CH94949A - Process for the preparation of the calcium salt of benzylphthalamic acid. - Google Patents

Process for the preparation of the calcium salt of benzylphthalamic acid.

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Publication number
CH94949A
CH94949A CH94949DA CH94949A CH 94949 A CH94949 A CH 94949A CH 94949D A CH94949D A CH 94949DA CH 94949 A CH94949 A CH 94949A
Authority
CH
Switzerland
Prior art keywords
acid
benzylphthalamic
calcium salt
salt
preparation
Prior art date
Application number
Other languages
German (de)
Inventor
F Hoffmann- Aktiengesellschaft
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of CH94949A publication Critical patent/CH94949A/en

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Classifications

    • 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
    • C07C233/12Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups

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

Description

  

  Verfahren zur Darstellung des     Italeiumsalzes    der     Benzylphtalamidsäure.       Das     Calciumsalz    der     Benzylphtalamidsäure     ist bis jetzt noch nicht bekannt geworden.  Seine wässerigen Lösungen neigen, wie die  jenigen des     Natriumsalzes,    namentlich in der  Wärme zur Zersetzung unter Bildung von       Benzylphtaiimid.     



  Es wurde nun gefunden, dass man das       Calciumsalz    der     Benzylphtalamidsäure    da  durch erhält, wenn man dasselbe aus den  zweckmässig heissen, wässerigen Lösungen,  die gleichzeitig freies .     Calciumhydroxyd    ent  halten, auskristallisieren lässt.  



  Das     Calciumsalz    'der     Benzyl.phtalamid-          säure    kristallisiert aus seiner in der Wärme  gesättigten Lösung in Nadeln aus. In kaltem  Wasser ist es schwer, in heissem leicht löslich.  Säuren fällen aus der wässerigen Lösung die  freie     Benzylphtalamidsäure.    Es hat die Eigen  schaft, trotz seiner Wasserlöslichkeit     spasmo-          lytisch    zu wirken, und ist durch eine äusserst  geringe Toxizität ausgezeichnet; daher soll       t,s    in der Therapie Verwendung finden.  



  <I>Beispiel</I>     r:     7 0 Teile reines     Benzylphtalimid    werden  mit 2000 Teilen einer dünnen, feinen Kalk  milch, die 15 Teile     Calciumhydroxyd    enthält,    so lauge bei 80 bis 90   verrührt, bis das       Benzylphtalimid    völlig in Lösung gegangen  ist, wozu etwa drei Stunden erforderlich sind.  Darauf filtriert man von Spuren ungelöstem       Falk    ab und lässt unter     Luftabschluss    erkalten.  Aus der Lösung kristallisiert das     Calciumsalz     der     Benzylphtalamidsäure.     



  <I>Beispiel 2:</I>       474    Teile rohes     Benzylphtalimid    (Berichte  der deutschen chemischen Gesellschaft, 20,  <B>1887,</B> Seite 2227) werden mit 1000 Teilen  10      'oiger,    siedend heisser Natronlauge über  gossen und so lange verrührt, bis alles     Benzyl-          phtalimid    in Lösung gegangen ist.

   Darauf  verdünnt man in kaltem -Wasser auf 7000  Teile, neutralisiert mit Essigsäure und ver  rührt die Lösung in der gälte während 12  bis 24 Stunden mit<B>LA</B>     ntfärbungskohle.    Fil  triert man nun von dem unlöslichen Anteil ab,  so erhält man ein fast farbloses Filtrat, zu dem  man eine Lösung von 800     gr    kristallisiertem       Chlorcalcium    in 250 Teilen Wasser setzt.  Die Hauptmenge der     Benzylphtalamidsäure     kristallisiert darauf als     Kalksalz    aus.

   Das  Kalksalz wird zwecks völliger Reinigung  aus mit Ätzkalk alkalisch gestelltem Wasser           umkristallisiert.        rin    auf diese Weise er  haltenes, bei 1002     getrocknetes    Salz zeigt  folgenden     Caleiumgehalt:     Ca: gefunden 7,38 %,  berechnet für     (C15H"03)2    Ca.  Ca: - 7,31



  Process for the preparation of the Italian salt of benzylphthalamic acid. The calcium salt of benzylphthalamic acid has not yet become known. Its aqueous solutions, like those of the sodium salt, tend to decompose when exposed to heat, with the formation of benzylphthalimide.



