AT34249B - Process for the preparation of 2.4.6-trioxypyrimidine and its 5-mono- and dialkyl derivatives. - Google Patents

Process for the preparation of 2.4.6-trioxypyrimidine and its 5-mono- and dialkyl derivatives.

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Publication number
AT34249B
AT34249B AT34249DA AT34249B AT 34249 B AT34249 B AT 34249B AT 34249D A AT34249D A AT 34249DA AT 34249 B AT34249 B AT 34249B
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AT
Austria
Prior art keywords
trioxypyrimidine
mono
preparation
acid
dialkyl derivatives
Prior art date
Application number
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German (de)
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Boehringer & Soehne
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.)
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Publication date
Application filed by Boehringer & Soehne filed Critical Boehringer & Soehne
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Publication of AT34249B publication Critical patent/AT34249B/en

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Description

  

   <Desc/Clms Page number 1> 
 



    Verfahren zur Darstellung von 2.4.6-Trioxypyrimidin und dessen 5-Mono-und Dialkylderivaten.   
 EMI1.1 
 
 EMI1.2 
 
 EMI1.3 
 2.4.   6-Trioxypyrimidin     (Barbitursäure) bzw.   dessen 5-Mono- und Dialkylderivate überzugehen. Es bietet sich hiedurch ein neuer Weg zur Darstellung dieser therapeutisch wertvollen Verbindungen. 



   Beispiel I : Darstellung von 2. 4.6-Trioxypyrimidin (Barbitursäure). Das als Ausgangsmaterial dienende Malonestersäureureid 
 EMI1.4 
 wird durch Einwirkung von Malonestersäurechlorid (Kp.   71    bei 15 mm) auf mindestens 2 Mol. Harnstoff und Trennung des Reaktionsgemisches mit Wasser erhalten. Das Ureid 
 EMI1.5 
 es setzt sich schwerlösliches, barbitursaures Natrium zu Boden, das mit Salzsäure reine Barbitursäure ergibt. 



   Beispiel II : Darstellung von 5-Monoäthyl-2. 4. 6-Trioxypyrimidin (Äthylbarbitursäure). 



  Das hiebei benutzte Äthylmalonestersäureureid 
 EMI1.6 
 
 EMI1.7 
 

 <Desc/Clms Page number 2> 

 
 EMI2.1 
 Die Löslichkeit in Wasser ist gering.   I.   2,2 kg Diäthylmalonäthylestersäureureid werden mit 20 l konzentriertem wässrigen Ammoniak bei   gewöhnlicher Temperatur   gut durchmischt. Nach 1 Stunde ist eine Lösung entstanden, die nach Abdunsten des überschüssigen Ammoniaks und 
 EMI2.2 
 und man kann mittels Salzsäure 1,7 kg reine   Diäthylbarbitursäure   ausfällen.



   <Desc / Clms Page number 1>
 



    Process for the preparation of 2,4,6-trioxypyrimidine and its 5-mono- and dialkyl derivatives.
 EMI1.1
 
 EMI1.2
 
 EMI1.3
 2.4. 6-trioxypyrimidine (barbituric acid) or its 5-mono- and dialkyl derivatives. This offers a new way of representing these therapeutically valuable connections.



   Example I: Preparation of 2,4,6-trioxypyrimidine (barbituric acid). The malonic ester acid acid used as starting material
 EMI1.4
 is obtained by the action of malonic ester acid chloride (b.p. 71 at 15 mm) on at least 2 moles of urea and separation of the reaction mixture with water. The ureid
 EMI1.5
 sparingly soluble, barbituric acid sodium settles on the ground, which with hydrochloric acid results in pure barbituric acid.



   Example II: Preparation of 5-monoethyl-2. 4. 6-trioxypyrimidine (ethyl barbituric acid).



  The ethyl malonic ester acid ureid used here
 EMI1.6
 
 EMI1.7
 

 <Desc / Clms Page number 2>

 
 EMI2.1
 The solubility in water is low. I. 2.2 kg of diethyl malonic ester acid acid are mixed well with 20 l of concentrated aqueous ammonia at ordinary temperature. After 1 hour a solution has formed which, after the excess ammonia has evaporated, and
 EMI2.2
 and 1.7 kg of pure diethylbarbituric acid can be precipitated using hydrochloric acid.

 

Claims (1)

PATENT-ANSPRUCH : EMI2.3 derivaten, darin bestehend, dass man Estersäureureide der Malonsäure bzw. der Mono-oder Dialkylmalonsäuren der allgemeinen Formel : EMI2.4 EMI2.5 PATENT CLAIM: EMI2.3 derivatives, consisting in that one ester acid acid of malonic acid or of mono- or dialkylmalonic acids of the general formula: EMI2.4 EMI2.5
AT34249D 1907-02-13 1907-12-20 Process for the preparation of 2.4.6-trioxypyrimidine and its 5-mono- and dialkyl derivatives. AT34249B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE193447D 1907-02-13

Publications (1)

Publication Number Publication Date
AT34249B true AT34249B (en) 1908-09-10

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ID=5739142

Family Applications (1)

Application Number Title Priority Date Filing Date
AT34249D AT34249B (en) 1907-02-13 1907-12-20 Process for the preparation of 2.4.6-trioxypyrimidine and its 5-mono- and dialkyl derivatives.

Country Status (1)

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AT (1) AT34249B (en)

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