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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363840Generated: October 30, 2026

4-Chlorobenzenesulfonyl chloride → HCID 86686899, compound

https://huagongshe.com/reaction/2363840

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86686887HCID 86686887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86686899HCID 8668689950.2%

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. 4-Chlorobenzenesulfonyl chloride (available from Sigma-Aldrich; 114 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-(4-chloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (86 mg, 50%) as a white solid. MS cald. for C24H24ClFNO4S [(M+H)+]: 476, obsd. 476.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691993B2
Source datasetuspto-grants-2014_04
ORD IDord-6cbb89db0a8e436ba662a92354d8ff11
Source noteuspto-grants-2014_04