HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[3-(4-Chlorobenzoylamino)propylthio]pyridine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | 4-(3-Aminopropylthio)pyridine dihydrochloride | HCID 19079259 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[3-(4-Chlorobenzoylamino)propylthio]pyridine hydrochloride | HCID 19079195 | 118.6% |
Reaction Steps
To a solution of 1.00 g (4.15 mmol) of 4-(3-aminopropylthio)pyridine dihydrochloride and 2.77 ml (19.8 mmol) of triethylamine in 40 ml of methylene chloride was added 0.63 ml (4.96 mmol) of 4-chlorobenzoyl chloride under ice-cooling with stirring and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was washed with an aqueous saturated sodium bicarbonate solution and water and dried. The solvent was distilled off. The residue was purified by column chromatography (eluent: ethyl acetate) to obtain the powder which was washed with ether and dried to obtain 1.01 g of the desired compound (free base) (79.3%, pale yellow powder), mp: 95.0°-96.0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05457106 |
| Source dataset | uspto-grants-1995_10 |
| ORD ID | ord-bd236310fc0d47d09718391e1e869f74 |
| Source note | uspto-grants-1995_10 |