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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874968Generated: October 30, 2026

Lawesson's reagent → HCID 86673534, compound

https://huagongshe.com/reaction/874968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant4-(t-Butoxycarbonyl)-1-methylpiperazine-2-carboxamideHCID 23145920—
SolventTolueneHCID 1140—
ProductHCID 86673534HCID 8667353479.9%

Reaction Steps

tert-Butyl 3-carbamoyl-4-methylpiperazine-1-carboxylate (400 mg, 1.64 mmol) was dissolved in toluene (20 mL) and Lawesson reagent (332 mg, 0.82 mmol) was added. The reaction mixture was heated to reflux for 5 h. Solvent was removed under reduced pressure and the crude product was purified by column chromatography (silica gel 60-120 mesh, eluent 10-15% MeOH in CHCl3) to afford tert-butyl 3-carbamothioyl-4-methylpiperazine-1-carboxylate (0.17 g, yield 40%) as pale yellow liquid. 1H NMR (300 MHz, CDCl3) δ 8.16 (br s, 1H), 7.47 (br s, 1H), 4.28-4.21 (m, 1H), 4.06-3.99 (m, 1H), 3.62 (m, 1H), 3.18-3.13 (dd, J=10.2 Hz, 4.1 Hz, 1H), 2.89-2.82 (m, 2H), 2.52-2.47 (dd, J=11.5 Hz, 3.4 Hz, 1H), 2.26 (s, 3H), 1.47 (s, 9H). MS (ESI) m/z: Calculated for C11H21N3O2S: 259.14. found: 260.2 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08981084B2
Source datasetuspto-grants-2015_03
ORD IDord-de2617fda6c04b889e670b8c74acd34a
Source noteuspto-grants-2015_03