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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426697Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 67397692, compound

https://huagongshe.com/reaction/1426697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant15-Crown-5HCID 36336—
ReactantHCID 67396635HCID 67396635—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67397692HCID 6739769272%

Reaction Steps

To a solution of 1-(2,4-dimethoxyphenyl)-N-{[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}-N-methylmethanamine (2.98 g) in tetrahydrofuran (20 mL) was added sodium hydride (60% in oil, 421 mg) under ice-cooling. After stirring at the same temperature for 30 min, 15-crown-5 (1.80 mL) was added dropwise. After further stirring for 15 min, benzenesulfonyl chloride (1.15 mL) was added dropwise. After stirring for 1 hr at the same temperature, saturated aqueous ammonium chloride solution and water were added, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (eluent: hexane:ethyl acetate=9:1→7:3) to give the title compound as a yellow oil (yield 2.95 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933105B2
Source datasetuspto-grants-2015_01
ORD IDord-de6a5086359746faa6a90d8ee5c41f42
Source noteuspto-grants-2015_01