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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880519Generated: November 2, 2026

Hydrogen Peroxide → Odanacatib

https://huagongshe.com/reaction/1880519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantEthyl AcetateHCID 8857—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 11496895HCID 11496895—
CatalystTetrabutylammonium hydrogen sulfateHCID 94433—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductOdanacatibHCID 10152654—

Reaction Steps

To a 0° solution of the sulfide (0.265 g) from Step 10 in toluene (5 mL) and dichloromethane (5 mL) was added Na2WO4.2H2O (0.002 g) and n-Bu4NHSO4 (0.01 g). 30% Hydrogen peroxide (0.137 mL) was then slowly added and the mixture was stirred at room temperature for 3 hours. The mixture was poured slowly onto a mixture of ice, dilute aqueous sodium thiosulfate and ethyl acetate. The organic layer was separated and the aqueous further extracted with ethyl acetate. The combined organic layers were washed with brine, dried with magnesium sulfate and the solvent was removed in vacuo to yield a residue which was purified on SiO2 using ethyl acetate, hexanes and dichloromethane (1:1:0.1) as eluant. The residue was triturated in diethyl ether to yield N1-(1-cyanocyclopropyl)-4-fluoro-N2-{(1S)-2,2,2-trifluoro-1-[4′-(methyl sulfonyl)-1,1′-biphenyl-4-yl]ethyl}-L-leucinamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318748B2
Source datasetuspto-grants-2012_11
ORD IDord-b9c434d925294a4b8a201f0460de8fdf
Source noteuspto-grants-2012_11