HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Bromomethyl)-2,4-difluorobenzene → N-benzenesulfonyl-4-acetylamino-3-(2,4-difluorobenzylamino)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Bromomethyl)-2,4-difluorobenzene | HCID 90297 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | N-benzenesulfonyl-4-acetylamino-3-aminobenzamide | HCID 18680999 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-benzenesulfonyl-4-acetylamino-3-(2,4-difluorobenzylamino)benzamide | HCID 18680987 | — |
Reaction Steps
A solution of 7 ml of methanol containing 0.60 g of N-benzenesulfonyl-4-acetylamino-3-aminobenzamide, 0.656 g of 2,4-difluorobenzyl bromide and 0.423 g of potassium hydrogencarbonate was stirred at 60° C. for 1 hour. The reaction solution was concentrated, and the residue was purified through silica-gel column chromatography (eluent: a mixture of ethyl acetate and methanol at a ratio of 9:1) to give 0.370 g of N-benzenesulfonyl-4-acetylamino-3-(2,4-difluorobenzylamino)benzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166219 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-7bfc105af9fb47028dfd077124cab374 |
| Source note | uspto-grants-2000_12 |