HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → N-[(6-Bromopyridin-2-yl)sulphonyl]acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Bromopyridine-2-sulfonamide | HCID 57345816 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | N-[(6-Bromopyridin-2-yl)sulphonyl]acetamide | HCID 86667250 | — |
Reaction Steps
6-Bromopyridine-2-sulphonamide (0.5 g, 2.11 mmol, prepared by the methods described in WO2005/058299) and potassium carbonate (2.92 g, 21.1 mmol) were initially charged in acetonitrile (10 ml). While cooling with ice, acetyl chloride (1.16 g, 14.8 mmol) was added dropwise and the reaction mixture was stirred at room temperature for 16 h. The solvent was removed under reduced pressure, and the residue was taken up in water and acidified with dilute hydrochloric acid solution. It was extracted with ethyl acetate and the solvent was removed under reduced pressure. This gave 0.54 g (85% of theory) of N-[(6-bromopyridin-2-yl)sulphonyl]-acetamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08686004B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-e4177b39fa5f40ca9af2143ba7806818 |
| Source note | uspto-grants-2014_04 |