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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392955Generated: November 3, 2026

Hydrochloric Acid → 2-[4-(4-Fluoro-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamide

https://huagongshe.com/reaction/1392955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 69197132HCID 69197132—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-(4-Fluoro-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamideHCID 11485984—

Reaction Steps

To a solution of compound (12m) (125 mg, 0.320 mmol) in 1,4-dioxane (2 mL) were added hydroxylamine hydrochloride (225 mg, 3.20 mmol) and a freshly prepared solution of sodium methoxide in methanol (110 mg, 4.80 mmol of sodium dissolved in 1 mL of methanol) under a N2 atmosphere. The reaction mixture was stirred at room temperature for 2 h (progress of the reaction was monitored by TLC analysis). The reaction mixture was acidified to pH˜6 with 1M HCl and the formed precipitates were filtered off. The filtrate was diluted with ethylacetate (5 mL) and water (2 mL) and the organic layer was separated. The aqueous layer was washed with ethylacetate (5 mL) and the combined organic layers were dried on sodium sulphate, filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC to give 13m. HPLC: (Rt=3.89 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345043B2
Source datasetuspto-grants-2008_03
ORD IDord-3962bca049b7498795da7bd5dab91e1e
Source noteuspto-grants-2008_03