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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291228Generated: October 30, 2026

Pyridine → HCID 19856564, compound

https://huagongshe.com/reaction/2291228

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantHCID 178493752HCID 178493752—
SolventDichloromethaneHCID 6344—
ProductHCID 19856564HCID 1985656468.6%

Reaction Steps

62 g of trifluoromethanesulfonic acid anhydride are added dropwise to a suspension of 31.2 g of 3-hydroxy-5-methoxy-1-methylpyrazin-2-one, 15.8 g of pyridine and 500 ml of methylene chloride at 20°-25° C. The solution formed is stirred at 20°-25° C. for a further 2 hours, and 200 ml of ice-water are then added. The organic phase is separated off, washed with 10% sodium bicarbonate solution and water, dried over sodium sulfate and evaporated to give 39.5 g of 5-methoxy-1-methyl-3-trifluoromethylsulfonyloxy-pyrazin-2-one of melting point 107°-108° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04795486
Source datasetuspto-grants-1989_01
ORD IDord-5e59a9a094434250a4df112987f378eb
Source noteuspto-grants-1989_01