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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409541Generated: November 1, 2026

Sodium Thiosulfate → HCID 67272364, compound

https://huagongshe.com/reaction/1409541

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 67272916HCID 67272916—
SolventDichloromethaneHCID 6344—
ProductHCID 67272364HCID 6727236491%

Reaction Steps

To a solution of 6-(2-chlorophenyl)-3-ethoxycarbonyl-7-(4-trifluoromethyl-phenyl)-2-methylthiopyrazolo[1,5-a]pyrimidine (compound obtained in Reference Example A5; 11.0 g) in methylene chloride (400 mL) was added m-chloroperbenzoic acid (16.5 g) at 0° C., and the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added dropwise an aqueous sodium thiosulfate solution at 0° C. under stirring, and the mixture was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated in vacuo, and the resultant crude product was washed with ethanol to give 6-(2-chlorophenyl)-3-ethoxycarbonyl-7-(4-trifluoromethylphenyl)-2-methylsulfonylpyrazolo[1,5-a]pyrimidine (10.7 g, yield: 91%) as a powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921380B2
Source datasetuspto-grants-2014_12
ORD IDord-669031bee9f546cc9483b4272b0317eb
Source noteuspto-grants-2014_12