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HRID 3911作成日:2026年10月23日

Cesium fluoride → 2-Amino-4-fluoromethyl-6-methoxypyrimidine

https://huagongshe.com/ja/reaction/3911

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物4-(Chloromethyl)-6-methoxypyrimidin-2-amineHCID 13884815—
溶媒DimethylformamideHCID 6228—
生成物2-Amino-4-fluoromethyl-6-methoxypyrimidineHCID 20153497—

反応手順

A mixture of 17.0 parts of 2-amino-4-chloromethyl-6-methoxypyrimidine, 59.5 parts of caesium fluoride and 130 parts of dry dimethylformamide was stirred under reflux for 2 hours. The mixture was cooled and evaporated in vacuo. The residue was taken up in ethyl acetate and the solution was washed four times with water. The organic phase was dried with anhydrous magnesium sulphate, stirred with decolourising charcoal, filtered and evaporated. The crude product was purified by chromatography on silica, eluted with ethyl acetate to give 2-amino-4-fluoromethyl-6-methoxypyrimidine m.p. 119°-121° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723006
出典データセットuspto-grants-1988_02
ORD IDord-57c87955e9ed4a11aa4e6f98c7716c2b
出典メモuspto-grants-1988_02