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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 238970Generated: October 25, 2026

Triethylamine → N-[3-((S)-1-Benzyl-pyrrolidin-3-yl)-phenyl]-3-trifluoromethoxy-benzene sulfonamide

https://huagongshe.com/reaction/238970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-(Trifluoromethoxy)benzene-1-sulfonyl chlorideHCID 2777218—
Reactant(S)-1-Benzyl-3-(3-amino-phenyl)-pyrrolidineHCID 68954497—
SolventTetrahydrofuranHCID 8028—
ProductN-[3-((S)-1-Benzyl-pyrrolidin-3-yl)-phenyl]-3-trifluoromethoxy-benzene sulfonamideHCID 6895007971.6%

Reaction Steps

(S)-1-Benzyl-3-(3-amino-phenyl)-pyrrolidine (0.4 g, 1.59 mmol) and commercially available 3-trifluoromethoxy-benzene sulfonylchloride (0.39 g, 1.5 mmol) were dissolved in 30 ml tetrahydrofurane. 0.66 ml of triethylamine (3.75 mmol) were added and the mixture was stirred for 16 h at room temperature. The solvent was evaporated under reduced pressure and the residue was treated with water/diethylether. After adjusting the aqueous phase to alkaline pH with 1 N aqueous NaOH, the aqueous layer was extracted with diethylether and the combined organic layers dried over magnesium sulfate, filtered and evaporated. The product was purified via silica gel chromatography using an Isco Companion semi-automated chromatography system to yield 0.512 g of the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08642642B2
Source datasetuspto-grants-2014_02
ORD IDord-d23f90b2704c47e69b34472c8ab892f1
Source noteuspto-grants-2014_02