GB1495422A - 3-(4-(2-alkoxy cabonylamino ethyl)-phenoxy)-1-isopropylamino-propan-2-ols methods for their preparation and compositions containing them - Google Patents

3-(4-(2-alkoxy cabonylamino ethyl)-phenoxy)-1-isopropylamino-propan-2-ols methods for their preparation and compositions containing them

Info

Publication number
GB1495422A
GB1495422A GB3684/75A GB368475A GB1495422A GB 1495422 A GB1495422 A GB 1495422A GB 3684/75 A GB3684/75 A GB 3684/75A GB 368475 A GB368475 A GB 368475A GB 1495422 A GB1495422 A GB 1495422A
Authority
GB
United Kingdom
Prior art keywords
formula
compound
ethyl
image
cabonylamino
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
GB3684/75A
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 GB1495422A publication Critical patent/GB1495422A/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
    • C07D303/24Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/16Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by singly-bound oxygen atoms

Landscapes

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

Abstract

Novel amines of the formula (I) <IMAGE> in which R denotes methyl or ethyl, are prepared by an N-alkylation process. This starts either from a compound of the formula (II) <IMAGE> wherein X<1> denotes the hydroxyl group and Z a reactive esterified hydroxyl group or X<1> and Z together form an epoxy group, which compound is reacted with isopropylamine, or starts from a compound of the formula (III) <IMAGE> wherein R has the above meaning, which is reacted with a compound of the formula (IV> Z-CH=(CH3)2 (IV> wherein Z has the abovementioned meaning. The amines are obtained in the form of free bases or of therapeutically acceptable acid addition salts. The compounds of the formula (I) possess valuable pharmacological properties; they exhibit, for example, cardioselective ss-receptorblocking properties whilst retaining activities which are useful in the treatment of Angina pectoris.
GB3684/75A 1974-01-29 1975-01-28 3-(4-(2-alkoxy cabonylamino ethyl)-phenoxy)-1-isopropylamino-propan-2-ols methods for their preparation and compositions containing them Expired GB1495422A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE7401096A SE419754B (en) 1974-01-29 1974-01-29 ANALOGY PROCEDURE FOR PREPARING TWO NEW SUBSTITUTED PHENOXYPROPANOLAMINES WITH ALFA RECEPTOR BLOCKING EFFECT

Publications (1)

Publication Number Publication Date
GB1495422A true GB1495422A (en) 1977-12-21

Family

ID=20320031

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3684/75A Expired GB1495422A (en) 1974-01-29 1975-01-28 3-(4-(2-alkoxy cabonylamino ethyl)-phenoxy)-1-isopropylamino-propan-2-ols methods for their preparation and compositions containing them

Country Status (22)

Country Link
JP (1) JPS50106930A (en)
AT (1) AT336037B (en)
BE (1) BE824900A (en)
CA (1) CA1048526A (en)
CH (1) CH614933A5 (en)
CS (3) CS185700B2 (en)
DD (1) DD119222A5 (en)
DE (1) DE2500249A1 (en)
DK (1) DK137122B (en)
FI (1) FI750053A (en)
FR (1) FR2258850A1 (en)
GB (1) GB1495422A (en)
HK (1) HK66980A (en)
HU (1) HU168520B (en)
IE (1) IE41131B1 (en)
LU (1) LU71746A1 (en)
MY (1) MY8100207A (en)
NL (1) NL7501044A (en)
NO (1) NO750098L (en)
SE (1) SE419754B (en)
SU (3) SU550977A3 (en)
ZA (1) ZA748195B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0330180U (en) * 1989-07-31 1991-03-25

Also Published As

Publication number Publication date
SU622395A3 (en) 1978-08-30
DK137122B (en) 1978-01-23
SU584761A3 (en) 1977-12-15
CS185700B2 (en) 1978-10-31
JPS50106930A (en) 1975-08-22
DK24375A (en) 1975-10-06
AT336037B (en) 1977-04-12
CS185673B2 (en) 1978-10-31
LU71746A1 (en) 1975-12-09
BE824900A (en) 1975-07-29
DE2500249A1 (en) 1975-07-31
ATA61675A (en) 1976-08-15
ZA748195B (en) 1976-01-28
HU168520B (en) 1976-05-28
SE7401096L (en) 1975-07-30
MY8100207A (en) 1981-12-31
SU550977A3 (en) 1977-03-15
DD119222A5 (en) 1976-04-12
IE41131L (en) 1975-07-29
IE41131B1 (en) 1979-10-24
FR2258850A1 (en) 1975-08-22
HK66980A (en) 1980-12-05
CH614933A5 (en) 1979-12-28
FI750053A (en) 1975-07-30
SE419754B (en) 1981-08-24
DK137122C (en) 1978-06-26
NL7501044A (en) 1975-07-31
CA1048526A (en) 1979-02-13
NO750098L (en) 1975-08-25
FR2258850B1 (en) 1980-02-08
CS185699B2 (en) 1978-10-31
AU7764675A (en) 1976-07-29

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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