HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-methyl-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2H-pyrido(3,2-b)-1,4-oxazin-3(4H)-one | HCID 88499 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-methyl-2,3-dihydro-4H-pyrido[3,2-b][1,4]oxazin-3-one | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05217969 |
| Source dataset | uspto-grants-1993_06 |
| ORD ID | ord-cc36d6185802493f8e08fd2a2dd3cbba |
| Source note | uspto-grants-1993_06 |