HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonamide → N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonamide | HCID 7370 | — |
| Reactant | 4-Acetamido-3-nitrobenzoic acid | HCID 73758 | — |
| Reactant | 3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-ene | HCID 53630274 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide | HCID 18315416 | 78.2% |
Reaction Steps
N,N'-carbonyldiimidazole (14.45 g) was added to a solution of 10.00 g of 4-acetylamino-3-nitrobenzoic acid in 300 ml of N,N-dimethylformamide, and the mixture was stirred at room temperature for 1 hour. Subsequently, 14.03 g of benzenesulfonamide and 13.58 g of diazabicycloundecene were added thereto, and the mixture was stirred at 100° C. for 72 hours. The reaction mixture was separated with the addition of chloroform and water. The organic layer was then concentrated, and 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 12.67 g of N-benzenesulfonyl-4-acetylamino-3-nitrobenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166219 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-ad51ec969bcd42e5aee59aaf2d89d0fc |
| Source note | uspto-grants-2000_12 |