Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 394026Generated: October 30, 2026

Allyl bromide → HCID 69101508, compound

https://huagongshe.com/reaction/394026

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 10984804HCID 10984804—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductHCID 69101508HCID 69101508—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 37 mg of (2R)-N-((3S)-3-piperidylmethyl)-1-{(2S)-1-(3,3,3-triphenylpropanoyl)pyrrolidin-2-yl}carbonylpyrrolidine-2-carboxamide in 0.9 ml of acetonitrile, 0.0055 ml of allyl bromide and 25 mg of potassium carbonate were added at room temperature, followed by 1.5 hours' stirring at 80° C. under heating. The reaction liquid was diluted with chloroform, washed successively with water and 1N aqueous sodium hydroxide solution, and dried over anhydrous sodium sulfate. After distilling the solvent off under reduced pressure, the resulting residue was purified with a preparative thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (Merck), chloroform/methanol/28% aqueous ammonia=100/10/1), to provide 23 mg of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06809108B1
Source datasetuspto-grants-2004_10
ORD IDord-cbf4d3c95cf64820a6faa57d34450b31
Source noteuspto-grants-2004_10