戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 244584作成日:2026年10月25日

Hydrogen Peroxide → 5-Bromo-3-(trifluoromethyl)pyrazin-2-amine

https://huagongshe.com/reaction/244584

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen PeroxideHCID 784—
反応物TrifluoroiodomethaneHCID 16843—
反応物2-Amino-5-bromopyrazineHCID 599539—
触媒Bis(eta-cyclopentadienyl) ironHCID 7611—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Sodium chloride; waterHCID 57417360—
生成物5-Bromo-3-(trifluoromethyl)pyrazin-2-amineHCID 7174135928.9%

反応条件

温度50 °C

反応手順

To a solution of 2-amino-5-bromopyrazine (174 mg, 1 mmol) in DMSO (3 ml) stifling under Ar is added ferrocene (56 mg, 0.3 mmol) and degassed for 5 minutes with Ar. 2 ml of 1N H2SO4 in DMSO is added, followed by CF3I (0.276 ml, 3 mmol) in DMSO (2 ml), giving a slight yellow solution. 0.2 ml of 30% H2O2 is added slowly, causing the reaction to go from yellow to dark green in color. The reaction was heated to 50° C. for 2 hours under Ar. After cooling to room temperature, the reaction mixture is poured into brine, and product is extracted with EtOAc (4×20 ml). The combined organic fractions are dried with magnesium sulfate, filtered, then concentrated in vacuo. The crude material was purified by flash chromatography (SiO2, Biotage SNAP 10 g, 0-50% EtOAc/hept) which yields 70 mg of title compound; m/z 242.0, 244.0 (M, M+2H)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658661B2
出典データセットuspto-grants-2014_02
ORD IDord-502cb32e004d458eacc41558af5f2121
出典メモuspto-grants-2014_02