HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363850Generated: October 31, 2026
Diisopropylethylamine → HCID 86686904, compound
https://huagongshe.com/reaction/2363850
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Bis(trifluoromethyl)benzenesulphonyl chloride | HCID 520945 | — |
| Reactant | HCID 86686887 | HCID 86686887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86686904 | HCID 86686904 | 42% |
Reaction Steps
Diisopropylethylamine (0.6 mL, 3.4 mmol) was added at 0° C. to a solution of (6-fluoro-4-piperidin-4-yl-naphthalen-2-yl)-acetic acid methyl ester trifluoroacetate salt (which may be prepared as described above; 150 mg, 0.36 mmol) in tetrahydrofuran (5 mL), and the mixture was stirred at room temperature for 30 min. 3,5-Bis(trifluoromethyl)benzenesulfonyl chloride (available from Sigma-Aldrich; 169 mg, 0.54 mmol) was added and the mixture was stirred at room temperature for 16 h. The solvent was evaporated under reduced pressure. Ethyl acetate was added and the mixture was washed with aqueous NaHCO3 (5 mL) and water (5 mL). The organic layer was dried over Na2SO4, filtered, and evaporated under reduced pressure. The residue was purified by chromatography on silica gel using a Biotage purification system, eluting with 10% ethyl acetate/hexanes, to give {4-[1-(3,5-bis-trifluoromethyl-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (87 mg, 42%) as an off-white solid. MS cald. for C26H23F7NO4S [(M+H)+]: 578, obsd. 578.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691993B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e982813acce24289b7e3eb9166a6e50c |
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| Source note | uspto-grants-2014_04 |
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