Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 216151Erstellt: 24. Oktober 2026

Isopropanol → 4-Chloro-6-(3,4-dimethoxyphenyl)-2-(methylthio)pyrimidine

https://huagongshe.com/de/reaction/216151

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsopropanolHCID 3776—
EduktCesium carbonateHCID 10796—
Edukt4,6-Dichloro-2-(methylthio)pyrimidineHCID 80531—
Edukt3,4-Dimethoxyphenylboronic acidHCID 2734702—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelWaterHCID 962—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt4-Chloro-6-(3,4-dimethoxyphenyl)-2-(methylthio)pyrimidineHCID 5763614683,6%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

Argon is bubbled through a mixture of 4,6-dichloro-2-(methylthio)pyrimidine [4.98 g, 25.55 mmol, Intermediate (29)], 3,4-dimethoxyphenylboronic acid [3.874 g, 21.29 mmol, Intermediate (32)], and Cs2CO3 (17.34 g, 53.23 mmol) in ethylene glycol dimethyl ether (56 mL) and water (14 mL), for a period of 15 minutes. To this mixture is added tetrakis(triphenylphosphine)palladium (0) (1.22 g, 1.06 mmol) the reaction vessel is heated to 100° C. After stirring overnight the mixture is diluted with water (250 mL) and extracted three times with EtOAc (100 mL). The organic extracts are combined, washed with brine (100 mL), and dried over magnesium sulfate. The mixture is filtered and concentrated to provide a solid that is dissolved in boiling isopropyl alcohol (40 mL) and allowed to cool to ambient temperature. After standing for 24 hours the solid is collected by filtration, washed with cold isopropyl alcohol and dried under high vacuum to afford 4-chloro-6-(3,4-dimethoxy-phenyl)-2-methylsulfanyl-pyrimidine [5.28 g, 83.5%, Intermediate (48)].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08193183B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-ebeec63bcd6a4bdfb9ce05b0a1a3d940
Quellennotizuspto-grants-2012_06