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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270423Generated: 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/2270423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Ethyl-2-methylpyridineHCID 7728—
ReactantSodium CyanideHCID 8929—
ReactantSodium hydrideHCID 24758—
Reactant3-(4-bromo-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)pyrimidinedioneHCID 10874406—
CatalystCupric ChlorideHCID 24014—
CatalystHCID 178418397HCID 178418397—
Product3-(4-cyano-5-ethylsulfonylamino-2-fluorophenyl)-1-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedioneHCID 1109107779%

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 and 0.11 g of 55% sodium hydride in oil were added to 20 g of 5-ethyl-2-picoline and the mixture was stirred at room temperature for 30 minutes. Next, 0.07 g of copper(II) chloride and 0.15 g of sodium cyanide were added to the mixture, which was then stirred at 140° C. under an argon atmosphere for 1 hour. Further, 0.3 g of tetrakis(triphenylphosphine)palladium was added to the mixture, which was then heated with stirring for 3 hours. After the reaction was completed, 79% of the title compound was detected as the relative area value in liquid chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331628B1
Source datasetuspto-grants-2001_12
ORD IDord-f7c4ce6c50644725bd9d7572e33eaeea
Source noteuspto-grants-2001_12