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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408329Generated: November 4, 2026

Lawesson's reagent → 1,1-Dimethylethyl 4-(aminocarbonothioyl)-4-methyl-1-piperidinecarboxylate

https://huagongshe.com/reaction/1408329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant1-Boc-4-methylpiperidine-4-carboxamideHCID 53393793—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 4-(aminocarbonothioyl)-4-methyl-1-piperidinecarboxylateHCID 57473378—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 4-carbamoyl-4-methyl-piperidine-1-carboxylic acid tert-butyl ester (2.1 g, 8.7 mmol) in THF (30 mL) was added Lawesson's reagent (3.5 g, 8.7 mmol) at room temperature. The mixture was heated at 50° C. for 3 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was partitioned between EtOAc and H2O. The organic layer was washed with saturated NaHCO3, and brine. After drying (Na2SO4), the solvent was removed in vacuo, and the residue was purified by silica column chromatography with EtOAc/hexanes to afford the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921350B2
Source datasetuspto-grants-2014_12
ORD IDord-893109f572ae498f98c5583d023ae088
Source noteuspto-grants-2014_12