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GB1524036A - Amines - Google Patents

Amines

Info

Publication number
GB1524036A
GB1524036A GB37073/75A GB3707375A GB1524036A GB 1524036 A GB1524036 A GB 1524036A GB 37073/75 A GB37073/75 A GB 37073/75A GB 3707375 A GB3707375 A GB 3707375A GB 1524036 A GB1524036 A GB 1524036A
Authority
GB
United Kingdom
Prior art keywords
propan
ethylamino
carbamylphenoxy
allylphenoxy
methyl
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
GB37073/75A
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.)
Hassle AB
Original Assignee
Hassle AB
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 Hassle AB filed Critical Hassle AB
Publication of GB1524036A publication Critical patent/GB1524036A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D277/00Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three 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
    • C07D277/34Oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pulmonology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Thiazole And Isothizaole Compounds (AREA)

Abstract

For the preparation of novel hydroxyamines of the formula (I) <IMAGE> with the radicals as in Patent Claim 1, and of therapeutically acceptable acid addition salts of these compounds, a starting compound of the formula (II) <IMAGE> is used. This is reacted with an amine of the formula (III) <IMAGE> The resulting isomeric mixtures are separated into the pure isomers and the resulting racemates into the optical antipodes. The resulting free bases can be converted into their salts and the resulting salts converted into the corresponding free bases. Preferred compounds prepared are: 1) 1-[2-(4-carbamylphenoxy)ethylamino]-3-(2-allylphenoxy)propan-2-ol, 2) 1-[2-(4-carbamylphenoxy)ethylamino]-3-(2-methoxyethyl)phenoxy-propan-2 -ol, 3) 1-[1-methyl-2-(4-carbamylphenoxy)ethylamino]-3-(2-allyl-phenoxy)propan -2-ol, 4) 1-[1-methyl-2-(2-methylphenoxy)ethylamino]-3-(2-allylphenoxy)-propan-2 -ol, 5) 1-[1-methyl-2-(4-methylphenoxy)ethylamino]-3-(2-allylphenoxy)-propan-2 -ol, 6) 1-[1-methyl-2-(4-carbamylphenoxy)ethylamino]-3-(2-methylisonitrosometh ylphenoxy)propan-2-ol, 7) 1-[2-(4-carbamylphenoxy)ethylamino]-3-(3-allylphenoxy)-propan-2-ol. The compounds have a blocking effect on beta -receptors and can be employed for the treatment of cardiovascular disorders.
GB37073/75A 1974-11-01 1975-09-09 Amines Expired GB1524036A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE7413789A SE422052B (en) 1974-11-01 1974-11-01 PROCEDURE FOR PREPARING CERTAIN STATED 1-PHENOXY-2-HYDROXY-3-AMINOPHENYL PROPYL DERIVATIVES

Publications (1)

Publication Number Publication Date
GB1524036A true GB1524036A (en) 1978-09-06

Family

ID=20322597

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37073/75A Expired GB1524036A (en) 1974-11-01 1975-09-09 Amines

Country Status (24)

Country Link
JP (1) JPS51131839A (en)
AT (1) AT344142B (en)
AU (1) AU498770B2 (en)
BE (2) BE835090A (en)
CA (1) CA1093095A (en)
CH (3) CH618417A5 (en)
CS (1) CS189726B2 (en)
DD (1) DD119207A5 (en)
DE (1) DE2531312A1 (en)
DK (1) DK444475A (en)
FI (1) FI752201A (en)
FR (1) FR2289172A1 (en)
GB (1) GB1524036A (en)
HK (1) HK36081A (en)
HU (1) HU172652B (en)
IE (1) IE41652B1 (en)
LU (1) LU73703A1 (en)
MY (1) MY8200085A (en)
NL (1) NL7509548A (en)
NO (1) NO144773C (en)
NZ (1) NZ178313A (en)
SE (1) SE422052B (en)
SU (3) SU906368A3 (en)
ZA (2) ZA754241B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5001161A (en) * 1984-01-10 1991-03-19 Aktiebolaget Hassle Pharmaceutical composition comprising metroprolol succinate

