GB971917A - New aminoindanes and a process for their manufacture - Google Patents

New aminoindanes and a process for their manufacture

Info

Publication number
GB971917A
GB971917A GB3776961A GB3776961A GB971917A GB 971917 A GB971917 A GB 971917A GB 3776961 A GB3776961 A GB 3776961A GB 3776961 A GB3776961 A GB 3776961A GB 971917 A GB971917 A GB 971917A
Authority
GB
United Kingdom
Prior art keywords
hydrogen
compounds
hydroxyl
salts
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
GB3776961A
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.)
Bayer Pharma AG
Original Assignee
Schering 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 Schering AG filed Critical Schering AG
Publication of GB971917A publication Critical patent/GB971917A/en
Expired legal-status Critical Current

Links

Abstract

The invention comprises aminoindanes of formula <FORM:0971917/C1/1> where R1 is hydrogen or acyl, R2 is hydrogen, free hydroxyl or esterified hydroxyl, n is 0 or 1 and Am is an amino group disubstituted by alkyl groups which may themselves be substituted by hydroxyl groups or the amino group may form part of a heterocyclic ring. The compounds are prepared from compounds of formula <FORM:0971917/C1/2> where X is an alkyl, aryl or aralkyl radical and Y is hydrogen, which are reacted, e.g. by boiling with mineral acids, heating with pyridine hydrochloride or by catalytic hydrogenolysis, to replace X by hydrogen and Y, when it is not hydrogen, by hydroxyl. The phenolic hydroxyl groups may be esterified with monocarboxylic acids. Salts may be formed with bases and with compounds having free phenolic OH groups; salts also may be formed with the nitrogen atom of the amino group and acids. Examples are given. The compounds of Formula I produce spasmolytic effects upon the gastrointestinal tract and have local anaesthetic effects. The compounds, or their salts may be used as solutions and may be mixed with sodium dexamethasone sulphate or with basic theophyllin preparations.
GB3776961A 1960-11-08 1961-10-20 New aminoindanes and a process for their manufacture Expired GB971917A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DESC028740 1960-11-08

Publications (1)

Publication Number Publication Date
GB971917A true GB971917A (en) 1964-10-07

Family

ID=7431202

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3776961A Expired GB971917A (en) 1960-11-08 1961-10-20 New aminoindanes and a process for their manufacture

Country Status (1)

Country Link
GB (1) GB971917A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0076669A1 (en) * 1981-10-05 1983-04-13 Kefalas A/S Novel 3-phenyl-1-indanamines, pharmaceutical compositions and methods of preparation

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0076669A1 (en) * 1981-10-05 1983-04-13 Kefalas A/S Novel 3-phenyl-1-indanamines, pharmaceutical compositions and methods of preparation

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