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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 237586Erstellt: 24. Oktober 2026

Sodium Carbonate → 6-(4-Amino-3,5-dimethylphenyl)-3-methylpyrimidin-4(3H)-one

https://huagongshe.com/de/reaction/237586

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt6-Chloro-3-methylpyrimidin-4(3H)-oneHCID 4366471—
Edukt2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 56737724—
LösungsmittelDimethylformamideHCID 6228—
Produkt6-(4-Amino-3,5-dimethylphenyl)-3-methylpyrimidin-4(3H)-oneHCID 86697249—

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

In a microwave vial 2,6-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (5.6 g) and 6-chloro-3-methylpyrimidin-4(3H)-one (3 g) are suspended in N,N-dimethylformamide (30 mL) and Na2CO3 (26 mL of a 2M aqueous solution). The mixture is purged for 5 minutes with argon. [1,1′-Bis(diphenylphosphino)-ferrocene]-dichloropalladium dichloromethane complex (508 mg) is added, the vial is sealed and the mixture is stirred at 65° C. for 12 hours. After cooling to room temperature the mixture is Partitioned between water and ethyl acetate. The aqueous phase is extracted twice with ethyl acetate and the combined organic phases are washed with brine and dried (MgSO4). The solvents are evaporated to give the title compound. Yield: 2.6 g; LC (method 11): tR=0.71 min; Mass spectrum (ESI+): m/z=230 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08642585B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-c31715c430bd41598881d2f21c3a7fac
Quellennotizuspto-grants-2014_02