HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → N-(4-methylsulfonylphenylsulfonyl)-2-chloroisonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-(Methanesulfonyl)benzene-1-sulfonamide | HCID 120313 | — |
| Reactant | 2-Chloropyridine-4-carbonyl chloride | HCID 2800003 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(4-methylsulfonylphenylsulfonyl)-2-chloroisonicotinamide | HCID 13924304 | 74.7% |
Reaction Steps
2.3 g (0.01 mol) of 4-methylsulfonylbenzenesulfonamide were dissolved in 20 ml of pyridine, and added dropwise by 1.7 g (0.01 mol) of 2-chloroisonicotinoyl chloride at room temperature, followed by agitation for 2 hrs. at the same temperature. After acidified by adding aqueous hydrochloric acid, the precipitate was extracted by ethyl acetate. The organic layer obtained was dried and then concentrated to precipitate crude crystals, which were recrystallized by n-hexane/ethyl acetate to 2.8 g (yield: 74.7%) of N-(4-methylsulfonylphenylsulfonyl)-2-chloroisonicotinamide as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04690934 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-e97899d99d384486be14ddeb173e2a60 |
| Source note | uspto-grants-1987_09 |