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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849951Generated: October 31, 2026

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

https://huagongshe.com/reaction/849951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(2,4-Dichloro-5-methoxyphenyl)-6-trifluoromethyl-2-oxo-1,2-dihydropyrazinHCID 19365518—
SolventDimethylformamideHCID 6228—
Product3-(2,4-Dichloro-5-methoxyphenyl)-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazineHCID 1936553148.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

First, 2.20 g of 3-(2,4-dichloro-5-methoxyphenyl)-6-trifluoromethyl-2-oxo-1,2-dihydropyrazin (compound 1-1009) was dissolved in 12 ml of N,N-dimethylformamide, to which 1.34 g of potassium carbonate and 0.81 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 1.11 g (yield, 48%) of 3-(2,4-dichloro-5-methoxyphenyl)-1-methyl-6-trifluoromethyl-2-oxo-1,2-dihydropyrazine (present compound 1-358; m.p., 130.6° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06015774
Source datasetuspto-grants-2000_01
ORD IDord-6d396bfe1c114f0bb3913f95de120d2e
Source noteuspto-grants-2000_01