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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369964Generated: October 26, 2026

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

https://huagongshe.com/reaction/1369964

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 numberUS06579984B1
Source datasetuspto-grants-2003_06
ORD IDord-a88c99e6b92846ce873a7ea338fac563
Source noteuspto-grants-2003_06