HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 22125701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | HCID 22125720 | HCID 22125720 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22125701 | HCID 22125701 | 75% |
Reaction Steps
Pyridine (4.25 ml, 52.1 mmol) and trifluoromethanesulfonic anhydride (4.4 ml, 26.1 mmol) were added to a solution of 5-(4-fluorobenzoyl)-6-hydroxy-2-naphthalenesulfonamide (3.0 g, 8.7 mmol), [prepared as described in step 1 above], in methylene chloride (50 ml) at 0° C. After 0.5 h, 1N sodium bisulfate was added and the stirring was continued for an additional 30 minutes. The organic layer was separated, washed with brine, and dried over sodium sulfate. The solvent was removed in vacuo to give 3.1 g of 5-(4-fluorobenzoyl)-6-trifluoromethylsulfonyloxy-2-naphthalenesulfonamide as an oil (75% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06150397 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-0023a2fc88fb41a0a23406a1f1c6134e |
| Source note | uspto-grants-2000_11 |