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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(Trifluoromethoxy)benzene-1-sulfonyl chloride | HCID 2777218 | — |
| Reactant | (S)-1-Benzyl-3-(3-amino-phenyl)-pyrrolidine | HCID 68954497 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-((S)-1-Benzyl-pyrrolidin-3-yl)-phenyl]-3-trifluoromethoxy-benzene sulfonamide | HCID 68950079 | 71.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642642B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-d23f90b2704c47e69b34472c8ab892f1 |
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| Source note | uspto-grants-2014_02 |
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