HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → N-(2-Benzoylphenyl)-4-(2-oxopyrrolidin-1-yl)benzene-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-Bromobutyric acid | HCID 75809 | — |
| Reactant | 4-Amino-N-(2-benzoylphenyl)benzene-1-sulfonamide | HCID 69308994 | — |
| Solvent | HCID 20373099 | HCID 20373099 | — |
| Product | N-(2-Benzoylphenyl)-4-(2-oxopyrrolidin-1-yl)benzene-1-sulfonamide | HCID 58664932 | — |
Reaction Steps
A solution of 474 mg (2.84 mmol) of 4-bromo-butanoic acid in 6 mL of 5:1 HMPA/acetonitrile was cooled to 0 deg and thionyl chloride (0.207 mL, 2.84 mmol) was added. The reaction mixture was warmed to room temperature, and transferred to a flask containing 250 mg (0.709 mmol) of neat 4-amino-N-(2-benzoylphenyl)benzenesulfonamide. The solution was allowed to stir overnight. The reaction was quenched w/saturated sodium bicarbonate and diluted with EtOAc (˜100 mL), washed with water (3×20 mL) and brine (1×20 mL), dried over sodium sulfate, filtered, and concentrated in vacuo. The residue was purified via flash chromatography (15% to 75% EtOAc/hexanes)to provide the title compound. LC/MS (ES MS, M+H+ found: 457).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07393873B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-a77776605ad14b689a350caad336b178 |
| Source note | uspto-grants-2008_07 |