HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457651Generated: October 26, 2026
Methanol → 5,6-Dihydropyrido[2,3-b][1,4]benzoxazepine
https://huagongshe.com/reaction/1457651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyrido[2,3-b][1,4]benzoxazepin-6(5H)-one | HCID 11820483 | — |
| Reactant | (Dimethyl sulfide)trihydroboron | HCID 12423031 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5,6-Dihydropyrido[2,3-b][1,4]benzoxazepine | HCID 22099816 | 29.8% |
Reaction Steps
A mixture of 2.8 g of pyrido[2,3-b][1,4]benzoxazepin-6(5H)-one, 10 ml of tetrahydrofuran and 3 ml of 10M borane-dimethylsulfide in tetrahydrofuran is stirred at room temperature overnight and then refluxed for 3 hours. To the mixture is added dropwise under argon, 5 ml of methanol. The solvent is removed under vacuum and methanol added. The solvent is removed under vacuum and 12 ml of 2N NaOH added to the residue. The mixture is refluxed for 2 hours and extracted with ethyl acetate. The extract is washed with 2N citric acid, H2O, brine and dried (Na2SO4). The solution is filtered through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness under vacuum. The residue is chromatographed on a column (2"×18") of silica gel (32° g) with hexane-ethyl acetate (1:1) as solvent to give 0.78 g of crystals, m.p. 172°-174° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05849735 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-55f29b6ea60848ad846c6240871851de |
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| Source note | uspto-grants-1998_12 |
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