GB1513110A - Therapeutically active phenylethanolamine derivatives - Google Patents

Therapeutically active phenylethanolamine derivatives

Info

Publication number
GB1513110A
GB1513110A GB43348/76A GB4334876A GB1513110A GB 1513110 A GB1513110 A GB 1513110A GB 43348/76 A GB43348/76 A GB 43348/76A GB 4334876 A GB4334876 A GB 4334876A GB 1513110 A GB1513110 A GB 1513110A
Authority
GB
United Kingdom
Prior art keywords
formula
benzyl
compounds
oct
salts
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
GB43348/76A
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.)
Bruneau & Cie Lab
Original Assignee
Bruneau & Cie Lab
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 Bruneau & Cie Lab filed Critical Bruneau & Cie Lab
Publication of GB1513110A publication Critical patent/GB1513110A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/58Radicals substituted by nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/54Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C217/56Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
    • C07C217/62Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/673Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/70Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
    • C07C45/71Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Abstract

1513110 Phenylalkanoylamines LES LABORATOIRES BRUNEAU & CIE 19 Oct 1976 [22 Oct 1975] 43348/76 Heading C2C Compounds of the general Formula (I) (Z = C 2-4 hydroxyalkyl, C 3-4 dihydroxyalkyl; R = H, C 1-6 alkyl; R 1 = H, C 1-6 alkyl, C 3-6 cycloalkyl, R 2 R 3 R 4 PhC x H 2x ; x = 2-5; R 2-4 = H, OH, OMe, OEt or two in adjacent positions = O(CH 2 ) 1 , 2 O) and their salts and N- benzyl and dibenzyl (R 1 = H) derivatives are prepared by brominating a compound of the Formula (II) (Z<SP>1</SP> = acylated Z; Ac = acyl, benzyl), condensing the α-bromoketone obtained with the appropriate primary amine or its benzyl derivative or dibenzylamine, in any order removing the protecting groups and reducing the CO group to CHOH, if desired reductively alkylating a resulting primary amine, effecting isomer separation and/or converting the product to a salt. The preparation of the starting materials of Formula (II), the corresponding compounds in which the phenolic hydroxy group and/or the hydroxy group(s) in the side chain are not protected o - (2 - acetoxyethoxy)phenyl acetate and o - (2 - propionoxyethoxy)phenyl propionate is described. The compounds of Formula (I) and their salts are bronchospasmolytics, and may be administered in the form of pharmaceutical preparations containing them in association with a carrier.
GB43348/76A 1975-10-22 1976-10-19 Therapeutically active phenylethanolamine derivatives Expired GB1513110A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7532286A FR2328456A1 (en) 1975-10-22 1975-10-22 PHENYLETHANOLAMINE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION

Publications (1)

Publication Number Publication Date
GB1513110A true GB1513110A (en) 1978-06-07

Family

ID=9161500

Family Applications (1)

Application Number Title Priority Date Filing Date
GB43348/76A Expired GB1513110A (en) 1975-10-22 1976-10-19 Therapeutically active phenylethanolamine derivatives

Country Status (3)

Country Link
DE (1) DE2647866A1 (en)
FR (1) FR2328456A1 (en)
GB (1) GB1513110A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0052963A1 (en) * 1980-11-20 1982-06-02 Beecham Group Plc Secondary amines

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5108363A (en) * 1988-02-19 1992-04-28 Gensia Pharmaceuticals, Inc. Diagnosis, evaluation and treatment of coronary artery disease by exercise simulation using closed loop drug delivery of an exercise simulating agent beta agonist

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0052963A1 (en) * 1980-11-20 1982-06-02 Beecham Group Plc Secondary amines
US4382958A (en) 1980-11-20 1983-05-10 Beecham Group Limited Secondary amines and compositions for treatment of hypoglycaemia or obesity

Also Published As

Publication number Publication date
DE2647866A1 (en) 1977-05-05
FR2328456B1 (en) 1978-11-10
FR2328456A1 (en) 1977-05-20

Similar Documents

Publication Publication Date Title
AU539976B2 (en) Therapeutically active compounds
GB1204195A (en) Phenylalkanolamine derivatives
GB1480772A (en) Antibiotic derivatives
GB1438265A (en)
ES8504682A1 (en) New nitro aliphatic compounds, process for preparation thereof and use thereof.
GB1396726A (en) Phenylalkanoic acids
GB1513110A (en) Therapeutically active phenylethanolamine derivatives
ES8701143A1 (en) 2-Hydroxy-3-aryloxypropyl or 2-hydroxy-2-benzofuranyl ethyl tertiary amine having an anti-hyperglycaemic and/or anti-obesity activity.
GB1523598A (en) Tripeptides
GB1449799A (en) A-aminoalkyl-substituted-benzyl alcohols
GB1354216A (en) Substituted isoquinolines and a process for the preparation thereof
SE7408868L (en)
JPS5219684A (en) Preparation of novel alpha-amino acid derivatives
GB1265117A (en)
GB1466553A (en) Salts of a penicillanic acid derivative
GB1367678A (en) Substituted phenyl aminoethanols
GB1421685A (en) Phenoxyalkanecarboxylic acid derivative the preparation thereof and pharmaceutical compositions containing it
IE32514B1 (en) Synthesis of adamantyl compounds
JPS5227748A (en) Preparation of novel prostaglandin derivatives
JPS5444681A (en) 5-fluororacil derivative
GB1511179A (en) Pharmaceutical compositions

Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee