Reaktionsgleichung
[NH2:1][C:2]1[N:7]=[C:6](F)[CH:5]=[C:4]([CH2:9][F:10])[N:3]=1.C(O)(=[O:13])C>>[NH2:1][C:2]1[NH:7][C:6](=[O:13])[CH:5]=[C:4]([CH2:9][F:10])[N:3]=1Komponenten
3
Versuchsvorschrift
12.1 Parts of 2-amino-4-fluoro-6-fluoromethylpyrimidine was dissolved in 200 parts of 20% aqueous acetic acid at reflux, with stirring. The mixture was heated under reflux for 1 hour then cooled. The precipitated solid was filtered, washed with 50% aqueous acetic acid and then with acetone. The solid was dried in vacuo at 140° C. to give 2-amino-6-fluoromethylpyrimidine-4-one, m.p. 237°-238° C. (decomposition).
Aufarbeitung
- temperatureat reflux
- temperatureThe mixture was heated
- temperatureunder reflux for 1 hour
- temperaturethen cooled
- filtrationThe precipitated solid was filtered
- washwashed with 50% aqueous acetic acid
- customThe solid was dried in vacuo at 140° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-f197a439b25842d9882c6684168e87b0
- Quelldatensatz
- uspto-grants-1988_02
- Patentnummer
- US04723006
Verknüpfte Notizen
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