HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 410602Generated: October 27, 2026
hydroxylamine-O-sulfonic acid → (5-Bromo-1,3-thiazol-2-yl)methanesulfonamide
https://huagongshe.com/reaction/410602
Participants
| Role | Name | HCID | Charge |
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| Reactant | hydroxylamine-O-sulfonic acid | HCID 76284 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | Methyl 3-((5-bromothiazol-2-yl)methylsulfonyl)propanoate | HCID 67257798 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Bromo-1,3-thiazol-2-yl)methanesulfonamide | HCID 67257311 | 48.2% |
Reaction Steps
The product of Step 3 (1.244 g, 3.79 mmol) was taken up in THF (50 mL) at room temperature, and NaOMe (25% in MeOH, 0.819 g, 3.79 mmol) was added. After 30 min at room temperature, the suspension was evaporated to dryness, providing a yellow solid. The solid was taken up in water (25 mL), and a solution of NaOAc (1.710 g, 20.85 mmol) and hydroxylamine-O-sulfonic acid (2.143 g, 18.95 mmol) in water (12.5 mL) was added while cooling the reaction (0° C.). The reaction was vigorously stirred at room temperature overnight. The reaction was extracted with ethyl acetate (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated. Flash chromatography (dry load, 10-100% EtOAc/hexanes) afforded 1-(5-bromo-1,3-thiazol-2-yl)methanesulfonamide (470 mg, 48%) as a colorless solid. MS ESI: [M+H]+ m/z 256.9/258.9.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759366B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f0666ffe5aab4687af190c8c49c4b18a |
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| Source note | uspto-grants-2014_06 |
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