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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363848Generated: October 31, 2026

Diisopropylethylamine → HCID 86686903, compound

https://huagongshe.com/reaction/2363848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3,5-Dichlorobenzenesulfonyl chlorideHCID 522388—
ReactantHCID 86686887HCID 86686887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86686903HCID 8668690342.4%

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-Dichlorobenzenesulfonyl chloride (available from Sigma-Aldrich; 133 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-dichloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (78 mg, 42%) as a sticky off-white solid. MS cald. for C24H23Cl2FNO4S [(M+H)+]: 510, obsd. 510.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691993B2
Source datasetuspto-grants-2014_04
ORD IDord-af5ca075c63e45ec81e2cfbd6fa621ac
Source noteuspto-grants-2014_04