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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775364Generated: November 3, 2026

Lawesson's reagent → (E)-4,4,4-Trifluoro-1-[4-(4-methyl-2-pyridyl)piperazin-1-yl]but-2-ene-1-thione

https://huagongshe.com/reaction/1775364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant(E)-4,4,4-Trifluoro-1-[4-(4-methyl-2-pyridyl)piperazin-1-yl]but-2-en-1-oneHCID 71765249—
SolventTetrahydrofuranHCID 8028—
Product(E)-4,4,4-Trifluoro-1-[4-(4-methyl-2-pyridyl)piperazin-1-yl]but-2-ene-1-thioneHCID 8983300520%

Reaction Conditions

Temperature110 °C

Reaction Steps

The residue of step A was dissolved in anhydrous THF (2 ml), Lawesson's reagent (40 mg, 0.2 mmol) was added and the mixture was stirred at 110° C. in closed vial under microwave heating. The mixture was concentrated under reduced pressure and the residue was purified by preparative HPLC (Waters X-Bridge, gradient of water containing 0.1% NH3 and acetonitrile) to yield 12 mg of a solid (0.039 mmol, yield 20% for two steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-9cc89d3558264b7e9878887f2fbe6f7c
Source noteuspto-grants-2016_02