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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849926Generated: October 30, 2026

Water → 3-(4-Chloro-2-fluoro-5-methoxyphenyl)-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazine

https://huagongshe.com/reaction/849926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(4-Chloro-2-fluoro-5-methoxyphenyl)-6-trifluoromethyl-2-oxo-1,2-dihydropyrazineHCID 15452079—
SolventDimethylformamideHCID 6228—
Product3-(4-Chloro-2-fluoro-5-methoxyphenyl)-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazineHCID 1545208055%

Reaction Conditions

Temperature100 °C

Reaction Steps

First, 3.61 g of 3-(4-chloro-2-fluoro-5-methoxyphenyl)-6-trifluoromethyl-2-oxo-1,2-dihydropyrazine (compound 1-1008) was dissolved in 16 ml of N,N-dimethylformamide, to which 2.35 g of potassium carbonate and 1.39 ml of methyl iodide were added, and the mixture was stirred at 100° C. for 2 days. After completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The organic layer was washed with saturated sodium chloride solution, dried with anhydrous magnesium sulfate, and concentrated. The residue was subjected to silica gel column chromatography (eluent, hexane/ethyl acetate=5:1), which afforded 2.04 g (yield, 55%) of 3-(4-chloro-2-fluoro-5-methoxyphenyl)-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazine (present compound 1-144; m.p., 108.7° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06015774
Source datasetuspto-grants-2000_01
ORD IDord-7477ba88d9fc4b13be517525aec5625d
Source noteuspto-grants-2000_01