HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067614Generated: November 2, 2026
Hydrochloric Acid → n-(3,4-Dimethyl-5-isoxazolyl)-5-phenylthiophen-2-sulfonamide
https://huagongshe.com/reaction/1067614
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-(Methoxyethoxymethyl)-N-(3,4-dimethyl-5-isoxazolyl)-5-phenylthiophene-2-sulfonamide | HCID 53733365 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | n-(3,4-Dimethyl-5-isoxazolyl)-5-phenylthiophen-2-sulfonamide | HCID 23445540 | 42% |
Reaction Steps
HCl (3 mL of a 3 N aqueous solution) was added to a solution of N-(methoxyethoxymethyl)-N-(3,4-dimethyl-5-isoxazolyl)-5-phenylthiophene-2-sulfonamide (100 mg, 0.24 mmol) in 3 mL of 95% ethanol and the resulting mixture was refluxed for 6 h. The mixture was then concentrated, diluted with 5 mL of water, neutralized with saturated aqueous sodium bicarbonate solution and acidified to pH 4 using glacial acetic acid. The mixture was extracted with ethyl acetate (2×25 mL) and the combined organic extract was washed with brine (1×5 mL), dried and evaporated. Flash chromatography of the residue on silica gel using 2% MeOH/CHCl3 and further purification by reverse phase HPLC yielded 33.4 mg (42%) of the pure sulfonamide as a white powder, m.p. 176-178° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06248767B1 |
|---|
| Source dataset | uspto-grants-2001_06 |
|---|
| ORD ID | ord-fa37110f40f541bfb3838a3b30616f84 |
|---|
| Source note | uspto-grants-2001_06 |
|---|