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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738306Generated: November 1, 2026

Pyridine → HCID 22125701, compound

https://huagongshe.com/reaction/1738306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BisulfateHCID 516919—
ReactantHCID 22125720HCID 22125720—
SolventDichloromethaneHCID 6344—
ProductHCID 22125701HCID 2212570175%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962531
Source datasetuspto-grants-1999_10
ORD IDord-2e14381163c34fee978759c6bda07f07
Source noteuspto-grants-1999_10