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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1801571Erstellt: 25. Oktober 2026

Diisopropylethylamine → N-(2-chloro-5-formylphenyl)-5-methylisoxazole-3-carboxamide

https://huagongshe.com/reaction/1801571

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3-Amino-4-chlorobenzaldehydeHCID 245303—
Edukt5-Methylisoxazole-3-carbonyl chlorideHCID 2736894—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelEthyl AcetateHCID 8857—
ProduktN-(2-chloro-5-formylphenyl)-5-methylisoxazole-3-carboxamideHCID 5980318225,8%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a solution of 3-amino-4-chlorobenzaldehyde 2 (0.267 g, 1.72 mmol) in DCM (5 mL) at 0° C. was added N-ethyl-N-isopropylpropan-2-amine (0.600 mL, 3.44 mmol) and 5-methylisoxazole-3-carbonyl chloride (0.292 g, 2.01 mmol). The reaction mixture was stirred at 0° C. for 30 min, warmed to room temperature, stirred for 1 h, and diluted with EtOAc. The organic phase was washed with saturated NaHCO3 (1×), brine (1×), dried over MgSO4, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluted with 15% to 50% EtOAc in hexanes) gave N-(2-chloro-5-formylphenyl)-5-methylisoxazole-3-carboxamide 3 (0.117 g, 25.8% yield) as a white solid. Mass spectrum: calculated for C12H9ClN2O3 264.0. found 265.0 (M++1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08349831B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-97b7ab958b164becbed46e3827144cf0
Quellennotizuspto-grants-2013_01