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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408876Generated: October 30, 2026

Fumaric Acid → (3-fluorophenyl)-(S)-pyrrolidin-3-yl-(4-trifluoromethylphenyl)amine difumarate

https://huagongshe.com/reaction/2408876

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFumaric AcidHCID 444972—
Reactant1-Chloroethyl chloroformateHCID 521305—
Reactant((S)-1-benzylpyrrolidin-3-yl)-(3-fluorophenyl)-(4-trifluoromethylphenyl)amineHCID 66657156—
SolventDichloromethaneHCID 6344—
Product(3-fluorophenyl)-(S)-pyrrolidin-3-yl-(4-trifluoromethylphenyl)amine difumarateHCID 6665727178.4%

Reaction Steps

To a 1,2-dichloromethane solution (1 ml) containing ((S)-1-benzylpyrrolidin-3-yl)-(3-fluorophenyl)-(4-trifluoromethylphenyl)amine (0.48 g, 1.1 mmol) was added 1-chloroethyl chloroformate (0.82 g, 5.8 mmol). The mixture was stirred at room temperature for 15 hours and heated under reflux for 3 hours. The solvent was distilled off under reduced pressure, and 5 ml methanol was then added to the residue and heated under reflux for 3 hours. After distilling the solvent off under reduced pressure, the residue was then dissolved in dichloromethane and washed with an aqueous saturated sodium hydrogencarbonate solution. After drying over magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was dissolved in ethanol, fumaric acid (128 mg, 1.1 mmol) was then added thereto, giving a uniform solution. The solvent was distilled off under reduced pressure, and the crystals produced by adding dichloromethane to the residue were separated by filtration and dried, giving 0.24 g of light brown powdery (3-fluorophenyl)-(S)-pyrrolidin-3-yl-(4-trifluoromethylphenyl)amine difumarate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815871B2
Source datasetuspto-grants-2014_08
ORD IDord-af137c28419748c5a780b65249030a7d
Source noteuspto-grants-2014_08