Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50107Generated: October 25, 2026

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

https://huagongshe.com/reaction/50107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantN-cyano-N-methylmethanesulphonamideHCID 10219456—
ReactantHCID 178500902HCID 178500902—
CatalystTitanium TetrachlorideHCID 24193—
SolventWaterHCID 962—
ProductMethyl 4-(4-fluorophenyl)-6-(1-methylethyl)-2-(methyl(methylsulfonyl)amino)-5-pyrimidinecarboxylateHCID 992982180.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710178B2
Source datasetuspto-grants-2004_03
ORD IDord-0efebf0306204be49d7b2753b8d39b9e
Source noteuspto-grants-2004_03