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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228160Generated: October 31, 2026

Sodium Thiosulfate → HCID 18472221, compound

https://huagongshe.com/reaction/2228160

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 18472585HCID 18472585—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18472221HCID 1847222141.6%

Reaction Steps

To a solution of N-[4-[hydroxy(2-pyridyl)methyl]-phenyl]-6—(4-methylphenyl)-2-methyl-2H-1-benzopyran-3-carboxamide (300 mg) in tetrahydrofuran (10 ml) was added 3-chloroperbenzoic acid (70%, 0.24 g) at 0° C., and the mixture was stirred at room temperature for 24 hours. To the mixture was add ed sodium thiosulfate, and the mixture was stirred for a few minutes. was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate solution and saturated sodium chloride solution, dried with agnesium sulfate and concentrated. The residue was separated and purified with column chromatography (ethanol/ethyl acetate=1:2) to give crystals, which were recrystallized from ethanol-ethyl acetate to give N-[4-[hydroxy(1-oxidopyridin-2-yl)-methyl]phenyl]-6—(4-methylphenyl)-2-methyl-2H-1-benzopyran-3-carboxamide (Compound 203) (129 mg) as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413947B1
Source datasetuspto-grants-2002_07
ORD IDord-3ccd2b07c26640e896780bb03ff00d4f
Source noteuspto-grants-2002_07