CH188550A - Process for the preparation of a quinine compound with poor taste. - Google Patents

Process for the preparation of a quinine compound with poor taste.

Info

Publication number
CH188550A
CH188550A CH188550DA CH188550A CH 188550 A CH188550 A CH 188550A CH 188550D A CH188550D A CH 188550DA CH 188550 A CH188550 A CH 188550A
Authority
CH
Switzerland
Prior art keywords
quinine
water
preparation
poor taste
acid
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 CH188550A publication Critical patent/CH188550A/en

Links

Landscapes

  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Description

  

  Verfahren zur Darstellung einer geschmacksschwachen     Chininverbindung.       Es wurde gefunden, dass das Chinin mit  der 2,3 -     Dioxynaphthalin-0-monoessigsäure     ein in Wasser     schwerlösliches    Salz bildet, in  welchem der bittere Geschmack des Alka  loids fast völlig verschwunden     ist.     



  Zur Herstellung der     neuen    Verbindung       wird    ein wasserlösliches     Chininsalz    mit  einem wasserlöslichen Salz der     2,3-Dioxy-          naphthalin-0-monoessigsäure    in wässeriger  Lösung zur Umsetzung gebracht.  



  Das 2,3 -     dioxynaphthalin    - 0 - monoessig  saure Chinin     kristallisiert    in Nadeln vom  Schmelzpunkt<B>195</B>  . Es ist praktisch ge  schmacksfrei. In Wasser ist es schwer, in  Alkohol ziemlich schwer löslich. Es soll als  Arzneimittel Verwendung finden.  



  <I>Beispiel:</I>  160 Teile     2,3-Dioxynaphthalin    werden  zusammen mit 95 Teilen Chloressigsäure in  700     Teilen    Wasser am     uTasserbad    gelöst;  dann     wird    unter     Schwenken    eine     Lösung    von    112 Teilen     Kaliumhydroxyd,    gelöst     in    300  Teilen Wasser, innerhalb einer Stunde zuge  geben. Nach weiteren zwei     Stunden    wird er  kalten gelassen, der ausgeschiedene Kristall  brei abgesaugt, und mit etwas Alkohol oder  Äther gewaschen.

   Aus dem Extrakt erhält  man unverändert     gebliebenes        2,3-Diogynaph-          thalin    zurück. Das     galiumsalz    der     2,3-          Dioxynaphthälin-0-monoessigsäure        wird    mit       verdünnter    Salzsäure erwärmt.     Beim    Erkal  ten scheidet sich die freie Säure in langen       nadeligen    Prismen ab, die bei<B>157'</B> unter Auf  schäumen schmelzen. Die Säure     ist    sehr  leicht in Alkohol,     ,schwer    in kaltem, ziemlich  in     warmem    Wasser löslich.  



  240     Gewichtsteile    2,3 -     diogynaphthaJin-          0-essigsaures        Natrium    werden     in    5000 Ge  wichtsteilen     heissem    Wasser gelöst und die  Mischung noch     warm.    unter     Rühren    in eine  Lösung von     3,80    Gewichtsteilen     kristallisier-          tes        Chininhydrochlorid        einfliessen    gelassen.  Das gebildete 2,3-Hoxynaphthab.u-0-essig-      saure     Chinin    scheidet sich sofort kristallisiert  aus.

   Nach dem Erkalten     ist        die    Fällung voll  ständig. Man saugt ab und trocknet bei 80  bis 100  .



  Process for the preparation of a quinine compound with poor taste. It was found that quinine and 2,3-dioxynaphthalene-0-monoacetic acid form a salt which is sparingly soluble in water and in which the bitter taste of the alkali has almost completely disappeared.



  To produce the new compound, a water-soluble quinine salt is reacted with a water-soluble salt of 2,3-dioxynaphthalene-0-monoacetic acid in aqueous solution.



  The 2,3 - dioxynaphthalene - 0 - monoacetic acid quinine crystallizes in needles with a melting point of <B> 195 </B>. It is practically tasteless. It is difficult to dissolve in water and rather difficult to dissolve in alcohol. It is said to be used as a medicine.



  <I> Example: </I> 160 parts of 2,3-dioxynaphthalene are dissolved together with 95 parts of chloroacetic acid in 700 parts of water in a water bath; then a solution of 112 parts of potassium hydroxide, dissolved in 300 parts of water, is added over the course of an hour while swirling. After a further two hours it is left cold, the precipitated crystal pulp is sucked off and washed with a little alcohol or ether.

