HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → 2-Chloro-5-benzoylaminopyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Chloro-5-benzoylaminopyridine | HCID 9794648 | 105.7% |
Reaction Steps
14.25 g (0.1 mol) of 2-chloro-5-aminomethylpyridine and 11.1 g (0.11 mol) of triethylamine are dissolved in 150 ml of methylene chloride. 14.8 g (0.105 mol) of benzoyl chloride are then added dropwise at about 20° C. and the reaction mixture is subsequently stirred overnight at room temperature. It is washed three times with water and the organic phase is dried and concentrated. 24.6 g (99.8% of theory) of 2-chloro-5-benzoylaminopyridine are obtained as white crystals of melting point 118°-120° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05623076 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-f2161ce8085e4e71a9a2e8a6ca6c75aa |
| Source note | uspto-grants-1997_04 |