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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270422Generated: October 31, 2026

5-Ethyl-2-methylpyridine → 3-(4-cyano-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione

https://huagongshe.com/reaction/2270422

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Ethyl-2-methylpyridineHCID 7728—
ReactantSodium CyanideHCID 8929—
Reactant3-(4-bromo-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)pyrimidinedioneHCID 10874406—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
Product3-(4-cyano-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedioneHCID 1109107790%

Reaction Conditions

Temperature120 °C

Reaction Steps

1.2 g (2.5 mmol) of 3-(4-bromo-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)pyrimidinedione, 0.15 g of sodium cyanide and 0.04 g of zinc chloride were added to 5 ml of 5-ethyl-2-picoline and the mixture was stirred at 120° C. under an argon atmosphere for 1 hour. Next, 0.6 g of tetrakis(triphenylphosphine)palladium was added to the mixture, which was then heated with stirring for 10 hours. After the reaction was completed, the title compound was obtained with a yield of 90% as determined by the internal standard method in liquid chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331628B1
Source datasetuspto-grants-2001_12
ORD IDord-d449805504fe487589eb35effe714105
Source noteuspto-grants-2001_12