   2,3-Diogynaphthalene which has remained unchanged is obtained from the extract. The galium salt of 2,3-dioxynaphthalene-0-monoacetic acid is heated with dilute hydrochloric acid. When it cools down, the free acid is deposited in long needle-like prisms, which melt at <B> 157 '</B> while foaming. The acid is very easily soluble in alcohol, difficult in cold, fairly warm water.



  240 parts by weight of 2,3-diogynaphthaJin- 0-acetic acid sodium are dissolved in 5000 parts by weight of hot water and the mixture is still warm. allowed to flow into a solution of 3.80 parts by weight of crystallized quinine hydrochloride with stirring. The 2,3-hoxynaphthab.u-0-acetic acid quinine formed precipitates immediately in crystallized form.

   After cooling, the precipitation is complete. It is suctioned off and dried at 80 to 100.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung einer ge schmacksschwachen Chininverbindung, da durch gekennzeichnet, dass man ein wasser lösliches Chinin salz mit einem wasserlös- liehen Salz der $: PATENT CLAIM: Process for the preparation of a tasteless quinine compound, characterized in that a water-soluble quinine salt is mixed with a water-soluble salt of $: ,8-1)logynaplithalin-0-mono- essigsäure in wässeriger Lösung umsetzt. Das<B>2,3</B> - .diogynaphthalin - 0 - monoessig saure Chinin kristallisiert in Nadeln vom Schmelzpunkt 195 . Es ist praktisch ge schmacksfrei. In Wasser ist es schwer, in Alkohol ziemlich schwer löslich. Es soll als Arzneimittel Verwendung finden. , 8-1) logynaplithalin-0-mono-acetic acid in aqueous solution. The <B> 2,3 </B> - .diogynaphthalene - 0 - monoacetic acid quinine crystallizes in needles with a melting point of 195. It is practically tasteless. It is difficult to dissolve in water and rather difficult to dissolve in alcohol. It is said to be used as a medicine.
CH188550D 1934-08-18 1935-07-18 Process for the preparation of a quinine compound with poor taste. CH188550A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE188550X 1934-08-18
CH183802T 1935-07-18

Publications (1)

Publication Number Publication Date
CH188550A true CH188550A (en) 1936-12-31

Family

ID=25720920

Family Applications (1)

Application Number Title Priority Date Filing Date
CH188550D CH188550A (en) 1934-08-18 1935-07-18 Process for the preparation of a quinine compound with poor taste.

Country Status (1)

Country Link
CH (1) CH188550A (en)

Similar Documents

Publication Publication Date Title
CH188550A (en) Process for the preparation of a quinine compound with poor taste.
AT145615B (en) Process for the preparation of a quinine compound with poor taste.
AT126160B (en) Process for the preparation of aminoketo alcohols.
AT117475B (en) Process for the preparation of substitution products of ß-iodopyridine.
DE504681C (en) Process for the production of pharmaceutical preparations
CH312530A (en) Process for making a pyridazone.
AT143480B (en) Process for the preparation of a quinine compound.
AT203000B (en) Process for the preparation of new salts of 4,6-dioxyisophthalic acid and 5-halogen (especially 5-iodine) - 4,6-dioxyisophthalic acid
DE859154C (en) Process for the preparation of Schiff bases of p-aminosalicylic acid
CH168947A (en) Process for the preparation of a derivative of 5,5-phenylaethylhydantoin.
CH183802A (en) Process for the preparation of a quinine compound with poor taste.
AT147483B (en) Process for the preparation of compounds of methyl N-methyltetrahydronicotinate.
AT56874B (en) Process for the preparation of esters of the hydroquina alkaloids
DE547984C (en) Process for the preparation of compounds of the alkali salts C, C-disubstituted barbituric acids with pyrazolones
DE498748C (en) Process for the preparation of derivatives on the 5-carbon atom of disubstituted barbituric acids
DE234631C (en)
AT152300B (en) Process for the preparation of guaiacol compounds.
DE357752C (en) Process for the preparation of N-aminoacetyl compounds of 4-amino-1-phenyl-2íñ3-dialkyl-5-pyrazolones
CH185358A (en) Process for producing an azo compound.
CH276621A (en) Process for the preparation of p-amino-salicylic acid-n-butylmide.
CH230435A (en) Process for the production of a therapeutically valuable salt.
CH183066A (en) Method for preparing a salicylic acid compound.
CH169259A (en) Process for the preparation of a compound of Sparteine with phenylethylbarbituric acid.
CH237503A (en) Process for the preparation of 4-amino-benzene-sulfonylaminomethanesulfonic acid.
CH155047A (en) Process for the preparation of 3-dimethylamino-2-dimethyl-1-benzoyloxypropane.