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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38797Erstellt: 24. Oktober 2026

Dimethylformamide → 4-{[2-(2,4-Dichlorophenoxy)-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine

https://huagongshe.com/de/reaction/38797

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt2,4-DichlorophenolHCID 8449—
EduktCesium carbonateHCID 10796—
Edukt4-{[2-Chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholineHCID 58168707—
LösungsmittelEthyl AcetateHCID 8857—
Produkt4-{[2-(2,4-Dichlorophenoxy)-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholineHCID 5816891714,8%

Reaktionsschritte

A mixture of 4-{[2-chloro-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine (170 mg), 2,4-dichlorophenol (112 mg), cesium carbonate (225 mg), and N,N-dimethyl formamide (2 mL) was stirred at room temperature for 15 hours, and then at 100° C. for 10 hours. To the reaction liquid was added ethyl acetate (30 mL), followed by washing with saturated brine (20 mL) and a saturated aqueous ammonium chloride solution (20 mL) in this order, the organic layer was dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: chloroform-ethyl acetate) to obtain 4-{[2-(2,4-dichlorophenoxy)-4-(trifluoromethyl)pyrimidin-5-yl]carbonyl}morpholine (36 mg) as a brown oily substance.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524727B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ede3ef95ab5b46a7921b21cd3ced2f4f
Quellennotizuspto-grants-2013_09