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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587356Generated: October 27, 2026

Methyl iodide → 4-methyl-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-3-one

https://huagongshe.com/reaction/1587356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant2H-pyrido(3,2-b)-1,4-oxazin-3(4H)-oneHCID 88499—
SolventDimethylformamideHCID 6228—
Product4-methyl-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-3-oneHCID 15537451—

Reaction Steps

2,3-Dihydro-4H-pyrido[3,2-b][1,4]oxazin-3-one (U.S. Pat. No. 3,854,926; 1.5 g) was added portionwise to a stirred suspension of sodium hydride (60% w/w dispersion in mineral oil; 0.4 g) in DMF (30 ml) which had been cooled in an ice-bath. The mixture was allowed to warm to ambient temperature and was stirred for 30 minutes. Methyl iodide (0.65 ml) was added and the mixture was stirred at ambient temperature for 16 hours. The mixture was poured into a saturated aqeuous ammonium chloride solution and extracted with ethyl acetate. The organic phase was washed with water and with brine, dried (MgSO4) and evaporated to give 4-methyl-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-3-one (1.58 g) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05217969
Source datasetuspto-grants-1993_06
ORD IDord-cc36d6185802493f8e08fd2a2dd3cbba
Source noteuspto-grants-1993_06