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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363842Generated: November 1, 2026

Diisopropylethylamine → HCID 86686900, compound

https://huagongshe.com/reaction/2363842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(Methylsulfonyl)benzenesulfonyl chlorideHCID 220330—
ReactantHCID 86686887HCID 86686887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86686900HCID 8668690064.2%

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. 3-Methylsulfonylbenzenesulfonyl chloride (available from Matrix Scientific; 138 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 20% ethyl acetate/hexanes, to give {6-fluoro-4-[1-(3-methanesulfonyl-benzenesulfonyl)-piperidin-4-yl]-naphthalen-2-yl}-acetic acid methyl ester (120 mg, 64%) as an off-white solid. MS cald. for C25H27FNO6S2 [(M+H)+]: 520, obsd. 520.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691993B2
Source datasetuspto-grants-2014_04
ORD IDord-af5ce1e105e34ae095eaf36a63de2fa3
Source noteuspto-grants-2014_04