  It has now been found that the calcium salt of benzylphtalamic acid is obtained if the same is obtained from the appropriately hot, aqueous solutions which are simultaneously free. Calcium hydroxide contains, lets crystallize.



  The calcium salt of benzyl phthalamic acid crystallizes out in needles from its solution which is saturated with heat. It is difficult to dissolve in cold water and easily soluble in hot water. Acids precipitate the free benzylphthalamic acid from the aqueous solution. It has the property of having a spasmolytic effect in spite of its solubility in water, and is distinguished by its extremely low toxicity; therefore t, s should be used in therapy.



  <I> Example </I> r: 7 0 parts of pure benzyl phthalimide are mixed with 2000 parts of a thin, fine milk of lime containing 15 parts of calcium hydroxide in a solution at 80 to 90, until the benzyl phthalimide has completely dissolved, including about three hours are required. Then filter off traces of undissolved Falk and leave to cool in the absence of air. The calcium salt of benzylphthalamic acid crystallizes out of the solution.



  <I> Example 2: </I> 474 parts of crude benzylphthalimide (reports of the German chemical society, 20, <B> 1887, </B> page 2227) are poured over with 1000 parts of 10%, boiling hot sodium hydroxide solution and so on Stirred for a long time until all the benzyl phthalimide has gone into solution.

   The mixture is then diluted to 7000 parts in cold water, neutralized with acetic acid and the solution is stirred in the cold for 12 to 24 hours with <B> LA </B> non-coloring charcoal. If the insoluble fraction is filtered off, an almost colorless filtrate is obtained, to which a solution of 800 g of crystallized calcium chloride in 250 parts of water is added. Most of the benzylphthalamic acid then crystallizes out as a lime salt.

   The lime salt is recrystallized from water made alkaline with quick lime for the purpose of complete purification. The salt obtained in this way and dried at 1002 shows the following calcium content: Ca: found 7.38%, calculated for (C15H "03) 2 Ca. Ca: - 7.31

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung des Calcium- salzes der Benzylphtalamidsäure, dadurch ge kennzeichnet, dass man das Salz aus seinen j < ässerigen Lösungen, die gleichzeitig freies Calciumhy droxyd enthalten, auskristallisieren lässt. Das Caleiumsalz der 13enzylphtalamid- säure kristallisiert aus seiner in der Wärme gesättigten Lösung in Nadeln aus. PATENT CLAIM: Process for the preparation of the calcium salt of benzylphthalamic acid, characterized in that the salt is allowed to crystallize out of its aqueous solutions, which also contain free calcium hydroxide. The calcium salt of 13enzylphtalamidic acid crystallizes out in needles from its solution saturated with heat. In kaltem Wasser ist es schwer, in heissem leicht löslich. Säuren fällen aus der wässerigen Lösung die freie Benzylphtalamidsäure. Es hat die Eigen schaft, trotz seiner Wasserlöslichkeit spasmo- lytisch zu wirken, und ist durch eine äusserst geringe Toxizität ausgezeichnet: daher soll es in der Therapie Verwendung finden. It is difficult to dissolve in cold water and easily soluble in hot water. Acids precipitate the free benzylphthalamic acid from the aqueous solution. It has the property of having a spasmolytic effect despite its solubility in water, and is characterized by its extremely low toxicity: therefore it should be used in therapy.
CH94949D 1921-03-05 1921-03-05 Process for the preparation of the calcium salt of benzylphthalamic acid. CH94949A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH94949T 1921-03-05

Publications (1)

Publication Number Publication Date
CH94949A true CH94949A (en) 1922-06-01

Family

ID=4352592

Family Applications (1)

Application Number Title Priority Date Filing Date
CH94949D CH94949A (en) 1921-03-05 1921-03-05 Process for the preparation of the calcium salt of benzylphthalamic acid.

Country Status (1)

Country Link
CH (1) CH94949A (en)

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