GB995747A - Improvements in or relating to amine derivatives of 1,5-diazacyclooctane - Google Patents
Improvements in or relating to amine derivatives of 1,5-diazacyclooctaneInfo
- Publication number
- GB995747A GB995747A GB39667/61A GB3966761A GB995747A GB 995747 A GB995747 A GB 995747A GB 39667/61 A GB39667/61 A GB 39667/61A GB 3966761 A GB3966761 A GB 3966761A GB 995747 A GB995747 A GB 995747A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- diazacyclooctane
- diazabicyclo
- amine derivatives
- compound
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/08—Bridged systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
The invention comprises amine derivatives of 1,5-diazacyclooctane of formula <FORM:0995747/C2/1> where n is from 2 to 12, and their acid addition salts. The compounds are prepared by reducing a compound of formula <FORM:0995747/C2/2> where Z is a nitrile or carbamyl radical. The compounds of formula IV are prepared by reacting a 1,5-diazabicyclo-(3,3,1)-nonaneonium derivative of formula <FORM:0995747/C2/3> where Hal is chlorine, bromine or iodine, with an alkali metal cyanide. The compound III may be produced by condensing 1,5-diazabicyclo-(3,3,1)-nonane with a compound of formula Hal-(CH2)n- 1-Z The 1,5-diazabicyclo-(3,3,1)-nonane may be obtained by reacting 1,5-diazacyclooctane with formaldehyde. Examples are given.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH1288760A CH405330A (en) | 1960-11-17 | 1960-11-17 | Process for the preparation of new heterocyclic compounds |
CH24461 | 1961-01-10 | ||
CH1078761 | 1961-09-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB995747A true GB995747A (en) | 1965-06-23 |
Family
ID=27171936
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB39667/61A Expired GB995747A (en) | 1960-11-17 | 1961-11-06 | Improvements in or relating to amine derivatives of 1,5-diazacyclooctane |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB995747A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5348561A (en) * | 1990-03-01 | 1994-09-20 | Exxon Chemical Patents Inc. | Fuel oil compositions |
-
1961
- 1961-11-06 GB GB39667/61A patent/GB995747A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5348561A (en) * | 1990-03-01 | 1994-09-20 | Exxon Chemical Patents Inc. | Fuel oil compositions |
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