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CH311673A - Process for the production of a new basic substituted fatty acid amide. - Google Patents

Process for the production of a new basic substituted fatty acid amide.

Info

Publication number
CH311673A
CH311673A CH311673DA CH311673A CH 311673 A CH311673 A CH 311673A CH 311673D A CH311673D A CH 311673DA CH 311673 A CH311673 A CH 311673A
Authority
CH
Switzerland
Prior art keywords
diethylamine
amide
radical
fatty acid
propyl
Prior art date
Application number
Other languages
German (de)
Inventor
Aktiengesellschaft Cilag
Original Assignee
Cilag 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 Cilag Ag filed Critical Cilag Ag
Publication of CH311673A publication Critical patent/CH311673A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic 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
    • C07D295/04Heterocyclic 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
    • C07D295/14Heterocyclic 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 carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C233/00Carboxylic acid amides
    • C07C233/01Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C233/02Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  



  Verfahren zur Herstellung eines neuen basisch substituierten   Fettsiureamides.   



   Gegenstand des vorliegenden Patentes bildet ein Verfahren zur Herstellung eines neuen basisch substituierten Fettsäureamides, welehes dadurch gekennzeichnet ist, dass man eine Verbindung der Formel
EMI1.1     
 in welcher X einen reaktionsfähigen, während der Reaktion sich abspaltenden Rest bedeutet, mit Diäthylamin umsetzt.



   Der Rest X kann in einem Halogenatom oder einem sonstigen für den Austausch gegen den basischen Rest geeigneten reaktionsfähi  en    Substituenten, wie zum Beispiel einer Alkylsulfonyloxy- oder Arylsulfonyloxygruppe, bestehen. Der Austausch der Gruppe X gegen den Diäthylaminorest erfolgt zum Beispiel durch einfaches Erwärmen mit Diäthylamin, gegebenenfalls in Gegenwart eines basisch reagierenden Kondensationsmittels oder von Diäthylamin im Überschuss. Das   p-Diäthyl-       amino-propionsäure-N-(3-o-aeetamino-phen-      oxy-propyl-2)-meth, ylamid    ist eine farblose zähflüssige Masse. Das   Pikrat    der Base sehmilzt bei   125-126 .   



   Das neue Amid soll als   Lokalanästhetikum    und als Zwischenprodukt zur Herstellung weiterer Derivate Verwendung finden.



   Beispiel :
5, 5 g   S-Brom-propionsäure-N-(3-o-acet-      amino-phenoxy-propyl-2)-methylamid    und 7, 3 g Diäthylamin werden zusammen in 100 em3 abs. Benzol 3 Stunden auf dem Wasserbad erhitzt. Das Reaktionsgemisch wird mit Wasser ausgeschüttelt und dann mit 2n-Salzsäure ausgezogen. Darauf wird der salzsaure Auszug mit Äther   extrahiert, unter Eiskiihlung    mit konz. Natronlauge versetzt und das ausgeschiedene   61    in Äther aufgenommen. Nach dem Trocknen der   Ätherauszüge    über Pottasche wird der Äther verdampft und der Rüe-kstand im Hochvakuum getrocknet.



   Dabei gewinnt man das ¯-DiÏthylaminopropionsäure-N-   (3-o-acetamino-phenoxy-pro-    pyl-2)-methylamid in einer Ausbeute von   70"/o    der Theorie als farblose zähflüssige Masse, welche schwer   löslieh    in Wasser, gut in   organiselien    Lösungsmitteln und in verdünnten Mineralsäuren ist.



   Das Pikrat der Verbindung schmilzt bei   125-126".     



   PATENTANSPRUCH :
Verfahren zur Herstellung eines neuen basisch substituierten   Fettsäureamides,    dadurch gekennzeichnet, dass man eine Verbindung der Formel
EMI1.2     
 

**WARNUNG** Ende DESC Feld konnte Anfang CLMS uberlappen**.





  



  Process for the production of a new basic substituted fatty acid amide.



   The subject of the present patent forms a process for the preparation of a new basic substituted fatty acid amide, which is characterized in that a compound of the formula
EMI1.1
 in which X is a reactive radical which is split off during the reaction, is reacted with diethylamine.



