HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966038Generated: October 30, 2026
Fumaric Acid → (3-fluorophenyl)-(S)-pyrrolidin-3-yl-(4-trifluoromethylphenyl)amine difumarate
https://huagongshe.com/reaction/1966038
Participants
| Role | Name | HCID | Charge |
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| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | ((S)-1-benzylpyrrolidin-3-yl)-(3-fluorophenyl)-(4-trifluoromethylphenyl)amine | HCID 66657156 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (3-fluorophenyl)-(S)-pyrrolidin-3-yl-(4-trifluoromethylphenyl)amine difumarate | HCID 66657271 | 78.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420623B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-404b82c6abbd45729acfd8fb0e1812bb |
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| Source note | uspto-grants-2013_04 |
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