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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340165Generated: October 30, 2026

Water → tert-butyl[(3S,5S)-5-(2,3-difluorophenyl)-2-thioxopiperidin-3-yl]carbamate

https://huagongshe.com/reaction/340165

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLawesson's reagentHCID 87949—
ReactantSodium BicarbonateHCID 516892—
Reactanttert-butyl[(3S,5S)-5-(2,3-difluorophenyl)-2-oxopiperidin-3-yl]carbamateHCID 69096669—
SolventTolueneHCID 1140—
Producttert-butyl[(3S,5S)-5-(2,3-difluorophenyl)-2-thioxopiperidin-3-yl]carbamateHCID 86698227140.4%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of tert-butyl [(3S,5S)-5-(2,3-difluorophenyl)-2-oxopiperidin-3-yl]carbamate (300 mg, 0.92 mmol) in toluene (9.2 mL) was added Lawesson's Reagent (190 mg, 0.47 mmol). The mixture was stirred at 40° C. After 16 h, the mixture was cooled to ambient temperature and saturated aqueous sodium bicarbonate was added. Water was added, and the mixture was extracted with ethyl acetate (3×). The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered and concentrated. Purification by reverse phase chromatography (C-18, 90% water/acetonitrile→5% water/acetonitrile with 0.1% trifluoroacetic acid) gave the title compound (226 mg). MS 365.3 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895572B2
Source datasetuspto-grants-2014_11
ORD IDord-9c7241c5eb284a1294ffbbc4e32f1a14
Source noteuspto-grants-2014_11