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4119718A (en) * 1977-05-02 1978-10-10 Merck & Co., Inc. 3-Amino-2-oxy-propoxy-substituted isothiazoles
SE7807408L (en) * 1978-06-30 1979-12-31 Haessle Ab HEART ACTIVE ASSOCIATIONS
DD150456A5 (en) * 1979-03-01 1981-09-02 Ciba Geigy Ag PROCESS FOR THE PREPARATION OF DERIVATIVES OF 3-AMINO-1,2-PROPANDIOL
DE3125870C2 (en) * 1980-07-09 1994-09-15 William John Louis 3-aminopropoxyphenyl derivatives, their preparation and medicaments containing them
US4410548A (en) * 1980-07-09 1983-10-18 Reckitt & Colman Products Limited Propanolamine derivatives
FR2508032A1 (en) * 1981-06-17 1982-12-24 Delalande Sa 3-Amino-2-aryloxy-methyl-1-propanol derivs. - are used to treat cardiovascular troubles, esp. angina esp 3-tri:methoxy-cinnamoyl-piperazino- 2-1,4-benzodioxan-5-yl-oxy-methyl cpds.
DE3151201A1 (en) * 1981-12-23 1983-07-28 Beiersdorf Ag, 2000 Hamburg SUBSTITUTED PHENOXYALKANOLAMINE AND PHENOXYALKANOL-CYCLOALKYLAMINE, METHOD FOR THE PRODUCTION THEREOF, PHARMACEUTICAL PREPARATIONS CONTAINING THESE COMPOUNDS AND INTERMEDIATE PRODUCTS
DE3433616A1 (en) * 1984-08-08 1986-02-20 BBC Aktiengesellschaft Brown, Boveri & Cie., Baden, Aargau PROTECTIVE DEVICE FOR AN ELECTRICAL NET
JPS6341451A (en) * 1986-08-06 1988-02-22 Nippon Kayaku Co Ltd Ether derivative and miticidal and insecticidal composition containing said derivative as active component
US5321036A (en) * 1993-02-10 1994-06-14 Bristol-Myers Squibb Company Thiazole and oxazole-based β3 adrenergic receptor agonists

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5001161A (en) * 1984-01-10 1991-03-19 Aktiebolaget Hassle Pharmaceutical composition comprising metroprolol succinate

Also Published As

Publication number Publication date
ZA754240B (en) 1976-06-30
CA1093095A (en) 1981-01-06
HK36081A (en) 1981-07-31
BE835091A (en) 1976-04-30
CS189726B2 (en) 1979-04-30
ZA754241B (en) 1976-06-30
SE7413789L (en) 1976-05-03
CH622491A5 (en) 1981-04-15
JPS51131839A (en) 1976-11-16
IE41652B1 (en) 1980-02-27
NL7509548A (en) 1976-05-04
ATA592975A (en) 1977-11-15
SU906368A3 (en) 1982-02-15
NZ178313A (en) 1978-06-02
CH622490A5 (en) 1981-04-15
NO144773C (en) 1981-11-04
NO144773B (en) 1981-07-27
SU637078A3 (en) 1978-12-05
MY8200085A (en) 1982-12-31
FI752201A (en) 1976-05-02
SE422052B (en) 1982-02-15
NO752765L (en) 1976-05-04
IE41652L (en) 1976-05-01
DD119207A5 (en) 1976-04-12
FR2289172A1 (en) 1976-05-28
LU73703A1 (en) 1976-08-13
AU8363775A (en) 1977-02-10
HU172652B (en) 1977-11-28
DK444475A (en) 1976-05-02
CH618417A5 (en) 1980-07-31
AU498770B2 (en) 1979-03-22
BE835090A (en) 1976-04-30
FR2289172B1 (en) 1980-11-21
DE2531312A1 (en) 1976-05-06
SU625599A3 (en) 1978-09-25
AT344142B (en) 1978-07-10

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee