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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79667Generated: October 26, 2026

Lawesson's reagent → HCID 66620801, compound

https://huagongshe.com/reaction/79667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant2-[2-(4-Bromo-phenyl)-2-oxo-ethylcarbamoyl]-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 58310150—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66620801HCID 6662080165.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

The mixture of 2-[2-(4-Bromo-phenyl)-2-oxo-ethylcarbarnoyl]-pyrrolidine-1-carboxylic acid tert-butyl ester (1.0 g, 2.44 mmol) and Lawesson's reagent (1.23 g, 3.0 mmol) in THF (16 ml) was heated at 80° C. for 4 hours. The solvent was removed under reduced pressure and the mixture was diluted with EtOAc. The organic phase was washed with saturated sodium bicarbonate, water, and brine, and was dried with sodium sulfate. Concentration and purification by flash column chromatography (hexanes/EtOAc) gave 2-[5-(4-Bromo-phenyl)-thiazol-2-yl]-pyrrolidine-1-carboxylic acid tert-butyl ester (655 mg). m/z: 410.7 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841278B2
Source datasetuspto-grants-2014_09
ORD IDord-0a28bee9139a426da148f38494765087
Source noteuspto-grants-2014_09