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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 566189Generated: November 1, 2026

HCID 2166334, compound → HCID 21265538, compound

https://huagongshe.com/reaction/566189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2166334HCID 2166334—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 15858722HCID 15858722—
SolventDimethylformamideHCID 6228—
ProductHCID 21265538HCID 2126553842.6%

Reaction Conditions

Temperature5 °C

Reaction Steps

Ethyl 3-amino-4,4,4-trifluoro-2-methylcrotonate (26.0 g) was dissolved in DMF (123 ml). To this solution, a suspension of sodium methoxide in DNF (7.78 g) was added dropwise at 0° C., and the mixture was stirred at 5° C. for 30 minutes. Then, a DMF solution of ethyl N-(4-bromo-2-fluoro-phenyl)carbamate (31.44 g) was added dropwise thereto, and the mixture was stirred at 130° C. for 5 hours. After the reaction, DMF was distilled off under reduced pressure, and the residue was acidified by adding diluted hydrochloric acid thereto. This was extracted with ethyl acetate, washed with water, and then dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off, and the resulting residue was crystallized from ethyl acetate-n-hexane (1:3 v/v) to obtain the objective 3-(4-bromo-2-fluorophenyl)-5-methyl-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione (18.78 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06174839B1
Source datasetuspto-grants-2001_01
ORD IDord-97229743c1c04a3ca01a9325971d6085
Source noteuspto-grants-2001_01