Reaction #4001
ord-cb342278cc67421d861b38254858d7ca
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1Temperatureheated under nitrogen
- 2Otherpurge as the bath temperature
- 3Otherapproached 100° C.
- 4Otherreaction
- 5OtherWhen the initial reaction
- 6workup.WAITsubsided after a few minutes
- 7Temperaturethe bath temperature was raised to 130° C.
- 8Otheras indicated by cessation of gassing (about 1 hour)
- 9Temperatureto cool about 60° C.
- 10ExtractionThe solution was extracted with 500 parts of ethyl acetate
- 11workup.ADDITIONThe aqueous phase was treated with decolourising charcoal
- 12Filtrationfiltered
- 13workup.ADDITIONthe pH was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate solution
- 14FiltrationThe precipitated solid was filtered
- 15Washwashed with water
- 16Otherdried to constant weight at 80° C. in a vacuum oven
Procedure
620 parts of 4-chloro-4-chloromethyloxetan-2-one and 440 parts of guanidine hydrochloride were charged to a reaction flask and the mixture was stirred and heated under nitrogen purge as the bath temperature was gradually raised to 120° C. When the bath temperature approached 100° C., reaction commenced accompanied by evolution of hydrogen chloride. When the initial reaction subsided after a few minutes the bath temperature was raised to 130° C. and held until the reaction ceased as indicated by cessation of gassing (about 1 hour). The reaction mixture was allowed to cool about 60° C. and 1750 parts of water was added to the syrup. The solution was extracted with 500 parts of ethyl acetate and the extract was discarded. The aqueous phase was treated with decolourising charcoal, filtered and the pH was adjusted to pH 8 by the addition of saturated aqueous sodium bicarbonate solution. The precipitated solid was filtered, washed with water and dried to constant weight at 80° C. in a vacuum oven to give 2-amino-4-chloromethyl-6-hydroxypyrimidine, m.p. 195°-197° C.