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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748498Generated: October 25, 2026

Toluene → 5-Fluoro-N-(4-hydroxymethyl-2-methanesulfonylphenyl)-3-methylbenzo[b]thiophene-2-sulfonamide

https://huagongshe.com/reaction/748498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantMethyl 4-(5-fluoro-3-methylbenzo[b]thiophene-2-sulfonylamino)-3-methanesulfonylbenzoateHCID 9825353—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product5-Fluoro-N-(4-hydroxymethyl-2-methanesulfonylphenyl)-3-methylbenzo[b]thiophene-2-sulfonamideHCID 2204144370.7%

Reaction Conditions

Temperature-30 °C

Reaction Steps

Into 120 mL of toluene was dissolved 2.08 g of Compound 17. After cooling to −30° C., 22.5 mL of 1.01 mol/L toluene solution of diisobutylaluminum hydride was added thereto. After 5 hours of stirring at the same temperature, water was added to the reaction solution to terminate the reaction and then the mixture was diluted with ethyl acetate, followed by addition of saturated aqueous potassium sodium tartrate solution and 30 minutes of stirring at room temperature. The mixture was extracted with ethyl acetate and the organic layer was washed with saturated brine and then dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure and the resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/1) to obtain 1.38 g of the title compound as colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399781B2
Source datasetuspto-grants-2008_07
ORD IDord-06b887273d9a42499c40658c35b9c91c
Source noteuspto-grants-2008_07