Reaktion #522728
ord-73ea23cf65e94a7f8c316530d1bc0214
Reaktionsgleichung
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeequipped with a mechanical stirrer
- 2Temperaturthermometer and reflux condenser
- 3workup.ADDITIONAfter the addition
- 4Temperaturthe reaction mixture is heated
- 5Temperaturat reflux
- 6workup.STIRRINGwith continued stirring for a period of about 30 minutes
- 7FiltrationAfter this time the reaction mixture is filtered
Vorschrift
Tetrahydro-1-(5-t-butyl-1,3,4-thiadiazol-2-yl)-3 -methyl-6-hydroxy-2(1H)-pyrimidinone (0.05 mole), triethylamine (0.06 mole) and benzene (50 ml) are charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. 4-Methoxybenzoyl chloride (0.05 mole) is then added dropwise with stirring. After the addition is completed, the reaction mixture is heated at reflux with continued stirring for a period of about 30 minutes. After this time the reaction mixture is filtered and the filtrate is stripped of solvent under reduced pressure to yield the desired product tetrahydro-1-(5-t-butyl-1,3,4 -thiadiazol-2-yl)-3-methyl-6-(4-methoxybenzoyloxy)-2(1 H)-pyrimidinone.