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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584230Generated: November 2, 2026

Acetic Anhydride → HCID 9907591, compound

https://huagongshe.com/reaction/1584230

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant4-[5-Methyl-3-(3-fluorophenyl)isoxazol-4-yl]benzenesulfonamideHCID 22643585—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9907591HCID 990759181%

Reaction Steps

Acetic anhydride (1.01 g, 9.39 mmol) and triethylamine (0.401 g, 3.97 mmol) were added to a solution of 4-[5-methyl-3-(3-fluorophenyl)isoxazol-4-yl]benzenesulfonamide (1.10 g, 3.31 mmol) and N,N-dimethylpyridine (0.202 g) in dry tetrahydrofuran. After stirring for 18 hours at room temperature, the reaction mixture was concentrated. The residue was dissolved in ethyl acetate, washed successively with 1N hydrochloric acid and brine, dried over anhydrous MgSO4 and concentrated to afford 1.0 g (81%) of the desired product as a crystalline product: mp 144-145° C. 1H NMR (CDCl3) 8.00 (d, 2H, J=7.3 Hz), 7.30-7.27 (m, 4H), 7.10-7.06 (m, 3H), 2.46 (s, 3H), 1.99 (s, 3H). Anal. Calc'd for C18H15FN2O4S: C, 57.75; H, 4.04; N, 7.48. Found: C, 57.84; H, 4.06; N, 7.49.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932598
Source datasetuspto-grants-1999_08
ORD IDord-a9bd592a06e6423cbd76c33d27c59740
Source noteuspto-grants-1999_08