HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1746404Generated: October 30, 2026
Potassium Fluoride → N-(2,4-dimethylphenyl)-N-isobutyl-4-(pyridine-4-ylmethoxy)benzenesulfonamide
https://huagongshe.com/reaction/1746404
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | 4-(Bromomethyl)pyridine | HCID 642799 | — |
| Reactant | N-(2,4-dimethylphenyl)-4-hydroxy-N-isobutylbenzenesulfonamide | HCID 71543523 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-(2,4-dimethylphenyl)-N-isobutyl-4-(pyridine-4-ylmethoxy)benzenesulfonamide | HCID 71543524 | — |
Reaction Steps
A mixture of N-(2,4-dimethylphenyl)-4-hydroxy-N-isobutylbenzenesulfonamide (33 mg, 0.099 mmol), and potassium fluoride, 40% by weight on alumina (40% KF.Al2O3 43.1 mg, 0.297 mmol) in acetonitrile (0.2 mL) were stirred for 5 mins, before addition of 4-(bromomethyl)pyridine (0.099 mmol) in acetonitrile (0.2 mL). The reaction mixture was capped and stirred at RT for 18 hours. Additional 40% KF.Al2O3 (43 mg) and more alkylating reagent (0.1 mmol) were added to the tube, which was capped and stirred for a further 18 hours. The reaction had additional potassium fluoride, 40% by weight on alumina (43 mg) and alkylating reagent (0.1 mmol), and then recapped and stirred for 2 days. The sample was filtered through cotton wool, and DMSO added to bring the total volume to 1 mL. The solutions were purified by mass directed autoprep on Sunfire C18 column using acetonitrile water with a formic acid modifier. The solvent was dried under a stream of nitrogen in the Radleys blowdown apparatus to give the required product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09150508B2 |
|---|
| Source dataset | uspto-grants-2015_10 |
|---|
| ORD ID | ord-52d4d1f0e70d4850880fa7f4ab8688c7 |
|---|
| Source note | uspto-grants-2015_10 |
|---|