GB849032A - Improvements in and relating to azepine derivatives - Google Patents

Improvements in and relating to azepine derivatives

Info

Publication number
GB849032A
GB849032A GB20125/58A GB2012558A GB849032A GB 849032 A GB849032 A GB 849032A GB 20125/58 A GB20125/58 A GB 20125/58A GB 2012558 A GB2012558 A GB 2012558A GB 849032 A GB849032 A GB 849032A
Authority
GB
United Kingdom
Prior art keywords
formula
iminostilbenes
reacting
represent
products
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
GB20125/58A
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 GB849032A publication Critical patent/GB849032A/en
Expired legal-status Critical Current

Links

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

The invention comprises compounds of the general formulae: <FORM:0849032/IV(b)/1> and <FORM:0849032/IV(b)/2> and the acid addition salts of I, wherein X1 and X2 represent hydrogen or halogen atoms, R1 and R2 represent alkyl or alkenyl groups containing 1 to 5 carbon atoms or R1 and R2 together with the nitrogen atom represent an alkylene imino radical having 5 or 6 ring members or the morpholino radical, R3 represents an alkyl or alkenyl group containing 1 to 6 carbon atoms or an araliphatic group, Y represents a monovalent anion or a normal equivalent of a polyvalent anion, and n is a whole number from 1 to 5; and the preparation of I by reacting a possibly ring substituted N-halogenoalkanoyliminostilbene of the general formula: <FORM:0849032/IV(b)/3> in which Hal represents chlorine or bromine, with an excess of an amine HNR1R2; and, if desired, converting the products into their acid addition salts; and the preparation of II by treatment of I with a reactive ester of an alcohol R3OH followed, if desired, by exchange of anions of II. The products of formula I have local anaesthetic activity and those of formula II have spasmolytic properties. N-Halogenoalkanoyl-iminostilbenes, are prepared by reacting iminostilbenes with halogenocarboxylic acid halides. Specification 820,476 is referred to.
GB20125/58A 1957-06-25 1958-06-24 Improvements in and relating to azepine derivatives Expired GB849032A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH849032X 1957-06-25

Publications (1)

Publication Number Publication Date
GB849032A true GB849032A (en) 1960-09-21

Family

ID=4542112

Family Applications (1)

Application Number Title Priority Date Filing Date
GB20125/58A Expired GB849032A (en) 1957-06-25 1958-06-24 Improvements in and relating to azepine derivatives

Country Status (4)

Country Link
CH (2) CH358806A (en)
DE (1) DE1124501B (en)
GB (1) GB849032A (en)
NL (1) NL106266C (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE456311A (en) * 1951-07-11

Also Published As

Publication number Publication date
DE1124501B (en) 1962-03-01
CH358805A (en) 1961-12-15
CH358806A (en) 1961-12-15
NL106266C (en)

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