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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363850Generated: October 31, 2026

Diisopropylethylamine → HCID 86686904, compound

https://huagongshe.com/reaction/2363850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Bis(trifluoromethyl)benzenesulphonyl chlorideHCID 520945—
ReactantHCID 86686887HCID 86686887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86686904HCID 8668690442%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691993B2
Source datasetuspto-grants-2014_04
ORD IDord-e982813acce24289b7e3eb9166a6e50c
Source noteuspto-grants-2014_04