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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404570Generated: October 31, 2026

Azane;hydrate → HCID 178474353, compound

https://huagongshe.com/reaction/2404570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzane;hydrateHCID 12896473—
ReactantHCID 68488136HCID 68488136—
SolventEthanolHCID 702—
ProductHCID 178474353HCID 17847435391.7%

Reaction Steps

10.6 g of 5-amino-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-3-hydroxypyrazole was dissolved in 200 mL of toluene, and to this solution, 20.0 g of acetyl chloride was added, followed by reflux with heating for 12 hours. After cooling to room temperature, the solvent was distilled off under reduced pressure, and the obtained residue was purified by column chromatography (developing solvent ethyl acetate:hexane=1:4) to obtain 9.4 g of 3-acetoxy-5-(N,N-diacetylamino)-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}pyrazole. Then, 9.4 g of the obtained 3-acetoxy-5-(N,N-diacetylamino)-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}pyrazole was dissolved in 100 mL of ethanol, and 10 mL of a 25 mass % ammonia water was added, followed by stirring at room temperature for 30minutes. Then, the solvent was distilled off under reduced pressure, and the obtained solid was washed with diisopropyl ether to obtain 7.0 g of 5-acetylamino-1-{2-fluoro-4-methyl-5-(2,2,2-trifluoroethylthio)phenyl}-3-hydroxypyrazole in the form of white crystals (melting point: 223-225° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802713B2
Source datasetuspto-grants-2014_08
ORD IDord-a8301ba9b42d49c399cfa14996b93d3b
Source noteuspto-grants-2014_08