CH269982A - Process for the preparation of a derivative of 3,5-dioxo-pyrazolidine. - Google Patents

Process for the preparation of a derivative of 3,5-dioxo-pyrazolidine.

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Publication number
CH269982A
CH269982A CH269982DA CH269982A CH 269982 A CH269982 A CH 269982A CH 269982D A CH269982D A CH 269982DA CH 269982 A CH269982 A CH 269982A
Authority
CH
Switzerland
Prior art keywords
dioxo
pyrazolidine
derivative
preparation
diphenyl
Prior art date
Application number
Other languages
German (de)
Inventor
Ag J R Geigy
Original Assignee
Ag J R Geigy
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 Ag J R Geigy filed Critical Ag J R Geigy
Publication of CH269982A publication Critical patent/CH269982A/en

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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

  

  <B>Verfahren zur Herstellung eines Derivates des</B>     3,5-Dioxo-pyrazolidins.       Gegenstand vorliegenden Patentes ist ein  Verfahren zur Herstellung eines Derivates des       3,5-Dioxo-pyrazolidins.    Das Verfahren ist da  durch gekennzeichnet, dass man     1,2-Diphenyl-          3,5-dioxo-pyrazolidin,        Benzaldehyd    und ein  hydrierendes Mittel aufeinander einwirken  lässt.  



  Die erhaltene neue Verbindung, das     1,2-Di-          phenyl-3,5-dioxo-4-benzyl-pyrazolidin,    zeigt  einen Schmelzpunkt von 136-138 . Sie soll  therapeutische Verwendung finden.  



  <I>Beispiel:</I>  Eine Lösung von 160 Teilen     1,2-Diphenyl-          3,5-dioxo-pyrazolidin    und 120 Teilen Benz  aldehyd in 500     Volumteilen    Alkohol wird  unter 20 Atmosphären     @Vasserst@offdruck    bei  Gegenwart von     Raney-Nickel    auf 100  erhitzt,  bis die Wasserstoffaufnahme langsam und die  Lösung farblos wird. Aus der heiss filtrierten  Lösung kristallisiert das     1,2-Diphenyl-3,5-          dioxo-4-benzyl-pyrazolidin    vom Schmelzpunkt  136 bis 138<B>0</B> aus.



  <B> Process for the preparation of a derivative of </B> 3,5-dioxo-pyrazolidine. The present patent relates to a process for the preparation of a derivative of 3,5-dioxo-pyrazolidine. The process is characterized in that 1,2-diphenyl-3,5-dioxo-pyrazolidine, benzaldehyde and a hydrogenating agent are allowed to act on one another.



  The new compound obtained, 1,2-diphenyl-3,5-dioxo-4-benzylpyrazolidine, has a melting point of 136-138. It should find therapeutic use.



  <I> Example: </I> A solution of 160 parts of 1,2-diphenyl-3,5-dioxo-pyrazolidine and 120 parts of benzaldehyde in 500 parts by volume of alcohol is under 20 atmospheres @ Vasserst @ off pressure in the presence of Raney nickel heated to 100 until the hydrogen uptake slowly and the solution becomes colorless. The 1,2-diphenyl-3,5-dioxo-4-benzyl-pyrazolidine with a melting point of 136 to 138 crystallizes out of the hot-filtered solution.

 

Claims (1)

PATENTANSPRUCH: Verfahren zur Herstellung eines Derivates des 3,5-Dioxopyrazolidins, dadurch gekenn zeichnet, dass man 1,2-Diphenyl-3,5-dioxo-pyr- azolidin, Benzaldehyd und ein hydrierendes Mittel aufeinander einwirken lässt. Die erhaltene neue Verbindung, das 1,2-Di- phenyl-3,5-dioxo-4-benzyl-pyrazolidin, zeigt einen Schmelzpunkt von 136-138 . UN TERANSPRL CHE 1. Verfahren nach Patentanspruch, da durch gekennzeichnet., dass man als hydrieren des Mittel Wasserstoff in Gegenwart. eines HydrierungskatalyBators verwendet. 2. PATENT CLAIM: Process for the preparation of a derivative of 3,5-dioxopyrazolidine, characterized in that 1,2-diphenyl-3,5-dioxo-pyrazolidine, benzaldehyde and a hydrogenating agent are allowed to act on one another. The new compound obtained, 1,2-diphenyl-3,5-dioxo-4-benzylpyrazolidine, has a melting point of 136-138. UN TERANSPRL CHE 1. Process according to claim, characterized in that the hydrogenation of the agent is hydrogen in the presence. a hydrogenation catalyst is used. 2. Verfahren nach Patentanspruch und Unteranspruch 1, dadurch gekennzeichnet, dass man das 1,2-Diphenyl-3,5-dioxo-pyrazol- idin, den Benzaldehyd und den Wasserstoff <B>01</B> eichzeitig aufeinander einwirken lässt. Process according to claim and dependent claim 1, characterized in that the 1,2-diphenyl-3,5-dioxo-pyrazolidine, the benzaldehyde and the hydrogen 01 are allowed to act on one another at the same time.
CH269982D 1948-03-22 1948-03-22 Process for the preparation of a derivative of 3,5-dioxo-pyrazolidine. CH269982A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH269982T 1948-03-22
CH266237T 1948-03-22

Publications (1)

Publication Number Publication Date
CH269982A true CH269982A (en) 1950-07-31

Family

ID=25730856

Family Applications (1)

Application Number Title Priority Date Filing Date
CH269982D CH269982A (en) 1948-03-22 1948-03-22 Process for the preparation of a derivative of 3,5-dioxo-pyrazolidine.

Country Status (1)

Country Link
CH (1) CH269982A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2909465A (en) * 1952-09-18 1959-10-20 Knoll Ag 1, 4-diphenyl-3, 5-diketo pyrazolidine compounds and compositions

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2909465A (en) * 1952-09-18 1959-10-20 Knoll Ag 1, 4-diphenyl-3, 5-diketo pyrazolidine compounds and compositions

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