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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392944Generated: October 27, 2026

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

https://huagongshe.com/reaction/1392944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
Reactant2-[4-(4-Trifluoromethyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid methyl esterHCID 69201003—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-(4-Trifluoromethyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamideHCID 1148739216%

Reaction Steps

To a solution of compound 12f (125 mg, 0.287 mmol) in 1,4-dioxane (2 mL) were added hydroxylamine hydrochloride (199 mg, 2.87 mmol) and a freshly prepared solution of sodium methoxide in methanol (99 mg, 4.30 mmol of sodium dissolved in 1 mL of methanol) under a N2 atmosphere. The reaction mixture was stirred at room temperature for 2 h. The reaction mixture was acidified to pH˜6 with 1M HCl and the formed precipitates were filtered off. The filtrate was diluted with ethyl acetate (5 mL) and water (2 mL) and the organic layer was separated. The aqueous layer was washed with ethyl acetate (5 mL) and the combined organic layers were dried on sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by preparative HPLC to give 13f (20 mg, yield 16%). HPLC 85.42% (Rt=14.11 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345043B2
Source datasetuspto-grants-2008_03
ORD IDord-0923a78cb4a84819bcb4b5b38f5b2f5f
Source noteuspto-grants-2008_03