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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 549178Erstellt: 26. Oktober 2026

Chlorosuccinimide → 4-fluoro-N-hydroxybenzenecarboximidoyl chloride

https://huagongshe.com/reaction/549178

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChlorosuccinimideHCID 31398—
EduktN-[(4-fluorophenyl)methylidene]hydroxylamineHCID 68017—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-fluoro-N-hydroxybenzenecarboximidoyl chlorideHCID 2756316—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A solution of 4-fluorobenzaldehyde oxime (222 mg, 1.60 mmol) dissolved in 3 mL of DMF was treated with N-chlorosuccinimide (212 mg, 1.60 mmol) and the reaction mixture was heated at 50° C. for 3 hours. The reaction mixture was diluted with 25 mL of ethyl acetate and then washed with H2O (4×20 mL). The organic portion was washed with brine, dried over Na2SO4, filtered and concentrated to give 4-fluoro-N-hydroxybenzenecarboximidoyl chloride as a white solid. The material was dissolved in 10 mL of CH2Cl2 and the solution was cooled to 0° C. A solution of (11S)-11-ethynyl-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinoline (190 mg, 0.76 mmol) dissolved in 3 mL of CH2Cl2 was then added followed by triethylamine (318 μL, 2.29 mmol). The reaction was allowed to warm to ambient temperature overnight. The reaction mixture was concentrated and chromatography (0-2% methanol/CHCl3) gave (11R)-11-[3-(4-fluorophenyl)isoxazol-5-yl]-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinoline as a light-brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07943609B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-2ec4cc00625d460ba25e148e888cf434
Quellennotizuspto-grants-2011_05