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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1392948Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1392948

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethanolHCID 887—
EduktHydroxyamine hydrochlorideHCID 443297—
EduktSodium MethoxideHCID 10942334—
Edukt2-[4-(4-Acetyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid methyl esterHCID 69201307—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-[4-(4-Acetyl-benzenesulfonyl)-piperazin-1-yl]-thiazole-5-carboxylic acid hydroxyamideHCID 1139576812%

Reaktionsschritte

To a solution of compound (12h) (125 mg, 0.305 mmol) in 1,4-dioxane (2 mL) were added hydroxylamine hydrochloride (211 mg, 3.05 mmol) and a freshly prepared solution of sodium methoxide in methanol (105 mg, 4.57 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 13 h (15 mg, yield 12.0%). HPLC: 92.26% (Rt=12.51 min).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07345043B2
Quelldatensatzuspto-grants-2008_03
ORD IDord-aa264ed95b5846b1b6d3e88b8a69d796
Quellennotizuspto-grants-2008_03