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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516482Generated: November 1, 2026

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

https://huagongshe.com/reaction/1516482

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 numberUS08227495B2
Source datasetuspto-grants-2012_07
ORD IDord-b8e9e93999d24ab3a03132a8217ad1e6
Source noteuspto-grants-2012_07