CH207654A - Process for producing a pyrimidine compound. - Google Patents
Process for producing a pyrimidine compound.Info
- Publication number
- CH207654A CH207654A CH207654DA CH207654A CH 207654 A CH207654 A CH 207654A CH 207654D A CH207654D A CH 207654DA CH 207654 A CH207654 A CH 207654A
- Authority
- CH
- Switzerland
- Prior art keywords
- ethyl
- pyrimidine compound
- producing
- amino
- brominating agent
- Prior art date
Links
Landscapes
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Herstellung einer Pyrimidinverbindung. Gegenstand des vorliegenden Patentes ist ein Verfahren zur Herstellung einer Pyri- midinverbindung, welches dadurch gekenn zeichnet ist, dass man 2-Äthyl-4-amino-5-oxy- methylpyrimidindurch Einwirken eines Bromierungsmitteells in das 2-Äthyl-4-amino- 5-bro:
mmethyl-pyrimidin-hydrobromid um wandelt. Als Bromierungsmittel wird vor zugsweise Bromwasserstoffs!ure verwendet. Die so erhältliche Verbindung bildet Kri stalle vom 8ehmelzpunkt <B>197'.</B> Sie soll als Ausgangsstoff für chemische Synthesen ver- wendet werden.
<I>Beispiel:</I> 20 g 2-Äthyl-4-amino-5-oxymethyIpyri- midin werden in 3-00 cm' Eisessig gelöst, in die Lösung wird Bromwasserstoff eingeleitet. Dabei steigt die Temperatur bis gegen<B>60'.</B> Das erst ausgeschiedene Hydrobromid. des Alkohols .geht in Lösung, und nach und nach scheidet sich .das Hydrobromid,des 2-Äthyl- 4-a:mino-5-brommethyl-pyrimidins in feinen Kristallen ab.
Diese werden abgesaugt und mit Eisessig und mit Äther :gewaschen. F.<B>197'</B> unter Zersetzung.
Da--selbe Produkt erhält man beim Er wärmen von 2-Äthyl-4-amino-5-oxymethyl- pyrimidin mit wässriger Bromwasserstoff- säure (d 1,7) auf dem Wasserbad.
Process for producing a pyrimidine compound. The subject of the present patent is a process for the preparation of a pyrimidine compound, which is characterized in that 2-ethyl-4-amino-5-oxymethylpyrimidine is added to the 2-ethyl-4-amino-5- by the action of a brominating agent. bro:
converts mmethyl-pyrimidine-hydrobromide. Hydrogen bromic acid is preferably used as the brominating agent. The compound obtainable in this way forms crystals with a melting point <B> 197 '. </B> It is intended to be used as a starting material for chemical syntheses.
<I> Example: </I> 20 g of 2-ethyl-4-amino-5-oxymethyIpyrimidine are dissolved in 3-00 cm 'glacial acetic acid, and hydrogen bromide is passed into the solution. The temperature rises to about <B> 60 '. </B> The hydrobromide that is first separated out. of the alcohol. goes into solution, and gradually. The hydrobromide, the 2-ethyl-4-a: mino-5-bromomethyl-pyrimidine separates in fine crystals.
These are sucked off and washed with glacial acetic acid and with ether. F. <B> 197 '</B> with decomposition.
The same product is obtained when 2-ethyl-4-amino-5-oxymethylpyrimidine is heated with aqueous hydrobromic acid (d 1.7) on a water bath.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE207654X | 1936-05-15 | ||
CH205894T | 1937-04-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH207654A true CH207654A (en) | 1939-11-15 |
Family
ID=25724227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH207654D CH207654A (en) | 1936-05-15 | 1937-04-27 | Process for producing a pyrimidine compound. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH207654A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5136896A (en) * | 1990-11-26 | 1992-08-11 | Versa Tech Engineering | Rotary indexing apparatus |
-
1937
- 1937-04-27 CH CH207654D patent/CH207654A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5136896A (en) * | 1990-11-26 | 1992-08-11 | Versa Tech Engineering | Rotary indexing apparatus |
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