HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943751Generated: October 27, 2026
Water → 5-methyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine
https://huagongshe.com/reaction/1943751
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | 5-methyl-1H-pyrido[2,3-b][1,4]oxazin-2-one | HCID 66936755 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-methyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine | HCID 66936530 | 50% |
Reaction Steps
5-methyl-1H-pyrido[2,3-b][1,4]oxazin-2-one (1.5 g, 9.1 mmol) was dissolved in 20 ml of anhydrous tetrahydrofuran under nitrogen atmosphere, and then cooled to 0° C. 1.0M Lithium aluminum hydride dissolved in tetrahydrofuran (11 ml, 10.9 mmol) was added thereto dropwise and then stirred for 30 minutes. The reaction temperature was raised to room temperature and stirred for 1 hour. The reaction mixture was cooled to 0° C. again and water (0.3 ml), 10% sodium hydroxide solution (0.6 ml) and water (0.9 ml) were added thereto dropwise in this order, and then stirred vigorously at room temperature for 1 hour. The formed solid was filtered and washed with excess ethyl acetate. The filtrate was washed with water and saturated saline solution, dried over anhydrous sodium sulfate (Na2SO4), filtered and evaporated under reduced pressure to obtain 5-methyl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine as white solid (680 mg, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394792B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-21fa28eeeb41456a8b52afae835c60c3 |
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| Source note | uspto-grants-2013_03 |
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