CH246387A - Process for the preparation of an ephedrine derivative. - Google Patents

Process for the preparation of an ephedrine derivative.

Info

Publication number
CH246387A
CH246387A CH246387DA CH246387A CH 246387 A CH246387 A CH 246387A CH 246387D A CH246387D A CH 246387DA CH 246387 A CH246387 A CH 246387A
Authority
CH
Switzerland
Prior art keywords
ephedrine
preparation
derivative
bromo
ephedrine derivative
Prior art date
Application number
Other languages
German (de)
Inventor
H Dr Herzog
Original Assignee
H Dr Herzog
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 H Dr Herzog filed Critical H Dr Herzog
Publication of CH246387A publication Critical patent/CH246387A/en

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  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

      Verfahren        zur        Herstellung        eines        Ephedrinderivates.            Ephedrin    und dessen Salze werden in der  Therapie zur Reizung de     Sympathicus    an  gewandt. Diese Stoffe haben aber eine starke       blutdrucksteigernde    Wirkung, so dass sie  z. B. hauptsächlich bei der Behandlung älte  rer Patienten nicht zur Anwendung kommen  können.  



  Die vorliegende Erfindung betrifft nun  ein Verfahren zur     Herstellung    eines     Ephe-          drinderivates,    das dadurch gekennzeichnet  ist, dass man     Ephedrin    mit     a-Brom-isoval@e-          riansäure    umsetzt. Das so erhaltene     Ephedrin-          a-bromisovalerianat    ist eine weisse, kristalli  sierte, wasserlösliche Substanz, die bei       12-9-1.311     C schmilzt und zu pharmazeu  tischen Zwecken Verwendung finden soll.  



  Das     Ephedrin-a-brom-isovalerianat    hat  z. B: neben der bekannten     Ephedrin-Wir-          kung    den Vorteil, in geringerem Masse als die  bisher bekannten     Ephedrinpräparate    den  Blutdruck zu     steigern.    Ausserdem zeigt das  neue Produkt durch die     Sedativ-Komponente     der     Brom-isovaleriansäureeine    stark desensi  bilisierende Wirkung gegen Allergene im    allgemeinen und wirkt insbesondere bei mit  Juckreiz verbundenen allergischen Zuständen  beruhigend.  



  <I>Beispiel:</I>  165 g     Ephedrin    werden mit<B>181</B> g     a-Brom-          isovaleriansäure        unter    starkem Schütteln ver  mischt, einige Stundenstehen gelassen. wobei  sich das kristallisierte     Ephedrin-a-brom-iso-          valerianat        ausscheidet.    Die     Kristalle    werden  durch     Umkristallisieren    aus Methanol     gerei-          nizt.  



      Process for the preparation of an ephedrine derivative. Ephedrine and its salts are used in therapy to stimulate the sympathetic nervous system. However, these substances have a strong blood pressure-increasing effect, so that they B. mainly in the treatment of elderly patients can not be used.



  The present invention relates to a process for the production of an epherrin derivative, which is characterized in that ephedrine is reacted with a-bromo-isoval @ eric acid. The ephedrine a-bromoisovalerianate obtained in this way is a white, crystallized, water-soluble substance which melts at 12-9-1,311 C and is intended to be used for pharmaceutical purposes.



  The ephedrine-a-bromine isovalerate z. B: In addition to the well-known ephedrine effect, the advantage of increasing blood pressure to a lesser extent than the previously known ephedrine preparations. In addition, thanks to the sedative component of bromoisovaleric acid, the new product has a strong desensitizing effect against allergens in general and has a calming effect in particular in allergic conditions associated with itching.



  <I> Example: </I> 165 g ephedrine are mixed with <B> 181 </B> g a-bromo-isovaleric acid with vigorous shaking, left to stand for a few hours. the crystallized ephedrine-a-bromo-isovalerianate separates out. The crystals are purified by recrystallization from methanol.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Ephe- drinderivates, dadurch gekennzeichnet, dass man Ephedrin mit a-Brom-is@ovaleriansäure umsetzt. Das so erhaltene Ephedrin-a-broM-iso- valerianat ist eine weisse, kristalline, wasser lösliche Substanz, die bei 129-131 C schmilzt und zu pharmazeutischen Zwecken Verwendung finden soll. PATENT CLAIM: Process for the production of an ephe- drine derivative, characterized in that ephedrine is reacted with a-bromo-is @ ovaleric acid. The ephedrine-a-broM-isovalerate obtained in this way is a white, crystalline, water-soluble substance which melts at 129-131 C and is intended to be used for pharmaceutical purposes.
CH246387D 1945-06-12 1945-06-12 Process for the preparation of an ephedrine derivative. CH246387A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH246387T 1945-06-12

Publications (1)

Publication Number Publication Date
CH246387A true CH246387A (en) 1946-12-31

Family

ID=4465506

Family Applications (1)

Application Number Title Priority Date Filing Date
CH246387D CH246387A (en) 1945-06-12 1945-06-12 Process for the preparation of an ephedrine derivative.

Country Status (1)

Country Link
CH (1) CH246387A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008071948A2 (en) * 2006-12-12 2008-06-19 Sosei R & D Ltd. Aminoalcohol derivatives and their therapeutic use

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008071948A2 (en) * 2006-12-12 2008-06-19 Sosei R & D Ltd. Aminoalcohol derivatives and their therapeutic use
WO2008071948A3 (en) * 2006-12-12 2008-07-31 Sosei R & D Ltd Aminoalcohol derivatives and their therapeutic use

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