HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-{5-[(tert-Butylamino)sulfonyl]-4-methyl-1,3-thiazol-2-yl)acetamide → N-(4-methyl-5-sulfamoylthiazol-2-yl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-{5-[(tert-Butylamino)sulfonyl]-4-methyl-1,3-thiazol-2-yl)acetamide | HCID 59257550 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | N-(4-methyl-5-sulfamoylthiazol-2-yl)acetamide | HCID 3244062 | — |
Reaction Steps
A solution of N-{5-[(tert-butylamino)sulfonyl]-4-methyl-1,3-thiazol-2-yl}acetamide (1.1 g) in TFA (10 ml) was stirred at room temperature for 3 d. The mixture was evaporated, redissolved in TFA (10 ml) and stirred for a further ld. On evaporation the resulting oil was azeotroped with DCM (×2) and triturated with Et2O to give the subtitle compound as a beige solid. Yield 0.7 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08410123B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-e6386032672848088ba611d5c847ac0c |
| Source note | uspto-grants-2013_04 |