 1993-04-22 Bristol-Myers Squibb Company 2,3-dihydro-1-hydroxy-3-oxo-2-(1-substituted-4-piperidinyl)- 1N-isoindole derivatives
EP0351283A1 (fr) * 1988-07-12 1990-01-17 Synthelabo Dérivés de [(pipéridinyl-4) méthyl]-2 dihydro-2,3 1H-isoindole et tétrahydro-2,3,4,5 1H-benzazépines, leur préparation et leur application en thérapeutique
WO1991006297A1 (en) * 1989-10-27 1991-05-16 The Du Pont Merck Pharmaceutical Company (n-phthalimidoalkyl) piperidines
US5356906A (en) * 1989-10-27 1994-10-18 The Du Pont Merck Pharmaceutical Company (N-phthalimidoalkyl) piperidines useful as treatments for psychosis
JP2807577B2 (ja) * 1990-06-15 1998-10-08 エーザイ株式会社 環状アミド誘導体
ES2291293T3 (es) * 2000-02-29 2008-03-01 Mitsubishi Pharma Corporation Nuevos derivados amida ciclicos.
US8939859B2 (en) 2012-10-19 2015-01-27 Caterpillar Inc. Torque converter with stator clutch

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3579524A (en) * 1968-06-05 1971-05-18 Miles Lab 2-aminoalkyl derivatives of phthalimidines
GB1486104A (en) * 1975-01-23 1977-09-21 Wyeth John & Brother Ltd Phthalimidopiperidine derivatives
IL52413A (en) * 1977-06-29 1980-01-31 Teva Pharma Process for the preparazione of 5-chloro-6-sulfamyl-isoindolinone derivatives
SE7907121L (sv) * 1979-08-27 1981-02-28 Astra Laekemedel Ab Ftalimidinderivat

Also Published As

Publication number Publication date
KR840006643A (ko) 1984-12-01
DK165116B (da) 1992-10-12
JPH0450309B2 (es) 1992-08-13
AU2118383A (en) 1984-05-17
JPH051058A (ja) 1993-01-08
DE3379267D1 (en) 1989-04-06
FI834112A (fi) 1984-05-13
DK153690D0 (da) 1990-06-22
ATE40999T1 (de) 1989-03-15
ES533938A0 (es) 1985-10-16
DK517383D0 (da) 1983-11-11
ES8504172A1 (es) 1985-04-16
ES533939A0 (es) 1985-10-16
PT77651B (en) 1986-05-12
US4495194A (en) 1985-01-22
EP0111397B1 (en) 1989-03-01
ES533937A0 (es) 1985-10-16
DK517383A (da) 1984-05-13
KR870001168B1 (ko) 1987-06-15
DK153690A (da) 1990-06-22
EP0111397A1 (en) 1984-06-20
JPS59101483A (ja) 1984-06-12
ES8600743A1 (es) 1985-10-16
FI82691C (fi) 1991-04-10
PT77651A (en) 1983-12-01
CA1268767C (es) 1990-05-08
IE56231B1 (en) 1991-05-22
ES527146A0 (es) 1985-04-16
IE832638L (en) 1984-05-12
GR81279B (es) 1984-12-11
FI82691B (fi) 1990-12-31
CA1246081A (en) 1988-12-06
ES8600741A1 (es) 1985-10-16
ES8600742A1 (es) 1985-10-16
ZA838361B (en) 1984-06-27
AU604756B2 (en) 1991-01-03
DK165116C (da) 1993-03-01
FI834112A0 (fi) 1983-11-09
AU7936987A (en) 1988-01-14
AU566900B2 (en) 1987-11-05
ES533936A0 (es) 1985-10-16
JPH0545591B2 (es) 1993-07-09

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19970401