ES412061A1 - Phenoxypropylamine derivatives and the preparation thereof - Google Patents

Phenoxypropylamine derivatives and the preparation thereof

Info

Publication number
ES412061A1
ES412061A1 ES73412061A ES412061A ES412061A1 ES 412061 A1 ES412061 A1 ES 412061A1 ES 73412061 A ES73412061 A ES 73412061A ES 412061 A ES412061 A ES 412061A ES 412061 A1 ES412061 A1 ES 412061A1
Authority
ES
Spain
Prior art keywords
group
moiety
alkyl
signifies
general formula
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
ES73412061A
Other languages
Spanish (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.)
Osterreichische Stickstoffwerke AG
Patheon Austria GmbH and Co KG
Original Assignee
Chemie Linz AG
Osterreichische Stickstoffwerke AG
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 Chemie Linz AG, Osterreichische Stickstoffwerke AG filed Critical Chemie Linz AG
Publication of ES412061A1 publication Critical patent/ES412061A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D303/00Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
    • C07D303/02Compounds containing oxirane rings
    • C07D303/12Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
    • C07D303/18Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
    • C07D303/20Ethers with hydroxy compounds containing no oxirane rings
    • C07D303/22Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • A61P9/10Drugs 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Procedure for obtaining phenoxypropyl amine derivatives, of general formula **(See formula)** wherein X signifies an alkylene moiety, possibly branched, R1 and R2, which may be the same or different, each signify a hydrogen atom, an alkyl, alkenyl, alkynyl, hydroxyalkyl, alkoxyalkyl, haloalkyl group, or aminoalkyl, a mono- or dialkylaminoalkyl group, an acylaminoalkyl or cyanoalkyl group or an aryl or aralkyl group, optionally substituted, R3 signifies an alkyl, alkenyl, alkenyloxy, alkoxy, acyl, cyano, nitro, amino or acylamino group, or a halogen atom, means an alkyl, preferably branched, residue, a hydroxyalkyl or cycloalkyl residue, and n is defined as 0 or as an integer from 1 to 3, as well as its pharmaceutically compatible acid addition salts, characterized in that a phenoxypropane derivative of general formula **(See formula)** where Y means the group (see graph), where Hal represents chlorine, bromine or iodine and R1, R2, R3, X and n have the definitions as in formula I, or a mixture of these compounds, in which Y has more than one of the indicated meanings, is reacted, at room temperature, or at a higher temperature, with ammonia or amines of general formula III H2n-R5 (III) in which R5 means hydrogen or the R4 moiety and the R5 moieties, possibly existing with the meaning of hydrogen, by reaction of the reaction product with a carbonyl compound of general formula IV **(See formula)** wherein R6 signifies a hydrogen atom or an alkyl moiety and R7 signifies an alkyl moiety, optionally substituted by hydroxy, or R6 and R7, together represent an alkylene moiety, by simultaneous reduction, or further, are transformed into the moiety R4 and the ketone groups, if any existing on the propoxy side chain, are simultaneously or subsequently reduced to the hydroxyl group and the bases obtained as reaction products are isolated as such or in the form of salts, or from The salts obtained are liberated from the bases and, if desired, transformed into pharmaceutically compatible salts. (Machine-translation by Google Translate, not legally binding)
ES73412061A 1972-02-28 1973-02-26 Phenoxypropylamine derivatives and the preparation thereof Expired ES412061A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
AT157372A AT321315B (en) 1972-02-28 1972-02-28 Process for the preparation of new ureidophenoxypropylamine derivatives and their salts

Publications (1)

Publication Number Publication Date
ES412061A1 true ES412061A1 (en) 1976-01-01

Family

ID=3516334

Family Applications (1)

Application Number Title Priority Date Filing Date
ES73412061A Expired ES412061A1 (en) 1972-02-28 1973-02-26 Phenoxypropylamine derivatives and the preparation thereof

Country Status (21)

Country Link
JP (1) JPS5626654B2 (en)
AT (1) AT321315B (en)
BE (1) BE796029A (en)
CH (1) CH577956A5 (en)
CS (1) CS168625B2 (en)
DD (1) DD105214A1 (en)
DE (1) DE2264182C3 (en)
DK (1) DK136185B (en)
ES (1) ES412061A1 (en)
FI (1) FI59582C (en)
FR (1) FR2173990B1 (en)
GB (1) GB1397663A (en)
HU (1) HU165235B (en)
IE (1) IE37271B1 (en)
LU (1) LU66869A1 (en)
NL (1) NL7300688A (en)
PL (1) PL82613B1 (en)
RO (1) RO62862A (en)
SU (1) SU530639A3 (en)
YU (1) YU36158B (en)
ZA (1) ZA73949B (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1149819A (en) * 1970-01-08 1983-07-12 Max Wilhelm Process for the manufacture of new amines

Also Published As

Publication number Publication date
AU5205273A (en) 1974-08-15
DD105214A1 (en) 1974-04-12
FI59582B (en) 1981-05-29
FI59582C (en) 1981-09-10
LU66869A1 (en) 1973-03-19
JPS5626654B2 (en) 1981-06-19
CS168625B2 (en) 1976-06-29
DK136185C (en) 1978-02-13
DE2264182A1 (en) 1973-12-20
IE37271B1 (en) 1977-06-08
NL7300688A (en) 1973-08-30
ZA73949B (en) 1973-11-28
AT321315B (en) 1975-03-25
YU26073A (en) 1981-06-30
DE2264182B2 (en) 1981-06-25
DE2264182C3 (en) 1982-03-18
JPS4897838A (en) 1973-12-13
YU36158B (en) 1982-02-25
HU165235B (en) 1974-07-27
PL82613B1 (en) 1975-10-31
CH577956A5 (en) 1976-07-30
SU530639A3 (en) 1976-09-30
FR2173990B1 (en) 1976-09-03
IE37271L (en) 1973-08-28
RO62862A (en) 1978-02-15
BE796029A (en) 1973-08-27
DK136185B (en) 1977-08-29
FR2173990A1 (en) 1973-10-12
GB1397663A (en) 1975-06-18

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Legal Events

Date Code Title Description
FD1A Patent lapsed

Effective date: 19840409