HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307403Generated: October 30, 2026
Trifluoroacetic acid → HCID 69748185, compound
https://huagongshe.com/reaction/2307403
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 60128267 | HCID 60128267 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69748185 | HCID 69748185 | — |
Reaction Steps
A solution of t-butyl (2S)-2-[(1H-indazol-4-yloxy)methyl]pyrrolidine-1-carboxylate (0.317 g, 1.0 mmol) in dimethylformamide is treated with sodium hydride (0.08 g, 2.0 mmol, 60% in mineral oil) at room temperature, stirred for 10 min, treated with benzenesulfonyl chloride (0.264 g, 1.5 mmol), stirred for 18 h under nitrogen at room temperature, quenched with water and diluted with ether. The organic phase is separated, washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo to give a white foam residue. The residue is purified by chromatography (silica gel, EtOAc:hexanes, 15:85) to give a white solid. This solid is dissolved in trifluoroacetic acid at 0° C., stirred at room temperature for 90 min and concentrated in vacuo. The resultant residue is triturated under ether to afford the title compound as a white solid, 300 mg, mp 218-219° C., identified by NMR and mass spectral analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831094B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-0fe23fd934124464aeea9c3c14132dab |
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| Source note | uspto-grants-2004_12 |
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