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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392941Generated: November 2, 2026

Hydrochloric Acid → 2-[4-(4-Trifluoromethoxy-benzene sulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamide

https://huagongshe.com/reaction/1392941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantSodium MethoxideHCID 10942334—
Reactant2-[4-(4-Trifluoromethoxy-benzene sulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid methyl esterHCID 69199216—
Solvent1,4-DioxaneHCID 31275—
Product2-[4-(4-Trifluoromethoxy-benzene sulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamideHCID 11236322—

Reaction Steps

To a solution of compound (12d) (125 mg, 0.276 mmol) in 1,4-dioxane (2 mL) were added hydroxylamine hydrochloride (191 mg, 2.76 mmol) and a freshly prepared solution of sodium methoxide in methanol (95 mg, 4.14 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 13d as a solid. HPLC: =92% (Rt=14.16 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07345043B2
Source datasetuspto-grants-2008_03
ORD IDord-a0d2ec86bbe94a1a884a3bdcc76c2435
Source noteuspto-grants-2008_03