HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 4-[3-(N-(2-thienylmethyl)-N-benzoylamino)propylthio]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(3-(N-(2-thienylmethyl)amino)propylthio]pyridine | HCID 19079184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(N-(2-thienylmethyl)-N-benzoylamino)propylthio]pyridine | HCID 19079117 | 35.9% |
Reaction Steps
To a solution of 2..5 g (9.45 mmol) of 4-[3-(N-(2-thienylmethyl)amino)propylthio]pyridine and 1.32 ml (9.45 mmol) of triethylamine in 50 ml of methylene chloride, 1.1 ml (9.45 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 the solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain 1.25 g of the desired compound (yield: 35.9%, yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05561147 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-00943ad703184e6b89c0f98563d42ece |
| Source note | uspto-grants-1996_10 |