   The radical X can be a halogen atom or some other reactive substituent suitable for replacement with the basic radical, such as an alkylsulfonyloxy or arylsulfonyloxy group. Group X is exchanged for the diethylamino radical, for example, by simply heating with diethylamine, optionally in the presence of a basic condensing agent or excess diethylamine. The p-diethylamino-propionic acid-N- (3-o-aeetamino-phenoxy-propyl-2) -meth, ylamide is a colorless, viscous mass. The picrate of the base melts at 125-126.



   The new amide will be used as a local anesthetic and as an intermediate for the production of other derivatives.



   Example:
5.5 g of S-bromo-propionic acid-N- (3-o-acet-amino-phenoxy-propyl-2) -methylamide and 7.3 g of diethylamine are dissolved together in 100 em3 abs. Benzene heated on a water bath for 3 hours. The reaction mixture is extracted with water and then extracted with 2N hydrochloric acid. The hydrochloric acid extract is then extracted with ether, with ice cooling with conc. Sodium hydroxide solution was added and the excreted 61 was taken up in ether. After the ether extracts have dried over potash, the ether is evaporated and the residue is dried in a high vacuum.



   The ¯-diethylaminopropionic acid-N- (3-o-acetaminophenoxy-propyl-2) -methylamide is obtained in a yield of 70 "/ o of theory as a colorless, viscous mass, which is sparingly soluble in water, well in organiselien solvents and in dilute mineral acids.



   The picrate of the compound melts at 125-126 ".



   PATENT CLAIM:
Process for the preparation of a new basic substituted fatty acid amide, characterized in that a compound of the formula
EMI1.2
 

** WARNING ** End of DESC field could overlap beginning of CLMS **.



 

Claims (1)

