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DE325156C - Process for the preparation of a double compound from quinine - Google Patents

Process for the preparation of a double compound from quinine

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Publication number
DE325156C
DE325156C DE1918325156D DE325156DD DE325156C DE 325156 C DE325156 C DE 325156C DE 1918325156 D DE1918325156 D DE 1918325156D DE 325156D D DE325156D D DE 325156DD DE 325156 C DE325156 C DE 325156C
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DE
Germany
Prior art keywords
quinine
double compound
preparation
alcoholic
alcohol
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
DE1918325156D
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German (de)
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Individual
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Individual
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Publication date
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Publication of DE325156C publication Critical patent/DE325156C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D453/00Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
    • C07D453/02Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
    • C07D453/04Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems having a quinolyl-4, a substituted quinolyl-4 or a alkylenedioxy-quinolyl-4 radical linked through only one carbon atom, attached in position 2, e.g. quinine

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

Description

Verfahren zur Herstellung einer Doppelverbindung aus Chinin. Die Erfindung betrifft ein Verfahren zur Irerstellung einer therapeutisch wertvollen Chinindoppelverbindung und besteht darin, daß Chinin und Hexamethylentetramin an Weinsäure gebunden werden. Die einzelnen Komponenten werden in äquimolelcularem @'erhältnis und unter solchen Bedingungen zusammengebracht, daß sich die neue Doppelverbindung als unlöslicher Niederschlag abscheidet. Zu diesem Zwecke bereitet man eine alkoholische Lösung der beiden Basen und gießt in sie eine ebenfalls alkoholische Weinsäurelösung, saugt nach einiger Zeit den Liederschlag ab, der gewaschen und getrocknet wird. Das Filtrat kann wieder als Lösungsmittel dienen. Anstatt von Chinin kann man auch von Chininsalzen ausgehen, die mit alkoholischer Lauge zersetzt werden.Process for the preparation of a double compound from quinine. The invention relates to a method for preparing a therapeutically valuable quinine double compound and consists in that quinine and hexamethylenetetramine are bound to tartaric acid. The individual components are in equimolelcularem @ 'and under such Conditions brought together that the new double compound is more insoluble Precipitation separates. For this purpose an alcoholic solution is prepared of the two bases and pours an alcoholic tartaric acid solution into them, sucks after a while, the song blows off, which is washed and dried. The filtrate can again serve as a solvent. Instead of quinine you can also use quinine salts that are decomposed with alcoholic lye.

Die Hauptvorteile der neuen Verbindung bestehen in dem fast vollständigen Fehlen, des bitteren Nachgeschmackes, ferner darin, daß sie keinen Chininrausch hervorruft, und schließlich darin, daß gleich große Gaben des nur ungefähr 6o Prozent Chinin enthaltenden Mittels die gleiche entfiebernde Wirkung wie reines Chinin zeigen. Außerdem scheint in hartnäckigen Fieberfällen bessere Wirkung als mit Chinin zti erzielen sein, und (las Mittel scheint sich auch dbrt zti bewähren, wo bisher Hexamethylentetramin verwendet wurde, Beispiel. a1 i 1'1n1. reines Chinin und i hfol. Hexanietliwlentetraniin \verden mit ungefähr 1 1 hochgradigem Alkohol übergossen und durch 1.2 bis 24 Stunden langes Stehen und Umrühren gelöst. Gleichzeitig wird getrennt i Mol. feingepulverte Weinsäure in i5o ccin Alkohol ebenfalls durch längeres Stehen gelöst. Wenn beide Lösungen fertig sind, gießt man die Säurelösung langsam unter gutem Rühren in die Lösung der Basen, läßt kurze Zeit stehen und saugt dann die abgeschiedene Doppelverbindung ab. Man wäscht zuerst mit Alkohol, dann mit Äther und trocknet scharf und schnell im Vakuum, gegebenenfalls unter Erwärmen auf höchstens 45'_C und Anwendunevon Phosphorpentoxyd. Das Filtrat kann ohne weiteres als Lösungsmittel wieder verwendet werden. Schließlich kann in .m für Hexamethylentetramin und Weinsäure auch Wasser als Lösungsmittel benutzen, doch ist das Filtrat dann nicht weiter brauchbar, und man tut gut, in diesem Falle mit 1,05 -bis r, i Mol. HexametliyIentetramin zu arbeiten.The main advantages of the new compound are the almost complete absence of the bitter aftertaste, the fact that it does not induce a quinine intoxication, and finally that equal doses of the agent, which contains only about 60 percent quinine, have the same defensive effect as pure quinine. In addition, in persistent fever cases a better effect appears to be achieved than with quinine, and (the remedy also seems to prove itself in cases where hexamethylenetetramine has been used up to now, for example 1 liter of high-grade alcohol is poured over it and dissolved by standing for 1.2 to 24 hours and stirring. At the same time, 1 mol. Of finely powdered tartaric acid is dissolved separately in 150 cc of alcohol, also by standing for a long time. When both solutions are ready, the acid solution is slowly poured into it with thorough stirring the solution of the bases is allowed to stand for a short time and then the separated double compound is filtered off with suction. It is washed first with alcohol, then with ether and dried sharply and quickly in vacuo, if necessary with heating to a maximum of 45 ° C. and application of phosphorus pentoxide. The filtrate can be used without can also be reused as a solvent. Finally, in .m for hexamethylenetetramine and white acid can also use water as a solvent, but the filtrate is then no longer usable, and in this case it is a good idea to work with 1.05 to r.1 mol of hexamethylene tetramine.

