HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 4-[3-(N-2-pyridylmethyl-N-benzoylamino)propylthio]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| 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-benzoylamino)propylthio]pyridine | HCID 19079150 | 58.9% |
Reaction Steps
To a solution of 1.60 g (6.17 mmol) of 4-[3-(N-2-pyridylmethylamino)propylthio)pyridine and 1.05 ml (7.40 mmol) of triethylamine in 10 ml of methylene chloride, 0.86 ml (7.40 mmol) of benzoyl 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: ethyl acetate/methanol=10:1) to obtain 1.32 g of the desired compound (yield: 58.9%, yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05767121 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-5a2b1dc2266748bca3fb47d0aae9ad96 |
| Source note | uspto-grants-1998_06 |