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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-bromo-1H,2H,3H-pyrido[2,3-b][1,4]oxazin-2-one | HCID 4590141 | — |
| Catalyst | Benzyl triethylammonium chloride | HCID 66133 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-bromo-1-methyl-1H-pyrido[2,3-b][1,4]oxazin-2(3H)-one | HCID 66890084 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08604050B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-976705de58f8482bbffe4ac62684584e |
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| Source note | uspto-grants-2013_12 |
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