HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 4-[3-(N-benzyl-N-acetylamino)propylthio]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[3-(N-benzylamino)propylthio)pyridine | HCID 19079190 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(N-benzyl-N-acetylamino)propylthio]pyridine | HCID 19079243 | 84.3% |
Reaction Steps
To a solution of 1.0 g (3.87 mmol) of 4-[3-(N-benzylamino)propylthio)-pyridine and 0.65 ml (4.64 mmol) of triethylamine in 25 ml of methylene chloride, 0.49 ml (4.64 mmol) of acetyl chloride was added under ice-cooling with stirring. The mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with a saturated aqueous solution of sodium bicarbonate and water and dried, and then the solvent was distilled off. The residue was purified by column chromatography (eluent: chloroform/methanol=25:1) to obtain 980 mg of the desired compound (yield: 84.2%, yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05389658 |
| Source dataset | uspto-grants-1995_02 |
| ORD ID | ord-c0bc651dd1ab4be19615008527ba3724 |
| Source note | uspto-grants-1995_02 |