Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040082Generated: October 25, 2026

hydroxylamine-O-sulfonic acid → 2-(5-Bromothiazol-2-yl)propane-2-sulfonamide

https://huagongshe.com/reaction/1040082

Reaction equation

Participants

RoleNameHCIDCharge
Reactanthydroxylamine-O-sulfonic acidHCID 76284—
ReactantSodium AcetateHCID 517045—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-{[2-(5-bromo-1,3-thiazol-2-yl)propan-2-yl]sulfonyl}propanoateHCID 67258095—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-(5-Bromothiazol-2-yl)propane-2-sulfonamideHCID 6725703479%

Reaction Steps

The product of Step 4 (2.50 g, 7.02 mmol) was taken up in THF (80 mL) at room temperature, and NaOMe (25% in MeOH, 1.52 g, 7.02 mmol) was added. After 30 min at room temperature, the suspension was evaporated to dryness, providing a white solid. The solid was taken up in water (50 mL), and a solution of NaOAc (3.17 g, 38.6 mmol) and hydroxylamine-O-sulfonic acid (3.97 g, 35.1 mmol) in water (25 mL) was added while cooling the reaction (0° C.). The reaction was vigorously stirred at room temperature overnight (a white solid precipitated after 15-30 min). The reaction was extracted with ethyl acetate (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered and evaporated. The resulting white residue was triturated with CH2Cl2 and filtered to provide 2-(5-bromo-1,3-thiazol-2-yl)propane-2-sulfonamide (1.58 g, 79%) as a white powder. ESI: [M+H]+ m/z 284.9/286.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08551984B2
Source datasetuspto-grants-2013_10
ORD IDord-1a6d3a74a6ac4af1871863178ba790f3
Source noteuspto-grants-2013_10