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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1911244Generated: October 30, 2026

Methyl iodide → 7-bromo-1-methyl-1H-pyrido[2,3-b][1,4]oxazin-2(3H)-one

https://huagongshe.com/reaction/1911244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant7-bromo-1H,2H,3H-pyrido[2,3-b][1,4]oxazin-2-oneHCID 4590141—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventAcetonitrileHCID 6342—
Product7-bromo-1-methyl-1H-pyrido[2,3-b][1,4]oxazin-2(3H)-oneHCID 66890084—

Reaction Conditions

Temperature60 °C

Reaction Steps

0.16 mL (2.62 mmol) of methyl iodide is added to a suspension of 0.5 g (2.18 mol) of 7-bromo-2-oxo-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine, 0.24 g (1.09 mmol) of benzyltriethylammonium chloride and 0.75 g (5.46 mmol) of potassium carbonate in 25 mL of acetonitrile. The mixture is stirred for 6 hours at 60° C. After this time, a precipitate is removed by filtration. The filtrate is concentrated under reduced pressure and the resulting solid is taken up in 15 mL of dichloromethane and then washed successively with 20 ml of water, 10 mL of 0.1N hydrochloric acid solution, 10 mL of saturated sodium hydrogen carbonate solution and then 10 mL of water. After drying over sodium sulfate, the solution is finally concentrated under reduced pressure to give the expected product, which is used without further purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604050B2
Source datasetuspto-grants-2013_12
ORD IDord-976705de58f8482bbffe4ac62684584e
Source noteuspto-grants-2013_12