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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1774544Generated: October 31, 2026

Sodium Thiosulfate → HCID 71612145, compound

https://huagongshe.com/reaction/1774544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 71611599HCID 71611599—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 71612145HCID 71612145—

Reaction Conditions

Temperature0 °C

Reaction Steps

180 mg 2-[5-cyclopropyl-1-(4-ethoxy-2,6-difluorobenzyl)-4-methyl-1H-pyrazol-3-yl]-5-[2-(methylsulfanyl)ethoxy]-N-(pyridin-4-yl)pyrimidin-4-amine (0.326 mmol, 1.0 eq.) were dissolved in 1.7 mL chloroform and cooled to 0° C. 80.3 mg 3-chlorobenzenecarboperoxoic acid and the reaction mixture was stirred at 0° C. for 30 minutes. The reaction mixture was diluted with DCM and a solution of sodium thiosulfate (10% in water) was added and stirred for 5 minutes. The layers were separated and the aqueous layer was washed with DCM twice. The combined organic layers were washed with saturated sodium hydrogencarbonate solution, was dried over a silicon filter and concentrated in vacuo. The crude product was purified by flash chromatography to provide 136 mg of the analytically pure target compound as a racemate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260412B2
Source datasetuspto-grants-2016_02
ORD IDord-733c52cec7c341479611775233ceff79
Source noteuspto-grants-2016_02