GB929788A - Azepine derivatives and processes for producing same - Google Patents

Azepine derivatives and processes for producing same

Info

Publication number
GB929788A
GB929788A GB2104659A GB2104659A GB929788A GB 929788 A GB929788 A GB 929788A GB 2104659 A GB2104659 A GB 2104659A GB 2104659 A GB2104659 A GB 2104659A GB 929788 A GB929788 A GB 929788A
Authority
GB
United Kingdom
Prior art keywords
salts
inorganic
compounds
general formula
organic acids
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
GB2104659A
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.)
Novartis AG
Original Assignee
JR Geigy 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 JR Geigy AG filed Critical JR Geigy AG
Publication of GB929788A publication Critical patent/GB929788A/en
Expired legal-status Critical Current

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

The invention comprises: (a) compounds of the general formula <FORM:0929788/IV(a)/1> (wherein X represents -CH2-CH2- or -CH=CH-, Y and Z represent hydrogen or halogen atoms or methyl or ethyl groups, and represents a hydrogen atom or an alkyl or aralkyl radical) and their salts with inorganic and organic acids; (b) the preparation thereof by reduction or hydrogenation (the latter preferably in the presence of ammonia) of compounds of the general formula <FORM:0929788/IV(a)/2> followed, if desired, by conversion of the products into salts with inorganic or organic acids; and (c) the combination of process (b) with the preparation of the starting materials by the process of Specification 929,789. The products may be dialkylated at the primary amino group, and both the primary and the tertiary amines have pharmaceutical uses (see Group VI).ALSO:Compounds of the general formula <FORM:0929788/VI/1> (wherein X represents -CH2-CH2- or -CH =CH-, Y and Z represent hydrogen or halogen atoms or methyl or ethyl groups, and R represents a hydrogen atom or an alkyl or aralkyl radical), and their salts with inorganic and organic acids, are useful as cholinesterase inhibitors, antiallergics, antipyretics, serotonin antagonists, and potentiators of analgesics and anaesthetics. The tertiary amines derived therefrom by dialkylation are useful for similar purposes and also as sedatives. Specification 929,789 is referred to.
GB2104659A 1958-06-24 1959-06-19 Azepine derivatives and processes for producing same Expired GB929788A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH6095458A CH368495A (en) 1958-06-24 1958-06-24 Process for the production of azepine derivatives

Publications (1)

Publication Number Publication Date
GB929788A true GB929788A (en) 1963-06-26

Family

ID=4523304

Family Applications (2)

Application Number Title Priority Date Filing Date
GB966463A Expired GB929789A (en) 1958-06-24 1959-06-19 Azepine derivatives and processes for producing same
GB2104659A Expired GB929788A (en) 1958-06-24 1959-06-19 Azepine derivatives and processes for producing same

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB966463A Expired GB929789A (en) 1958-06-24 1959-06-19 Azepine derivatives and processes for producing same

Country Status (2)

Country Link
CH (1) CH368495A (en)
GB (2) GB929789A (en)

Also Published As

Publication number Publication date
CH368495A (en) 1963-04-15
GB929789A (en) 1963-06-26

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