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ES8304062A1 - "procedimiento de preparacion de nuevos derivados 4-aminoetoxi-5-isopropil-2-metil". - Google Patents

"procedimiento de preparacion de nuevos derivados 4-aminoetoxi-5-isopropil-2-metil".

Info

Publication number
ES8304062A1
ES8304062A1 ES511220A ES511220A ES8304062A1 ES 8304062 A1 ES8304062 A1 ES 8304062A1 ES 511220 A ES511220 A ES 511220A ES 511220 A ES511220 A ES 511220A ES 8304062 A1 ES8304062 A1 ES 8304062A1
Authority
ES
Spain
Prior art keywords
aminoethoxy
medicines
isopropyl
derivatives
preparation
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
ES511220A
Other languages
English (en)
Other versions
ES511220A0 (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.)
Cortial SA
Original Assignee
Cortial SA
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
Priority claimed from FR8106832A external-priority patent/FR2503142A1/fr
Priority claimed from FR8203795A external-priority patent/FR2522654A2/fr
Priority claimed from FR8203796A external-priority patent/FR2522502A2/fr
Application filed by Cortial SA filed Critical Cortial SA
Publication of ES8304062A1 publication Critical patent/ES8304062A1/es
Publication of ES511220A0 publication Critical patent/ES511220A0/es
Granted legal-status Critical Current

Links

Classifications

    • 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
    • C07D319/201,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring with substituents attached to the hetero ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PROCEDIMIENTO PARA LA OBTENCION DE DERIVADOS DE 4-AMINOETOXI-5-ISOPROPIL-2-METIL FENOL, DE FORMULA (I), EN LA QUE R ES HIDROGENO O METILO Y R Y R PUEDEN SER VARIOS TIPOS DE RADICALES. CONSISTE EN LA REACCION DEL 5-ISOPROPIL-2-METIL-4-(N-4-METILAMINO ETOXI)FENOL CON EL CLORURO DEL ACIDO DE FORMULA R COOH, EN LA QUE R TIENE EL MISMO SIGNIFICADO QUE EN LA FORMULA (I), EN UN DISOLVENTE INERTE; SEGUIDA DE LA REDUCCION CON HIDRURO DE LITIO Y ALUMINIO EN UNA SUSPENSION EN ETER ETILICO, A LA TEMPERATURA DE REFLUJO. ESTOS COMPUESTOS TIENEN APLICACIONES FARMACOLOGICAS POR SU ACTIVIDAD ALFABLOQUEANTE Y ANTIAGREGANTE PLAQUETARIA.
ES511220A 1981-04-06 1982-04-06 "procedimiento de preparacion de nuevos derivados 4-aminoetoxi-5-isopropil-2-metil". Granted ES511220A0 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR8106832A FR2503142A1 (en) 1981-04-06 1981-04-06 N-Substd. 4-aminoethoxy-2-methyl-5-isopropyl-phenol derivs. - useful as alpha blockers and platelet aggregation inhibitors
FR8203795A FR2522654A2 (fr) 1982-03-04 1982-03-04 Nouveaux aminoethoxy-4 isopropyl-5 methyl-2 phenols diversement substitues, leur methode de synthese, les preparations pharmaceutiques les contenant et leur application en therapeutique
FR8203796A FR2522502A2 (fr) 1982-03-04 1982-03-04 Application d'aminoethoxy-4 isopropyl-5 methyl-2 phenols diversement substitues au traitement et a la prevention des thromboses

Publications (2)

Publication Number Publication Date
ES8304062A1 true ES8304062A1 (es) 1983-02-16
ES511220A0 ES511220A0 (es) 1983-02-16

Family

ID=27251046

Family Applications (1)

Application Number Title Priority Date Filing Date
ES511220A Granted ES511220A0 (es) 1981-04-06 1982-04-06 "procedimiento de preparacion de nuevos derivados 4-aminoetoxi-5-isopropil-2-metil".

Country Status (7)

