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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244584Generated: October 25, 2026

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

https://huagongshe.com/reaction/244584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTrifluoroiodomethaneHCID 16843—
Reactant2-Amino-5-bromopyrazineHCID 599539—
CatalystBis(eta-cyclopentadienyl) ironHCID 7611—
SolventDimethyl SulfoxideHCID 679—
SolventSodium chloride; waterHCID 57417360—
Product5-Bromo-3-(trifluoromethyl)pyrazin-2-amineHCID 7174135928.9%

Reaction Conditions

Temperature50 °C

Reaction Steps

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)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658661B2
Source datasetuspto-grants-2014_02
ORD IDord-502cb32e004d458eacc41558af5f2121
Source noteuspto-grants-2014_02