CH240400A - Process for the preparation of an acylated, aliphatic aminocarboxamide. - Google Patents
Process for the preparation of an acylated, aliphatic aminocarboxamide.Info
- Publication number
- CH240400A CH240400A CH240400DA CH240400A CH 240400 A CH240400 A CH 240400A CH 240400D A CH240400D A CH 240400DA CH 240400 A CH240400 A CH 240400A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- acylated
- preparation
- aliphatic
- aminocarboxamide
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zier Darstellung eines acylierten, aliphatisehen Aminocarbonsäureaniids. Gegenstand des vorliegenden Zusatz patentes ist ein Verfahren zur Darstellung eines acylierten, aliphatischen Aminocarbon- säureamids.Das Verfahren ist dadurch gekenn zeichnet, dass ein a-Halogen-n-buttersäure- methyläthylamid mit Äthylamin umgesetzt und das Reaktionsprodukt mit einer das Ra dikal der ss,
ss-Dimethyl-acrylsäure abgeben den Verbindung acyliert wird.
Das N-(l,ss-Dimethyl - acroyl) -a-äthyl- amino - n - buttersäuremethyläthylamid der Formel
EMI0001.0021
bildet eine farblose Flüssigkeit vom Siede punkt 125-l26 unter 0,1 mm.
Die neue Verbindung soll therapeutische Verwendung finden. <I>Beispiel:</I> 3'4,2 Teile a-Äthylamino-n-buttersäure- methyläthylamid, Kp13 106-109 (darge stellt aus a-Brom-n-buttersäuremethyläthyl- amid durch Erhitzen mit Äthylamin),
wer den in 200 Teilen Äther gelöst und unter Rühren und Kühlen 12 Teile f'"8-Dimethyl- acrylsäurechlorid zugetropft. Nach 2stündi- gem Rühren wird vom a-Äthylamino-n- buttersäuremethyläthylamid-chlorhydrat erb- filtriert und die ätherische Lösung mit ge sättigter Kalilauge geschüttelt. Nach dem Abdestillieren des Lösungsmittels wird das Reaktionsprodukt im Hochvakuum rektifi ziert.
Die neue Verbindung siedet bei 125 bis 126 unter 0,1 mm und ist leicht löslich in Wasser und organischen Lösungsmitteln.
Process for the preparation of an acylated, aliphatic aminocarboxylic acid aniide. The subject of the present additional patent is a process for the preparation of an acylated, aliphatic aminocarboxylic acid amide. The process is characterized in that an α-halo-n-butyric acid methylethylamide is reacted with ethylamine and the reaction product is
ss-dimethyl acrylic acid release the compound is acylated.
The N- (l, ss-dimethyl-acroyl) -a-ethyl-amino-n-butyric acid methylethylamide of the formula
EMI0001.0021
forms a colorless liquid with a boiling point of 125-126 below 0.1 mm.
The new compound should find therapeutic use. <I> Example: </I> 3'4.2 parts of a-ethylamino-n-butyric acid methylethylamide, Kp13 106-109 (shown from a-bromo-n-butyric acid methylethylamide by heating with ethylamine),
are dissolved in 200 parts of ether and 12 parts of 8-dimethyl acrylic acid chloride are added dropwise with stirring and cooling After the solvent has been distilled off, the reaction product is rectified in a high vacuum.
The new compound boils below 0.1 mm at 125 to 126 mm and is easily soluble in water and organic solvents.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH234453T | 1942-12-18 | ||
| CH240400T | 1942-12-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH240400A true CH240400A (en) | 1945-12-15 |
Family
ID=25727917
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH240400D CH240400A (en) | 1942-12-18 | 1942-12-18 | Process for the preparation of an acylated, aliphatic aminocarboxamide. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH240400A (en) |
-
1942
- 1942-12-18 CH CH240400D patent/CH240400A/en unknown
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