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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 395951Erstellt: 25. Oktober 2026

Chloroform → 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine

https://huagongshe.com/reaction/395951

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktTriethylamineHCID 8471—
Edukt4-Fluorobenzoyl chlorideHCID 67879—
Edukt(2-Aminophenyl)(pyridin-4-yl)methanoneHCID 14005182—
LösungsmittelWaterHCID 962—
Produkt4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridineHCID 18175249—

Reaktionsschritte

4-Fluorobenzoyl chloride (78.0 mg, 0.55 mmol) was added to 4-(2-aminobenzoyl)pyridine (12) (100 mg, 0.50 mmol), triethylamine (0.35 mL, 2.52 mL), and chloroform (5.0 mL) at 23° C. under argon. After 24 h at 23° C., the reaction was poured into water (50 mL), extracted with ethyl acetate (3×50 mL), and dried (MgSO4). After concentration in vacuo, the residue was purified by flash chromatography (ethyl acetate:methylene chloride 1:1) to afford 4-(2-(4-fluoro-N-benzoylamino)benzoyl)pyridine (14): Mass Spectrum (CI) 321 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06605634B2
Quelldatensatzuspto-grants-2003_08
ORD IDord-63470f7b151e47ca901cfe17538a4025
Quellennotizuspto-grants-2003_08