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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 965633Generated: October 29, 2026

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

https://huagongshe.com/reaction/965633

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 numberUS06951858B2
Source datasetuspto-grants-2005_10
ORD IDord-78f9c3be1f074e14a6b87f76a9b6e296
Source noteuspto-grants-2005_10