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CH311587A - Process for making a new salt. - Google Patents

Process for making a new salt.

Info

Publication number
CH311587A
CH311587A CH311587DA CH311587A CH 311587 A CH311587 A CH 311587A CH 311587D A CH311587D A CH 311587DA CH 311587 A CH311587 A CH 311587A
Authority
CH
Switzerland
Prior art keywords
anilide
acid
chloro
methyl
making
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 CH311587A publication Critical patent/CH311587A/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

  

  Verfahren zur     Herstellung    eines neuen Salzes.    Gegenstand des vorliegenden Patentes ist  ein Verfahren zur Herstellung eines neuen  Salzes, welches dadurch gekennzeichnet ist,  dass man     N-Pyrrolidinoessigsäure-(2-chlor-6-          methyl-anilid)    mit     Citronensäure    zur Reak  tion bringt. Man kann die     Umsetzung    in  einem Lösungsmittel, wie z. B. Alkohol, Äther,  Benzol,     Dioxan,    Wasser,     Wasser-Alkoholgemi-          sehen,    vornehmen.  



  Man kann     zur        Ausfiihrung    des     erfindungs-          ;remässen    Verfahrens auch so vorgehen, dass  man ein solches Salz des     N-Pyrrolidinoessig-          -,äure-(2-elilor-6-methyl-anilides)    mit einem  solchen Salz der     Citronensäure    zusammen  bringt, aus welchen sich durch Umsetzung       intermediär    das freie     N-Pyrrolidinoessigsätire-          2-ch@oi-b-incahyl-ani@id    ) und die freie     Citro-          nensäure    bilden.

   Das Reaktionsprodukt be  steht in diesem Falle aus zwei Salzen; je nach       fier        Löslichkeit    und     Kristallisationstendenz          derselben    tritt das     N-PSu#rolidinoessigsäure-(2-          ehlor-6-inethyl-anilid)-dihydrogencitrat    als er  stes oder als zweites     Kristallisat    auf.  



  Das so erhaltene     N-Pyrrolidinoessigsäure-          (2-ehlor-6-methyl-anilid)-dihydrogencitrat    bil  det farblose Kristalle, die bei     1,58-160(1    unter    Zersetzung schmelzen. Das neue Salz soll als  Lokalanästhetikum verwendet werden.    <I>Beispiel:</I>    5     g        N-Pyrrolidinoessigsäure-(2-chlor-6-me-          thyl-anilid)    in 7     cm3    Aceton werden mit einer  Lösung von 3,8 g     Citronensäure    in 13     cm3     Aceton versetzt.

   Nach kurzer Zeit tritt Kri  stallisation     ein.    Nach einiger Zeit.     werden    die  gebildeten Kristalle abgesaugt, mit Äther ge  waschen und dann getrocknet. Man erhält 7 g  des bei 1.58-160  unter Zersetzung schmel  zenden     N-Pyrrolidinoessigsäure-(2-chlor-6-me-          thyl-anilid)        -dihydrogencitrates.  



  Process for making a new salt. The subject of the present patent is a process for the production of a new salt which is characterized in that N-pyrrolidinoacetic acid (2-chloro-6-methyl-anilide) is reacted with citric acid. You can do the reaction in a solvent, such as. B. alcohol, ether, benzene, dioxane, water, water-alcohol mixtures see, make.



  To carry out the method according to the invention, one can also proceed in such a way that such a salt of N-pyrrolidinoacetic acid (2-elilor-6-methyl-anilide) is brought together with such a salt of citric acid the free N-pyrrolidinoacetic acid-2-ch @ oi-b-incahyl-ani @ id) and the free citric acid are formed as intermediates by reaction.

   The reaction product consists of two salts in this case; Depending on the solubility and crystallization tendency of the same, the N-PSu # rolidinoacetic acid (2-chloro-6-ynethyl anilide) dihydrogen citrate occurs as the first or second crystallizate.



  The N-pyrrolidinoacetic acid (2-chloro-6-methyl-anilide) dihydrogen citrate obtained in this way forms colorless crystals which melt at 1.58-160 (1 with decomposition. The new salt is to be used as a local anesthetic. <I> Example: 5 g of N-pyrrolidinoacetic acid (2-chloro-6-methyl anilide) in 7 cm3 of acetone are mixed with a solution of 3.8 g of citric acid in 13 cm3 of acetone.

   Crystallization occurs after a short time. After some time. the crystals formed are suctioned off, washed with ether and then dried. 7 g of N-pyrrolidinoacetic acid (2-chloro-6-methyl anilide) dihydrogen citrate, which melts at 1.58-160 with decomposition, are obtained.

 

Claims (1)

PATBNTANSPRUCII Verfahren zur Herste11iuig eines neuer. Salzes, dadurch gekennzeichnet, dass man N- Pyrrolidinoessigsäure - (? - chlor - 6 -methyl-ani- lid) mit Citronensäure zur Reaktion bringt.. Das resultierende N-Pyrrolidinoessigsäur e- (2-chlor-6-methyl-anilid)-dihydrogencitrat bil det farblose, bei 158-160 unter Zersetzung schmelzende Kristalle; es soll als Lokalanästhe tikum verwendet werden. PATBNTANSPRUCII Process for the production of a new one. Salt, characterized in that N-pyrrolidinoacetic acid - (? - chloro - 6-methyl-anilide) is reacted with citric acid. The resulting N-pyrrolidino-acetic acid e- (2-chloro-6-methyl-anilide) - dihydrogen citrate forms colorless crystals that melt at 158-160 with decomposition; it is intended to be used as a local anesthetic.
CH311587D 1952-02-25 1952-02-25 Process for making a new salt. CH311587A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH311587T 1952-02-25
CH306793T 1955-04-30

Publications (1)

Publication Number Publication Date
CH311587A true CH311587A (en) 1955-11-30

Family

ID=25735205

Family Applications (1)

Application Number Title Priority Date Filing Date
CH311587D CH311587A (en) 1952-02-25 1952-02-25 Process for making a new salt.

Country Status (1)

Country Link
CH (1) CH311587A (en)

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