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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2193032Generated: November 1, 2026

Methyl morpholine oxide → 1-(1-Butoxy-9-fluorobenzo[c]-1,6-naphthyridin-6-yl)ethanone

https://huagongshe.com/reaction/2193032

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 59375395HCID 59375395—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Butoxy-9-fluorobenzo[c]-1,6-naphthyridin-6-yl)ethanoneHCID 59375541—

Reaction Steps

To a stirred solution of 1-butoxy-9-fluoro-6-isopropenylbenzo[c]-1,6-naphthyridine (100 mg, 0.320 mmol) in tetrahydrofuran (1.0 ml) and water (0.25 ml) was added 4-methylmorpholine 4-oxide (NMO) (39.6 mg, 0.338 mmol) followed by osmium tetroxide (525 uL of a 4 wt % aqueous solution. The reaction mixture was stirred at room temperature for 1 hr. Additional tetrahydrofuran (1.0 ml) and water (0.25 ml) were added, followed by an additional portion of NMO (39.6 mg, 0.338 mmol). The reaction mixture was partitioned between EtOAc and water. The organic layer was dried over sodium sulfate, filtered, and concentrated to a crude residue that was adsorbed on to silica gel and purified by silica gel chromatography eluting with an EtOAc/hexanes gradient to afford 1-(1-butoxy-9-fluorobenzo[c]-1,6-naphthyridin-6-yl)ethanone. LRMS (ESI) calc'd for (C18H17FN2O2) [M+H]+, 313.1; found 313.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329722B2
Source datasetuspto-grants-2012_12
ORD IDord-1e4195eca2614cf49a032c5f7d7f13b6
Source noteuspto-grants-2012_12