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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450149Generated: October 28, 2026

Methanol → HCID 19975240, compound

https://huagongshe.com/reaction/1450149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 19975239HCID 19975239—
SolventAcetonitrileHCID 6342—
ProductHCID 19975240HCID 19975240—

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 0.42 g (0.92 mmol) of N-(2,6-dichlorophenyl)-5-bromo-8-chloro[1,2,4]triazolo[1,5-a]-pyrazine-2-sulfonamide in 30 mL of dry acetonitrile was combined with 2.8 mL (5.6 mmol) of a 2M solution of sodium methoxide in methanol and the mixture was warmed to 40° C. under a nitrogen atmosphere with stirring. After 24 hours, the reaction was quenched with 1 mL of glacial acetic acid and the solvent was removed under reduced pressure. The residue was extracted portionwise with up to 100mL of tetrahydrofuran and the cloudy extract obtained was filtered and concentrated by evaporation under reduced pressure. The title compound was isolated from the residue obtained by flash column chromatography on silica gel using a 2 to 10 percent ethanol/dichloromethane gradient as eluent. The title compound, which was the least polar of the three compounds present, was further purified by extraction with warm methanol and diethyl ether mixtures to obtain 46 mg (12 percent of theory) as a white powder melting above 250° C. with decomposition.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602075
Source datasetuspto-grants-1997_02
ORD IDord-8bf524052c9a416c9dd7af14018fc1ae
Source noteuspto-grants-1997_02