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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262601Generated: October 27, 2026

Stannane, tributyl(1-methylethenyl)- → 2-Fluoro-4-isopropenyl-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/2262601

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannane, tributyl(1-methylethenyl)-HCID 10871254—
ReactantHCID 57470069HCID 57470069—
SolventTetrahydrofuranHCID 8028—
Product2-Fluoro-4-isopropenyl-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamideHCID 5362863697.2%

Reaction Conditions

Temperature150 °C

Reaction Steps

0.2 g of 2-fluoro-4-bromo-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide (0.45 mmol), 1.05 g of tributyl-isopropenyl-stannane (3.17 mmol) and 0.026 g of tetrakistriphenylphosphinpalladium(0) (0.02 mmol) were dissolved in 3 ml of tetrahydrofuran and stirred for 40 minutes at 150° C. in the microwave (CEM). The reaction mixture was filtered over celite, washed with methanol, and the filtrate evaporated to dryness under reduced pressure. The residue was purified via silica gel chromatography with cyclohexane/ethyl acetate (20%), ethyl acetate, and ethyl acetate/methanol (15%). Fractions containing the product were combined, the solvent evaporated to yield 0.176 g of the title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07851463B2
Source datasetuspto-grants-2010_12
ORD IDord-2d9ce1d8e5b64438bafc8bc0841b9227
Source noteuspto-grants-2010_12