HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260216Generated: 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/1260216
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannane, tributyl(1-methylethenyl)- | HCID 10871254 | — |
| Reactant | HCID 57470069 | HCID 57470069 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Fluoro-4-isopropenyl-N-[4-((S)-1-propyl-pyrrolidin-3-yl)-phenyl]-benzenesulfonamide | HCID 53628636 | 97.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08470810B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-dad33c5c6478474d9c0cb822931c35b5 |
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| Source note | uspto-grants-2013_06 |
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