HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → 4-Acetyl-N-(2-pyridyl)benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 4-Acetylbenzenesulfonyl chloride | HCID 266418 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-Acetyl-N-(2-pyridyl)benzenesulfonamide | HCID 22750327 | — |
Reaction Steps
A solution of 13.4 g. of 2-aminopyridine in 300 ml. of pyridine is treated with 31.0 g. of 4-acetylbenzenesulfonyl chloride and the solution is stirred at room temperature for 6 hours. The solution is poured into 1 l. of cold water and the resulting precipitate of 4-acetyl-N-(2-pyridyl)benzenesulfonamide is collected by filtration, washed with water and dried; m.p. 201°-202° C. after crystallization from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04137408 |
| Source dataset | uspto-grants-1979_01 |
| ORD ID | ord-b5d6bb42330e44d7854d8ddd56cd1ea4 |
| Source note | uspto-grants-1979_01 |