HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29041Generated: October 30, 2026
Acetic Anhydride → HCID 9907591, compound
https://huagongshe.com/reaction/29041
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-[5-Methyl-3-(3-fluorophenyl)isoxazol-4-yl]benzenesulfonamide | HCID 22643585 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 9907591 | HCID 9907591 | 81% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07420061B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-7a074d9672334ea2a0613f6c25f69968 |
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| Source note | uspto-grants-2008_09 |
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