**WARNUNG** Anfang CLMS Feld konnte Ende DESC uberlappen **. ** WARNING ** Beginning of CLMS field could overlap end of DESC **. Verfahren zur Herstellung eines neuen basisch substituierten Fettsiureamides. Process for the production of a new basic substituted fatty acid amide. Gegenstand des vorliegenden Patentes bildet ein Verfahren zur Herstellung eines neuen basisch substituierten Fettsäureamides, welehes dadurch gekennzeichnet ist, dass man eine Verbindung der Formel EMI1.1 in welcher X einen reaktionsfähigen, während der Reaktion sich abspaltenden Rest bedeutet, mit Diäthylamin umsetzt. The subject of the present patent forms a process for the preparation of a new basic substituted fatty acid amide, which is characterized in that a compound of the formula EMI1.1 in which X is a reactive radical which is split off during the reaction, is reacted with diethylamine. Der Rest X kann in einem Halogenatom oder einem sonstigen für den Austausch gegen den basischen Rest geeigneten reaktionsfähi en Substituenten, wie zum Beispiel einer Alkylsulfonyloxy- oder Arylsulfonyloxygruppe, bestehen. Der Austausch der Gruppe X gegen den Diäthylaminorest erfolgt zum Beispiel durch einfaches Erwärmen mit Diäthylamin, gegebenenfalls in Gegenwart eines basisch reagierenden Kondensationsmittels oder von Diäthylamin im Überschuss. Das p-Diäthyl- amino-propionsäure-N-(3-o-aeetamino-phen- oxy-propyl-2)-meth, ylamid ist eine farblose zähflüssige Masse. Das Pikrat der Base sehmilzt bei 125-126 . The radical X can be a halogen atom or some other reactive substituent suitable for replacement with the basic radical, such as an alkylsulfonyloxy or arylsulfonyloxy group. Group X is exchanged for the diethylamino radical, for example, by simply heating with diethylamine, optionally in the presence of a basic condensing agent or excess diethylamine. The p-diethylamino-propionic acid-N- (3-o-aeetamino-phenoxy-propyl-2) -meth, ylamide is a colorless, viscous mass. The picrate of the base melts at 125-126. Das neue Amid soll als Lokalanästhetikum und als Zwischenprodukt zur Herstellung weiterer Derivate Verwendung finden. The new amide will be used as a local anesthetic and as an intermediate for the production of other derivatives. Beispiel : 5, 5 g S-Brom-propionsäure-N-(3-o-acet- amino-phenoxy-propyl-2)-methylamid und 7, 3 g Diäthylamin werden zusammen in 100 em3 abs. Benzol 3 Stunden auf dem Wasserbad erhitzt. Das Reaktionsgemisch wird mit Wasser ausgeschüttelt und dann mit 2n-Salzsäure ausgezogen. Darauf wird der salzsaure Auszug mit Äther extrahiert, unter Eiskiihlung mit konz. Natronlauge versetzt und das ausgeschiedene 61 in Äther aufgenommen. Nach dem Trocknen der Ätherauszüge über Pottasche wird der Äther verdampft und der Rüe-kstand im Hochvakuum getrocknet. Example: 5.5 g of S-bromo-propionic acid-N- (3-o-acet-amino-phenoxy-propyl-2) -methylamide and 7.3 g of diethylamine are dissolved together in 100 em3 abs. Benzene heated on a water bath for 3 hours. The reaction mixture is extracted with water and then extracted with 2N hydrochloric acid. The hydrochloric acid extract is then extracted with ether, cooled with ice with conc. Sodium hydroxide solution was added and the excreted 61 was taken up in ether. After the ether extracts have been dried over potash, the ether is evaporated and the residue is dried in a high vacuum. Dabei gewinnt man das ¯-DiÏthylaminopropionsäure-N- (3-o-acetamino-phenoxy-pro- pyl-2)-methylamid in einer Ausbeute von 70"/o der Theorie als farblose zähflüssige Masse, welche schwer löslieh in Wasser, gut in organiselien Lösungsmitteln und in verdünnten Mineralsäuren ist. The ¯-diethylaminopropionic acid-N- (3-o-acetaminophenoxy-propyl-2) -methylamide is obtained in a yield of 70 "/ o of theory as a colorless, viscous mass, which is sparingly soluble in water, well in organiselien solvents and in dilute mineral acids. Das Pikrat der Verbindung schmilzt bei 125-126". The picrate of the compound melts at 125-126 ". PATENTANSPRUCH : Verfahren zur Herstellung eines neuen basisch substituierten Fettsäureamides, dadurch gekennzeichnet, dass man eine Verbindung der Formel EMI1.2 in welcher X einen reaktionsfahigen, während der Reaktion sich abspaltenden Rest bedeutet, mit Diäthylamin umsetzt. Das auf diese Weise erhaltene, ¯- DiÏthylamino-propionsÏure-N - (3 o - a@@tamino - phenoxy - propyl - 2) -methylamid bildet eine farblose, zÏhfl ssige Masse. Das Pikrat der Base schmilzt bei 125-126 . PATENT CLAIM: Process for the preparation of a new basic substituted fatty acid amide, characterized in that a compound of the formula EMI1.2 in which X is a reactive radical which is split off during the reaction, is reacted with diethylamine. The ¯-diethylamino-propionic acid-N - (3 o - a @@ tamino-phenoxy-propyl-2) -methylamide obtained in this way forms a colorless, viscous mass. The picrate of the base melts at 125-126. Das neue Amid soll als Lokalanästhetikum und als Zwischenprodukt Verwendung finden. The new amide will be used as a local anesthetic and as an intermediate product. UNTERANSPBUCH: Verfahren nach Patentanspruch, dadureh gekennzeichnet, dass man ein ss-Halogen-pro- pionsäure-N- (3-o-acetamino-phenoxy-propyl -2)-methy] amid mit DiÏthylamin reagieren lϯt. SUB-CLAIM: Process according to patent claim, characterized in that an β-halo-propionic acid-N- (3-o-acetaminophenoxypropyl -2) -methy] amide is allowed to react with diethylamine.
CH311673D 1952-06-08 1952-06-08 Process for the production of a new basic substituted fatty acid amide. CH311673A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH311673T 1952-06-08
CH307799T 1952-11-25

Publications (1)

Publication Number Publication Date
CH311673A true CH311673A (en) 1955-11-30

Family

ID=25735406

Family Applications (1)

Application Number Title Priority Date Filing Date
CH311673D CH311673A (en) 1952-06-08 1952-06-08 Process for the production of a new basic substituted fatty acid amide.

Country Status (1)

Country Link
CH (1) CH311673A (en)

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