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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1509840Erstellt: 24. Oktober 2026

Niclosamide → 4-Chloro-2-(2-chloro-4-nitrophenylcarbamoyl)phenyl benzoate

https://huagongshe.com/de/reaction/1509840

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNiclosamideHCID 4477—
EduktBenzoyl chlorideHCID 7412—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelPyridineHCID 1049—
Produkt4-Chloro-2-(2-chloro-4-nitrophenylcarbamoyl)phenyl benzoateHCID 23966630—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

A suspension of 5-Chloro-N-(2-chloro-4-nitrophenyl)-2-hydroxybenzamide (1.27 g., 3.88 mmol) in pyridine (15 mL) was treated with 4-dimethylaminopyridine (30 mg) and benzoyl chloride (0.49 mL, 4.27 mmol) was introduced dropwise. The suspension was warmed to 50° C. for one hour then cooled to room temperature and stirred for 17 hours. The reaction mixture was partitioned between 1N aqueous HCl and ethyl acetate. The ethyl acetate phase was washed with water, then brine, dried over magnesium sulfate, and concentrated to an off-white solid. This was recrystallized from ethyl acetate/hexanes. 1HNMR (500 MHz, DMSO-d6): δ7.70 (M, 3H), 7.73 (m, 2H), 7.89 (m, 1H), 7.93 (M, 1H), 8.19 (m, 1H), 8.32 (m, 1H), 10.60 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08211882B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-c46173826d29412897e87d842c4660f2
Quellennotizuspto-grants-2012_07