CH298028A - Process for the preparation of a bis-aminoalkoxy-alkane. - Google Patents
Process for the preparation of a bis-aminoalkoxy-alkane.Info
- Publication number
- CH298028A CH298028A CH298028DA CH298028A CH 298028 A CH298028 A CH 298028A CH 298028D A CH298028D A CH 298028DA CH 298028 A CH298028 A CH 298028A
- Authority
- CH
- Switzerland
- Prior art keywords
- bis
- alkane
- preparation
- ethoxy
- aminoalkoxy
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/084—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/088—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Hydrogenated Pyridines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Herstellung eines Bis-aminoalkoxy-alkans. Gegenstand vorliegenden Patentes ist ein Verfahren zur Herstellung eines Bis-amino- alkoxy-alkans. Das Verfahren ist dadurch ge kennzeichnet, dass man ein Mol eines 1,10-Bis- (r9-lialogen-äthoxy)-dekans mit zwei Mol Pi- peridin umsetzt.
Die erhaltene neue Verbindung, das 1,10- Bis-(@-piperidino-äthoxy)-dekan, siedet unter 0,01 mm Druck bei 197-203 . Sie soll als Zwischenprodukt zur Herstellung von Arznei initteln Verwendung finden.
Beispiel: 9,7 Teile 1,10-Bis-(@-brom-äthoxy)-dekan werden in Portionen in 11 TeileIPiperidin einge tragen, wobei sich unter Erwärmung die Um setzung vollzieht. Hierauf. erwärmt man noch 6 Stunden unter Rückfluss, darauf zur Entfer nung des überschüssigen Piperidins einige Zeit im Vakuum. Nach dem Erkalten löst man den Rückstand in verdünnter Salzsäure, schüttelt die salzsaure Lösung zur Entfernung allfälliger Neutralteile mit Äther, klärt sie mit Tierkohle, filtriert und stellt mit 30 /oiger Natronlauge stark alkalisch.
Die ausgeschiedene Base wird in Äther aufgenommen, die ätherische Lösung mit Kaliumhydroxyd getrocknet, der Äther ab gedampft und der Rückstand im Vakuum destil liert. Das 1,10-Bis-(@-piperidino-äthoxy)-dekan siedet unter 0,01 mm Druck bei 197-203 .
Process for the preparation of a bis-aminoalkoxy-alkane. The present patent is a process for the preparation of a bis-amino-alkoxy-alkane. The process is characterized in that one mole of a 1,10-bis- (r9-lialogenoethoxy) decane is reacted with two moles of piperidine.
The new compound obtained, the 1,10-bis- (@ - piperidino-ethoxy) -dekan, boils under 0.01 mm pressure at 197-203. It should be used as an intermediate product in the manufacture of pharmaceuticals.
Example: 9.7 parts of 1,10-bis- (@ -bromo-ethoxy) -dekan are added in portions to 11 parts of IPiperidine, and the reaction takes place when heated. On that. it is heated under reflux for a further 6 hours, then for some time in vacuo to remove the excess piperidine. After cooling, the residue is dissolved in dilute hydrochloric acid, the hydrochloric acid solution is shaken with ether to remove any neutral parts, clarified with animal charcoal, filtered and made strongly alkaline with 30% sodium hydroxide solution.
The precipitated base is taken up in ether, the ethereal solution is dried with potassium hydroxide, the ether is evaporated and the residue is distilled in vacuo. The 1,10-bis- (@ - piperidino-ethoxy) -dekan boils under 0.01 mm pressure at 197-203.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH292945T | 1951-09-20 | ||
CH298028T | 1951-09-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH298028A true CH298028A (en) | 1954-04-15 |
Family
ID=25733310
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH298028D CH298028A (en) | 1951-09-20 | 1951-09-20 | Process for the preparation of a bis-aminoalkoxy-alkane. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH298028A (en) |
-
1951
- 1951-09-20 CH CH298028D patent/CH298028A/en unknown
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CH298028A (en) | Process for the preparation of a bis-aminoalkoxy-alkane. | |
CH298030A (en) | Process for the preparation of a bis-aminoalkoxy-alkane. | |
DE826133C (en) | Process for the preparation of dihydroresorcinol carbamic acid esters | |
DE832892C (en) | Process for the preparation of condensation products of rutin | |
DE726431C (en) | Process for the preparation of arylides from ª ‰ -ketone carboxylic acids | |
DE646932C (en) | Process for the production of diamino alcohols of the fatty aromatic series | |
CH298785A (en) | Process for the preparation of a diquartar diammonium salt. | |
CH104927A (en) | Process for the production of a thionaphthisatin. | |
CH232058A (en) | Process for the preparation of 1-phenyl-2-dimethylaminopropanol- (1). | |
CH281966A (en) | Process for the preparation of a heterocyclic carbamic acid derivative. | |
CH204700A (en) | Process for the production of a condensation product. | |
CH204120A (en) | Process for the production of a perinaphthindanedione sulfonic acid. | |
CH149006A (en) | Process for the preparation of a halogen-containing basic ether. | |
CH308813A (en) | Process for the preparation of an ammonium compound. | |
CH217132A (en) | Process for the production of a water-soluble, higher molecular weight, α-substituted benzylamine derivative. | |
CH200665A (en) | Process for the production of a condensation product. | |
CH281947A (en) | Process for the preparation of a heterocyclic carbamic acid derivative. | |
CH226816A (en) | Process for preparing 5-pregnen-3-ol-20-one. | |
CH140916A (en) | Process for the preparation of 4- (di- (oxyethyl)) - amino-3-methyl-1-oxybenzene. | |
CH110427A (en) | Process for the preparation of an alkamine ester of an aromatic aminocarboxylic acid. | |
CH300759A (en) | Process for producing a phosphoric acid ester. | |
CH245912A (en) | Process for the preparation of an acylated, aliphatic aminocarboxamide. | |
CH121705A (en) | Process for the preparation of a diarylamine. | |
CH104926A (en) | Process for the production of a thionaphthisatin. | |
CH318362A (en) | Process for the preparation of a hydrazone of a heterocyclic aldehyde |