HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871901Generated: October 30, 2026
Lawesson's reagent → HCID 57473378, compound
https://huagongshe.com/reaction/871901
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | tert-Butyl 4-carbamoyl-4-methylpiperidine-1-carboxylate | HCID 53393793 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57473378 | HCID 57473378 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975258B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-ae0ba642a29740f99b43d13b9b78b6d2 |
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| Source note | uspto-grants-2015_03 |
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