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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766038Generated: October 30, 2026

Urea → 5-(2-chloro-3-methoxyphenyl)pyrimidine-2,4(1H,3H)-dione

https://huagongshe.com/reaction/1766038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 2-(2-chloro-3-methoxyphenyl)-3-(dimethylamino)acrylateHCID 76539495—
SolventAcetonitrileHCID 6342—
Product5-(2-chloro-3-methoxyphenyl)pyrimidine-2,4(1H,3H)-dioneHCID 2203783582%

Reaction Steps

To a mixture of ethyl 2-(2-chloro-3-methoxyphenyl)-3-(dimethylamino)acrylate 3d (1.7 g, 6 mmol), urea (1.08 g, 18 mmol) and NaI (2.7 g, 18 mmol) in acetonitrile (20 mL) was added TMSCl (2.3 mL, 18 mmol). The resulting mixture was refluxed for 16 hours, cooled to room temperature, and 1.0 M NaOH (30 mL) was added. The resultant solution was stirred for 20 hours, and acetonitrile was removed in vacuo. The aq. solution was washed with ether, cooled in ice bath, and neutralized with 1 N HCl (30 mL). The precipitate was filtered, washed with additional H2O, and dried to give 5-(2-chloro-3-methoxyphenyl)pyrimidine-2,4(1H,3H)-dione 3e (1.24 g, 82%) as a pale yellow solid. MS (CI) m/z 253.1, 255.1 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229995B2
Source datasetuspto-grants-2007_06
ORD IDord-26d22f5e36844b0fb4cb36eff4b61b7c
Source noteuspto-grants-2007_06