Country Link
US (1) US4818772A (es)
EP (1) EP0062596B1 (es)
CA (1) CA1196650A (es)
DE (1) DE3264523D1 (es)
ES (1) ES511220A0 (es)
OA (1) OA07063A (es)
PT (1) PT74710B (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2570376B1 (fr) * 1984-09-19 1987-09-25 Cortial Nouveaux (isopropyl-5 (((methoxy-2 phenyl) piperazinyl)-2 ethoxy)-4 methyl-2 phenoxy)-1 alkylamino-3 propanols-2, leur methode de preparation et leur application therapeutique
FR2585355B2 (fr) * 1985-07-26 1988-11-25 Cortial Nouvelles n1-((aminoalcoxy)-4 isopropyl-5 methyl-2 phenoxy)-2 ethyl n4-phenyl piperazines, leur methode de preparation et leur application therapeutique
EP0179009A1 (fr) * 1984-09-19 1986-04-23 Cortial S.A. Nouvelles n1-(aminoalcoxy)-4 isopropyl-5 phénoxy)-2 éthyl n4-phényl pipérazines, leur méthode de préparation et leur application thérapeutique
FR2574401B1 (fr) * 1984-12-12 1987-01-09 Cortial Bis-((hydroxy-4 isopropyl-2 methyl-5 phenoxy)-2 ethyl) amines, leur methode de synthese, les preparations pharmaceutiques les contenant et leur application en therapeutique
FR2581643B1 (fr) * 1985-05-10 1988-11-18 Irceba Compositions pharmaceutiques utiles dans le domaine de l'urologie, contenant de l'acetoxy-1 methyl-2 ((piperidino)-2 ethoxy)-4 (methyl-1 ethyl)-5 benzene ou l'un de ses sels
FR2594122B1 (fr) * 1986-02-10 1988-06-10 Irceba ((pyrrolidinyl-1)-2 ethyoxy)-3 p cymene, les derives acetyl, acetoxy, hydroxy dudit produit et les medicaments contenant lesdits composes comme principe actif
EP0288647B1 (fr) * 1987-04-30 1992-04-08 INSTITUT DE RECHERCHES CHIMIQUES ET BIOLOGIQUES APPLIQUEES (I.R.C.E.B.A.) Société à responsabilité limitée dite: Dérivés du [(pyrrolidinyl-1)-2éthoxy]-5 p-cymène, le procédé de préparation desdits dérivés et les médicaments contenant lesdits dérivés
FR2614302B2 (fr) * 1986-02-10 1989-07-28 Irceba Derives du ((pyrrolidinul-1)-2 ethoxy)-5 p-cymene, procede pour leur preparation et medicaments en contenant.
FR2595357B1 (fr) * 1986-03-04 1988-07-08 Irceba (piperidino-3 propoxy)-5 p.cymene, les derives acetyl, acetoxy et hydroxy dudit produit, les sels de ces produits, un procede de preparation desdits produits et les medicaments contenant au moins un de ces produits comme principe actif
IT1224404B (it) * 1987-12-23 1990-10-04 Simes Composti attivi sul sistema cardiovascolare
JP2706755B2 (ja) * 1994-02-10 1998-01-28 日本たばこ産業株式会社 新規なベンジルアミノエトキシベンゼン誘導体
US6730691B1 (en) 2000-02-10 2004-05-04 Miles A. Galin Uses of alpha adrenergic blocking agents
EP1410808A4 (en) * 2001-07-02 2009-07-29 Santen Pharmaceutical Co Ltd MEDIUM FOR THE PROTECTION OF THE SEHNERV WITH ALPHA 1 RECEPTOR BLOCKER AS AN ACTIVE SUBSTANCE

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2688638A (en) * 1951-07-17 1954-09-07 Givaudan Corp Nu-(beta-phenoxyethyl) haloethylamines
US2688639A (en) * 1951-07-17 1954-09-07 Givaudan Corp Nu-(beta-phenoxyethyl) ethanolamines
GB745070A (en) * 1953-04-28 1956-02-22 Veritas Drug Company Ltd Improvements in or relating to basic thymol dimethyl-amino ethyl ethers
FR1310M (fr) * 1959-04-22 1962-05-14 Pfizer Agents thérapeutiques appartenant au groupe des anisoxyéthylamines.
GB902617A (en) * 1959-04-22 1962-08-01 Pfizer Ltd Improvements in or relating to therapeutically-active alkylamines
GB922600A (en) * 1960-05-06 1963-04-03 Crookes Lab Ltd Ortho-tertiary-butyl phenolethers
FR1405494A (fr) * 1963-06-20 1965-07-09 Ward Blenkinsop & Co Ltd 1.4-benzodioxannes et leur préparation
US3341572A (en) * 1965-05-26 1967-09-12 Warner Lambert Pharmaceutical Basic thymol n-ethyl-n-betahaloethyl-aminoethyl ethers
GB1301134A (en) * 1970-07-18 1972-12-29 Pfizer Ltd SUBSTITUTED 1-PHENYL-2-ALLYLAMINO-ALKANOLS, 1-PHENYL-2-ALLYLAMINO-ALKANES AND alpha-AMINOALKYLPHENYL KETONES
US3988475A (en) * 1974-02-05 1976-10-26 Istituto Luso Farmaco D'italia S.R.L. Phenoxyalkylamines
HU170392B (es) * 1974-07-19 1977-06-28
US4147805A (en) * 1978-07-28 1979-04-03 Mead Johnson & Company Alkylthiophenoxyalkylamines and the pharmaceutical use thereof
IT1209160B (it) * 1979-12-20 1989-07-10 Blasinachim Spa Processo per la sintesi di 4-[2-(dimetilammino)-etossi]2-metil-5-81-metiletil)-fenol-este ri

Also Published As

Publication number Publication date
PT74710A (fr) 1982-05-01
OA07063A (fr) 1984-01-31
PT74710B (fr) 1983-11-09
US4818772A (en) 1989-04-04
CA1196650A (fr) 1985-11-12
EP0062596B1 (fr) 1985-07-03
EP0062596A1 (fr) 1982-10-13
ES511220A0 (es) 1983-02-16
DE3264523D1 (en) 1985-08-08

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19970401