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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838107Generated: November 3, 2026

6-phenyl-1,2,4-triazine-3,5(2h,4h)-dione → HCID 22313051, compound

https://huagongshe.com/reaction/1838107

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-phenyl-1,2,4-triazine-3,5(2h,4h)-dioneHCID 253363—
Reactant2-(Bromomethyl)-1,3-difluorobenzeneHCID 581435—
ReactantBistrimethylsilylacetamidHCID 11708267—
SolventAcetonitrileHCID 6342—
ProductHCID 22313051HCID 2231305188.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring suspension of 6-phenyl-1,2,4-triazine-3,5-(2H,4H)-dione (6.00 g, 31.7 mmol) in dry acetonitrile (50 mL) under nitrogen was added bis(trimethylsilyl)acetamide (15.7 mL, 63.4 mmol). The resulting yellow solution was heated at 80° C. for 3 hours. The solution was cooled and 2,6-difluorobenzyl bromide (8.20 g, 39.6 mmol) was added in one portion. The mixture was heated at 80° C. under nitrogen for an additional 15 hours. The resulting solution was cooled to room temperature, quenched with methanol (20 mL), and diluted with dichloromethane (175 mL). The mixture was washed with water (75 mL) and brine (70 mL), and dried over magnesium sulfate. Evaporation gave a tan solid that was triturated with cold diethyl ether (5×5 mL). After drying in vacuo, the compound was isolated as a flocculent, off-white solid (8.80 g, 88%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06673796B2
Source datasetuspto-grants-2004_01
ORD IDord-cb9b50b117234d708bff4598fd6c1602
Source noteuspto-grants-2004_01