HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine → 2-Methylsulfanyl-4-trifluoromethyl-6-[(S)-3-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidin-1-yl]-pyrimidine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Chloro-2-(methylsulfanyl)-6-(trifluoromethyl)pyrimidine | HCID 248063 | — |
| Edukt | Potassium Fluoride | HCID 522689 | — |
| Edukt | (S)-3-(2-Trifluoromethyl-benzenesulfonyl)-pyrrolidine | HCID 67497015 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 2-Methylsulfanyl-4-trifluoromethyl-6-[(S)-3-(2-trifluoromethyl-benzenesulfonyl)-pyrrolidin-1-yl]-pyrimidine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08524710B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-426f1c2152a64c8bbebd23636fbb52b5 |
| Quellennotiz | uspto-grants-2013_09 |