b) Geht man nicht von Chinin, sondern von einem Chininsalz aus, so ,wird die b°rechnete Menge Ätznatron in i Teil Alkohol gelöst und i Teil eines Chininsalzes allmählich unter Rühren eingetragen. Sobald im Bodensatz keine gallertigen Teilchen mehr erkennbar sind, wird scharf abgesaugt und mit Alkohol gewaschen. Mit dieser Chininlösung wird nach a «-eitergearbeitet.b) If one does not proceed from quinine, but from a quinine salt, then , the calculated amount of caustic soda is dissolved in 1 part of alcohol and 1 part of a quinine salt gradually entered with stirring. As soon as there are no gelatinous particles in the sediment more are recognizable, is sharply suctioned off and washed with alcohol. With this Quinine solution is worked on according to a «.

Die neue Chinindoppelverbindung ist ein weißer, in Wasser und Alkohol fast unlöslicher Körper, läßt sich aus heißem Wasser in langen Nadeln unikristallisieren und zersetzt sich vor dem Schmelzen. Ihr Geschmack ist säuerlich-bitter; der dem Chinin eigene Nachgeschmack fehlt.The new quinine double compound is a white one, in water and alcohol almost insoluble body, can be unicrystallized from hot water in long needles and decomposed before melting. Their taste is sour-bitter; which lacks the aftertaste inherent in quinine.

Claims (1)

PATENT-ANSPRUCH: Verfahren zur Herstellung einer Doppelverbindung- aus Chinin, darin bestehend, daß man Chinin oder die äquivalente Menge eines Chininsalzes und einer Base, wie z. B. Alkalihydroxy d, Weinsäure und Hexamethylentetramin in äduimolekularen Mengen in alkoholischer oder wäßrig-alkoholisclier Lösung, aufeinander einwirken läßt und die so entstandene Doppelverbindung nach den üblichen Methoden abscheidet.PATENT CLAIM: Process for the production of a double connection of quinine, consisting of adding quinine or the equivalent amount of a quinine salt and a base such as B. alkali hydroxide, tartaric acid and hexamethylenetetramine in Aduimolecular amounts in alcoholic or aqueous-alcoholic solution, one on top of the other can act and the resulting double compound by the usual methods separates.
DE1918325156D 1918-11-22 1918-11-22 Process for the preparation of a double compound from quinine Expired DE325156C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE325156T 1918-11-22

Publications (1)

Publication Number Publication Date
DE325156C true DE325156C (en) 1920-09-08

Family

ID=6182614

Family Applications (1)

Application Number Title Priority Date Filing Date
DE1918325156D Expired DE325156C (en) 1918-11-22 1918-11-22 Process for the preparation of a double compound from quinine

Country Status (1)

Country Link
DE (1) DE325156C (en)

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