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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 32646Erstellt: 25. Oktober 2026

Triethylamine → 1-{3-Fluoro-4-[4-(2-fluoro-5-nitrobenzoyl)piperazino]phenyl}-1-ethanone

https://huagongshe.com/reaction/32646

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-(3-Fluoro-4-piperazin-1-ylphenyl)ethanoneHCID 685610—
Edukt2-Fluoro-5-nitrobenzoyl chlorideHCID 10976570—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt1-{3-Fluoro-4-[4-(2-fluoro-5-nitrobenzoyl)piperazino]phenyl}-1-ethanoneHCID 136226768%

Reaktionsschritte

A solution of 2-Fluoro-5-nitro-benzoyl chloride (CAS: 7304-32-7; Feng, Y.; Burgess, K.; Chem.Europ.J.; EN; 5; 11; 1999; 3261-3272) (0.054 g, 0.261 mmol) in dioxane (1 ml) was treated with triethylamine (0.073 ml, 0.522 mmol) and then with a solution of 1-(3-Fluoro-4-piperazin-1-yl-phenyl)-ethanone (CAS: 189763-57-3; WO9714690) (58 mg, 0.261 mmol) in dioxane (1 ml). The mixture was stirred at room temperature for 30 minutes. The solvent was removed in vacuo. The crude oil was taken in water. The aqueous layer was extracted 3 times with CH2Cl2. The combined extracts were dried over Na2SO4, filtered and the solvent was removed in vacuo. The crude gum was purified on silicagel (eluent: heptane/ethylacetate 0%-20% (10 minutes) to provide the title compound (69 mg, 68%) as a light yellow solid, MS (m/e): 390.2 (MH+, 100%)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07427612B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-1895dfa81431463490583c1a94a66577
Quellennotizuspto-grants-2008_09