HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → 4-[3-(N-2-pyridylmethyl-N-acetylamino)propylthio]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(3-(N-2-pyridylmethylamino)propylthio]pyridine | HCID 19079176 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(N-2-pyridylmethyl-N-acetylamino)propylthio]pyridine | HCID 19079165 | 85.6% |
Reaction Steps
To a solution of 1.62 g (6.24 mmol) of 4-[3-(N-2-pyridylmethylamino)propylthio]pyridine and 1.10 ml (7.80 mmol) of triethylamine in 10 ml of methylene chloride, 0.51 ml (7.80 mmol) of acetyl chloride was added under ice-cooling with stinting. 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 the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate/methanol=10:1) to obtain 1.61 g of the desired compound (yield: 85.6%, yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561147 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-412a60e9636747be9cdc70e903f7e5e6 |
| Source note | uspto-grants-1996_10 |