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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445724Generated: October 31, 2026

Methyl iodide → 6-Bromo-1-methyl-1,4-dihydro-pyrido[2,3-d][1,3]oxazin-2-one

https://huagongshe.com/reaction/445724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant6-bromo-1H,2H,4H-pyrido(2,3-d)(1,3)oxazin-2-oneHCID 15925990—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-Bromo-1-methyl-1,4-dihydro-pyrido[2,3-d][1,3]oxazin-2-oneHCID 59619719—

Reaction Steps

To a solution of 6-bromo-1,4-dihydro-pyrido[2,3-d][1,3]oxazin-2-one (Stage 170.1.3, 0.707 mmol) in DMF (1.4 ml) was added 55% sodium hydride in oil (0.778 mmol). The RM was stirred for 5 min at rt then was added iodomethane (0.778 mmol) and the RM was stirred for 30 min at rt. The RM was diluted with EtOAc, washed with saturated NaHCO3, with brine (3×), dried over Na2SO4, filtered and evaporated. The residue was absorbed on silica gel and separated by flash chromatography (heptane/EtOAc 0% to 70%). The fractions containing product were evaporated together to give the title compound as a yellow solid. (HPLC: tR 2.64 min (Method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476294B2
Source datasetuspto-grants-2013_07
ORD IDord-82ea5e6779dc4a879124cd5e7fce1d0f
Source noteuspto-grants-2013_07