HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943704Generated: November 2, 2026
Water → 7-pyridin-3-yl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine
https://huagongshe.com/reaction/1943704
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 | 7-pyridin-3-yl-1H-pyrido[2,3-b][1,4]oxazin-2-one | HCID 66936747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 7-pyridin-3-yl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine | HCID 66936892 | 53.3% |
Reaction Steps
7-pyridin-3-yl-1H-pyrido[2,3-b][1,4]oxazin-2-one (60 mg, 0.264 mmol) was dissolved in 4 ml of anhydrous tetrahydrofuran under nitrogen atmosphere, and the mixture was cooled to 0□, and 1.0M Lithium aluminum hydride dissolved in tetrahydrofuran (0.7 ml, 0.704 mmol) was added thereto dropwise at room temperature for 5 hours. To the reaction mixture, water (0.3 ml), 10% sodium hydroxide (0.6 ml) and water (0.9 ml) were added 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 Na2SO4, filtered and evaporated under reduced pressure to obtain 7-pyridin-3-yl-2,3-dihydro-1H-pyrido[2,3-b][1,4]oxazine as white solid (30 mg, 53%).
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-03b2d08e267e4f238b59d3b8037c19ec |
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| Source note | uspto-grants-2013_03 |
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