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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38044Erstellt: 23. Oktober 2026

4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine → 2-Methylsulfanyl-4-trifluoromethyl-6-[(S)-3-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidin-1-yl]-pyrimidine

https://huagongshe.com/de/reaction/38044

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidineHCID 248063—
EduktPotassium FluorideHCID 522689—
Edukt(S)-3-(2-Trifluoromethyl-benzenesulfonyl)-pyrrolidineHCID 67497015—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-Methylsulfanyl-4-trifluoromethyl-6-[(S)-3-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidin-1-yl]-pyrimidineHCID 86664757—

Reaktionsschritte

(S)-3-(2-Trifluoromethyl-benzenesulfonyl)-pyrrolidine (500 mg) was dissolved in acetonitrile (3.5 mL) in a microwave tube. 4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine (450 mg), TEA (0.75 mL) and KF (10 mg) were added. The reaction mixture was irradiated in the microwave oven at 150° C. for 1.5 h. The reaction mixture was evaporated to dryness and purified by flash chromatography (50 g silica gel, ethyl acetate/n-heptane:0:1→1:0) to yield a light yellow oil (790 mg; 94%) MS: m/z=472.2 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524710B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-426f1c2152a64c8bbebd23636fbb52b5
Quellennotizuspto-grants-2013_09