CH259681A - Process for the preparation of a biguanide derivative. - Google Patents

Process for the preparation of a biguanide derivative.

Info

Publication number
CH259681A
CH259681A CH259681DA CH259681A CH 259681 A CH259681 A CH 259681A CH 259681D A CH259681D A CH 259681DA CH 259681 A CH259681 A CH 259681A
Authority
CH
Switzerland
Prior art keywords
preparation
methyl
iodophenyl
biguanide derivative
acid
Prior art date
Application number
Other languages
German (de)
Inventor
Limited Imperial Ch Industries
Original Assignee
Ici Ltd
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 Ici Ltd filed Critical Ici Ltd
Publication of CH259681A publication Critical patent/CH259681A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C279/00Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C279/20Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups containing any of the groups, X being a hetero atom, Y being any atom, e.g. acylguanidines
    • C07C279/24Y being a hetero atom
    • C07C279/26X and Y being nitrogen atoms, i.e. biguanides

Landscapes

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

Description

  

  Verfahren zur Herstellung eines     Biguanidderivates.       Die vorliegende Erfindung betrifft ein  Verfahren zur Herstellung von     Nl-p-Jod-          phenyl-N'-methyl-N'-n-propylbiguanid,        wel-          ehes    ein wertvolles chemotherapeutisches Mit  tel ist oder als Zwischenprodukt für die Her  stellung von chemotherapeutischen Mitteln  verwendet werden kann. Es ist insbesondere  ein wertvolles     Antimalariamittel.     



  Erfindungsgemäss wird die besagte neue  Verbindung, nämlich     N1    - p -     Jodphenyl-N'-          niethyl-N'-ii-propylbiguanid,    dadurch erhal  ten, dass man     N3-i@lethyl-N'-n-propyldieyan-          diamid    mit     p-Jodanilin    umsetzt.  



  Die Unisetzung erfolgt zweckmässig durch  Erhitzen eines Salzes des Amins mit dem sub  stituierten     Dicyandiamid    in Gegenwart eines  Lösungsmittels, wie z. B. Wasser oder     ss-          Äthoxyäthanol.     



  Das     Nl-p-Jodphenyl-N'-methyl-N'-n-pro-          pylbiguanid    stellt eine starke Base dar, welche  mit organischen und anorganischen Säuren  beständige Salze ergibt, die in manchen Fäl  len in Wasser leicht löslich sind. Die Salze  lassen sich dadurch herstellen, dass die Base  in     ,wässrigen    Lösungen der Säure gelöst und  hierauf das Wasser verdampft wird, doch  können sie in trockener Form bequemer durch  Vermischen der Komponenten in einem orga  nischen Lösungsmittel, wie z. B. Aceton, oder  in einem Alkohol, in welchem die Salze spär  lich löslich sind, hergestellt werden.

   Auf diese  Weise kann man beispielsweise die Salze mit    Essigsäure, Milchsäure,     Methanstilfonsäure,          Methylendisalicylsäure,        Methylen-bis-ss-oxy-          i!.aphthoesättre    und Salzsäure bequem her  stellen.  



  Das folgende Beispiel diene zur Erläute  rung der Erfindung.    <I>Beispiel:</I>  Ein Gemisch von 18 Teilen     N3-Methyl-N3-          n-propyldicyandiamid    und 30 Teilen     p-Jod-          a.nilin-chlorhydrat    in 50 Teilen Wasser wird  während 3 Stunden unter     Rückfluss    zum Sie  den erhitzt. Hierauf lässt man das Gemisch  abkühlen, worauf     abfiltriert    wird. Der feste  Rückstand wird mit kaltem Wasser gewaschen  und aus Wasser umkristallisiert.

   Auf diese  Weise erhält man     Nl-p-Jodphenyl-N'-methyl-          N'-n-propylbiguanid    in Form seines     Mono-          hydrochlorids,    welches bei 238  C schmilzt.



  Process for the preparation of a biguanide derivative. The present invention relates to a process for the preparation of Nl-p-iodophenyl-N'-methyl-N'-n-propylbiguanide, which is a valuable chemotherapeutic agent before or is used as an intermediate for the manufacture of chemotherapeutic agents can. It is a particularly valuable antimalarial drug.



  According to the invention, said new compound, namely N1 - p - iodophenyl-N'-niethyl-N'-ii-propylbiguanide, is obtained by adding N3-i @ lethyl-N'-n-propyldiyaniamide with p-iodoaniline implements.



  It is conveniently carried out by heating a salt of the amine with the sub-substituted dicyandiamide in the presence of a solvent, such as. B. water or ss- ethoxyethanol.



  The Nl-p-iodophenyl-N'-methyl-N'-n-propylbiguanide is a strong base which, with organic and inorganic acids, gives stable salts, which in some cases are easily soluble in water. The salts can be prepared in that the base is dissolved in aqueous solutions of the acid and then the water is evaporated, but they can be more convenient in dry form by mixing the components in an orga African solvent, such as. B. acetone, or in an alcohol in which the salts are sparse Lich soluble, are produced.

   In this way, for example, the salts with acetic acid, lactic acid, methanesilfonic acid, methylenedisalicylic acid, methylene-bis-ss-oxy- i .aphthoic acid and hydrochloric acid can be conveniently prepared.



  The following example serves to explain the invention. <I> Example: </I> A mixture of 18 parts of N3-methyl-N3-n-propyldicyandiamide and 30 parts of p-iodine-a.niline chlorohydrate in 50 parts of water is refluxed for 3 hours. The mixture is then allowed to cool and it is filtered off. The solid residue is washed with cold water and recrystallized from water.

   In this way, Nl-p-iodophenyl-N'-methyl-N'-n-propylbiguanide is obtained in the form of its monohydrochloride, which melts at 238.degree.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung von Nl-p-Jod- phenyl -N' - methyl -N 1- n - propylbiguanid, da durch gekennzeichnet, dass man N3-Methyl-N3- n-propyldicyandiamid mit p-Jodanilin um setzt. Das Nl-p-Jodphenyl-N'-methyl-N'-n-pro- py3biguanid ist eine starke Base, deren Mono- hydrochlorid bei 238 C schmilzt. Die neue Base besitzt kräftige Antimalariaeigenschaften. PATENT CLAIM: Process for the production of Nl-p-iodophenyl -N'-methyl -N 1- n -propylbiguanide, characterized in that N3-methyl-N3-n-propyldicyandiamide is implemented with p-iodoaniline. The Nl-p-iodophenyl-N'-methyl-N'-n-propy3biguanid is a strong base whose monohydrochloride melts at 238 ° C. The new base has powerful anti-malarial properties.
CH259681D 1945-10-08 1946-10-08 Process for the preparation of a biguanide derivative. CH259681A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB259681X 1945-10-08
GB170946X 1946-09-17
CH254800T 1946-10-08

Publications (1)

Publication Number Publication Date
CH259681A true CH259681A (en) 1949-01-31

Family

ID=27178037

Family Applications (1)

Application Number Title Priority Date Filing Date
CH259681D CH259681A (en) 1945-10-08 1946-10-08 Process for the preparation of a biguanide derivative.

Country Status (1)

Country Link
CH (1) CH259681A (en)

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