Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622334Generated: October 30, 2026

Lawesson's reagent → 1-(3,5-Dichloropyridin-4-yl)piperidine-4-carbothioamide

https://huagongshe.com/reaction/1622334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3,5-Dichloropyridin-4-yl)piperidine-4-carboxamideHCID 2811640—
SolventTetrahydrofuranHCID 8028—
Product1-(3,5-Dichloropyridin-4-yl)piperidine-4-carbothioamideHCID 5837827948.2%

Reaction Steps

To a solution of 1-(3,5-dichloropyridin-4-yl)piperidine-4-carboxamide 23 (40 mg, 0.15 mmol) in THF (2 mL) was added Lawesson's reagent (71 mg, 0.18 mmol) and the mixture was heated at reflux for 2.5 h. After cooling to r.t. the mixture was poured into a saturated solution of sodium hydrogen carbonate (20 mL) and extracted with EtOAc (2×20 mL). The combined organic extracts were washed with water (20 mL), brine (20 mL), dried (MgSO4) and concentrated under reduced pressure. The crude product was purified by flash column chromatography on silica gel (CH2Cl2, MeOH, 99:1) to furnish the title compound as a white solid (21 mg, 40%), m/z (ESI) C11H14Cl2N2S requires 290.0280 found [M+H]+ 290.0280.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778925B2
Source datasetuspto-grants-2014_07
ORD IDord-9e630f9adb764fdf83f891e3dbcde354
Source noteuspto-grants-2014_07