Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2211689Generated: November 1, 2026

N,N,N',N'-Tetramethylethylenediamine → [3,5-difluoro-4-(tetrahydro-4-hydroxy-2H-thiopyran-4-yl)phenyl]carbamic Acid, 1-methylethyl Ester

https://huagongshe.com/reaction/2211689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N,N',N'-TetramethylethylenediamineHCID 8037—
ReactantTetrahydrothiopyran-4-oneHCID 66173—
ReactantIsopropyl 3,5-difluoro-phenylcarbamateHCID 58978077—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product[3,5-difluoro-4-(tetrahydro-4-hydroxy-2H-thiopyran-4-yl)phenyl]carbamic Acid, 1-methylethyl EsterHCID 86598977—

Reaction Steps

n-Butyllithium (2.5M in hexanes, 57.2 mL, 0.143 mol) was added dropwise with stirring at −78° C. to (3,5-difluoro-phenyl)-carbamic acid isopropyl ester (15.0 g, 0.07 mol) and N,N,N′,N′-tetramethylethylenediamine (21.04 mL, 0.139 mol) in THF (150 mL), and stirred for 20 min at this temperature. Tetrahydrothiopyran-4-one (8.50 g, 0.073 mol) dissolved in THF (10 mL) was then added dropwise at −78° C., stirred for 1 h, and then allowed to warm to room temperature. The reaction was stirred for another hour and then quenched with saturated aqueous ammonium chloride (100 mL). The reaction mixture was extracted with ethyl acetate, the extracts washed with brine, dried (MgSO4), and evaporated. The residue was purified by flash column chromatography (30% ethyl acetate/hexane) to give the title compound as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101874B2
Source datasetuspto-grants-2006_09
ORD IDord-118f42b147454f878e37e6dc9239ee19
Source noteuspto-grants-2006_09