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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3905Generated: October 24, 2026

Hydrochloric Acid → 2-amino-6-(chloromethyl)-1H-pyrimidin-4-one

https://huagongshe.com/en/reaction/3905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantGuanidine HydrochlorideHCID 5742—
Reactant4-Chloro-4-(chloromethyl)oxetan-2-oneHCID 13718281—
SolventWaterHCID 962—
Product2-amino-6-(chloromethyl)-1H-pyrimidin-4-oneHCID 178418565—

Reaction Conditions

Temperature120 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04723006
Source datasetuspto-grants-1988_02
ORD IDord-cb342278cc67421d861b38254858d7ca
Source noteuspto-grants-1988_02