CH161749A - Process for the preparation of 2-dicyclohexylaminoethylaminopyridine. - Google Patents
Process for the preparation of 2-dicyclohexylaminoethylaminopyridine.Info
- Publication number
- CH161749A CH161749A CH161749DA CH161749A CH 161749 A CH161749 A CH 161749A CH 161749D A CH161749D A CH 161749DA CH 161749 A CH161749 A CH 161749A
- Authority
- CH
- Switzerland
- Prior art keywords
- preparation
- dicyclohexylaminoethylaminopyridine
- dibromohydrate
- aminopyridine
- melting point
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
Description
Verfahren zur Darstellung von 2-Dieyeloheaylaminoäthylaminopyridin. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung von 2-Di- cyelohexylaminoäthylaminopyridin, welches darin besteht, dass man Chloräthyldicyclo- hexylamin mit der Natriumverbindung des 2-Aminopyridins umsetzt.
Die neue Verbindung ist als Heilmittel verwendbar und siedet unter 2 mm Druck bei 190-r95 ; sie bildet ein Dibromhydrat vom Schmelzpunkt 198 C.
<I>Beispiel:</I> 20 Gewichtsteile 2-Aminopyridin, 200 Ge wichtsteile Toluol und 8 Gewichtsteile Na- triumamid werden unter Rühren 11/2 Stunden auf dem Dampfbad erwärmt. Danach gibt man 36 Gewichtsteile Ohloräthyldicyclohexyl- amin hinzu und erhitzt weiter eine Stunde auf dem Dampfbad. Nach dem Erkalten ver setzt man mit Wasser, trennt das Toluol ab und reinigt die neue Base:
EMI0001.0018
nach dem Trocknen und Abdestillieren des Toluols im Vakuum.
Sie siedet bei 2 mm Druck bei 190-195 und liefert ein Dibrom- hydrat vom Schmelzpunkt<B>1980</B> C.
Process for the preparation of 2-Dieyeloheaylaminoäthylaminopyridin. The present invention relates to a process for the preparation of 2-dicyelohexylaminoethylaminopyridine, which consists in reacting chloroethyldicyclohexylamine with the sodium compound of 2-aminopyridine.
The new compound is useful as a remedy and boils under 2mm pressure at 190-r95; it forms a dibromohydrate with a melting point of 198 C.
<I> Example: </I> 20 parts by weight of 2-aminopyridine, 200 parts by weight of toluene and 8 parts by weight of sodium amide are heated for 11/2 hours on the steam bath while stirring. Then 36 parts by weight of chloroethyldicyclohexylamine are added and the mixture is heated on the steam bath for a further hour. After cooling down, water is added, the toluene is separated off and the new base is purified:
EMI0001.0018
after drying and distilling off the toluene in vacuo.
It boils at 190-195 at 2 mm pressure and yields a dibromohydrate with a melting point of <B> 1980 </B> C.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH158827T | 1932-07-15 | ||
CH161749T | 1932-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH161749A true CH161749A (en) | 1933-05-15 |
Family
ID=25717152
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH161749D CH161749A (en) | 1932-07-15 | 1932-07-15 | Process for the preparation of 2-dicyclohexylaminoethylaminopyridine. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH161749A (en) |
-
1932
- 1932-07-15 CH CH161749D patent/CH161749A/en unknown
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