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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 450117Erstellt: 25. Oktober 2026

Dimethylformamide → N-(2-Fluoro-4-methylsulfanyl-phenyl)-malonamic acid methyl ester

https://huagongshe.com/reaction/450117

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
EduktTriethylamineHCID 8471—
EduktMethylmalonylchlorideHCID 10931669—
Edukt2-Fluoro-4-(methylsulfanyl)anilineHCID 22025617—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
ProduktN-(2-Fluoro-4-methylsulfanyl-phenyl)-malonamic acid methyl esterHCID 6723458972%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

To a solution of 2-fluoro-4-methylsulfanylphenylamine (13 g, 82.7 mmol), triethylamine (9.3 mL, 86.8 mmol) and DMAP (100 mg, 0.8 mmol) in DMF (50 mL) was added methyl malonyl chloride (11.5 mL, 82.7 mmol). The reaction was heated at 60° C. for 2 hours then concentrated in vacuo. The resultant residue was dissolved in ethyl acetate (30 mL), washed with water (20 mL) and the aqueous fraction extracted twice with ethyl acetate (2×10 mL). The combined organic fractions were washed with brine, dried (MgSO4) and concentrated in vacuo. The resultant residue was subjected to flash chromatography (SiO2, gradient 10-30% ethylacetate in cyclohexane) to yield the title compound as a white solid (15.4 g, 72%). LCMS (Method B): RT=2.94 min, M+H+=258.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08486963B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-f1140ba2357f4cc68ce82a53e0a0b701
Quellennotizuspto-grants-2013_07