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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985465Generated: October 26, 2026

5-Bromouracil → Urea, (2,6-difluorobenzyl)-

https://huagongshe.com/reaction/985465

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromouracilHCID 5802—
Reactant2-(Bromomethyl)-1,3-difluorobenzeneHCID 581435—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
Solvent1,1-DichloroethaneHCID 6365—
ProductUrea, (2,6-difluorobenzyl)-HCID 20528284.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 5-bromouracil (18.45 g, 96.6 mmol) in 300 mL of dichloroethane was treated with N,O-bis(trimethylsilyl)acetamide (48 mL, 39.5 g, 194 mmol). The reaction mixture was heated at 80° C. for 3 hr under the nitrogen. The solution was cooled down to ambient temperature, 2,6-difluorobenzyl bromide (25 g, 120 mmol) was added and the reaction mixture was heated at 80° C. overnight under the protection of nitrogen. The reaction was cooled down, quenched with MeOH (15 mL), and partitioned between dichloromethane (500 mL) and water (250 mL). The organic layer was washed with brine, dried (sodium sulfate), and evaporated to give a solid. The crude product was triturated with ether, filtered, and washed with ether three times to give compound 1 (15.2 g, 50%) as a white solid; MS (CI) m/z 316.90, 318.90 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872728B2
Source datasetuspto-grants-2005_03
ORD IDord-ebe24909ddcb4ff782716f74717acbd6
Source noteuspto-grants-2005_03