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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50107Erstellt: 25. Oktober 2026

Toluene → Methyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylate

https://huagongshe.com/reaction/50107

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktN-cyano-N-methylmethanesulphonamideHCID 10219456—
EduktHCID 178500902HCID 178500902—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelWaterHCID 962—
ProduktMethyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylateHCID 992982180,3%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

10.0 g (37.7 mmol) of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate were introduced into 50 ml of toluene, together with 10.17 g (75.4 mmol) of N-cyano-N-methylmethanesulphonamide and the mixture was treated at room temperature with 3.61 g (18.9 mmol) of titanium tetrachloride. The reaction progressed exothermically. The red-orange-coloured suspension was heated to 110° C. and stirred for 4.5 h. It was then cooled to room temperature and treated with 30 ml of water. The organic phase was separated off and the aqueous phase was extracted with ethyl acetate (30 ml). The combined organic phases were washed with 30 ml of water and dried over magnesium sulphate. After filtering and concentrating the solution in a water-jet vacuum and drying in vacuo, 11.54 g of crude product were obtained in the form of a tacky oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710178B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-0efebf0306204be49d7b2753b8d39b9e
Quellennotizuspto-grants-2004_03