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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantPyrido[2,3-b][1,4]benzoxazepin-6(5H)-oneHCID 11820483—
Reactant(Dimethyl sulfide)trihydroboronHCID 12423031—
SolventTetrahydrofuranHCID 8028—
Product5,6-Dihydropyrido[2,3-b][1,4]benzoxazepineHCID 2209981629.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849735
Source datasetuspto-grants-1998_12
ORD IDord-55f29b6ea60848ad846c6240871851de
Source noteuspto-grants-1998_12