HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bicarbonate → N-benzenesulfonyl-4-acetylamino-3-aminobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide | HCID 18315416 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-benzenesulfonyl-4-acetylamino-3-aminobenzamide | HCID 18680999 | 57.8% |
Reaction Steps
N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide (12.67 g) was dissolved in 200 ml of methanol and 30 ml of water, and 7.59 g of potassium hydrogencarbonate were further added thereto. The mixture was hydrogenated in a hydrogen atmosphere using 2.53 g of 5% palladium on carbon as catalyst at 40° C. for 24 hours. The solid material was separated through filtration, and the filtrate was concentrated. The resulting residue was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and methanol at a ratio of 4:1) to give 6.72 g of N-benzenesulfonyl-4-acetylamino-3-aminobenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166219 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-548c83572ea743bcbf3a231aa47f2ab5 |
| Source note | uspto-grants-2000_12 |