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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416469Generated: November 1, 2026

Acetone → HCID 67582894, compound

https://huagongshe.com/reaction/1416469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactanttert-ButanolHCID 6386—
ReactantMethyl morpholine oxideHCID 82029—
ReactantHCID 67582038HCID 67582038—
CatalystOsmium TetroxideHCID 30318—
SolventWaterHCID 962—
ProductHCID 67582894HCID 67582894—

Reaction Steps

A mixture of 2-[4-(benzyloxycarbonyl)piperazin-1-yl]-4-[(1S,4R)-(4-hydroxycyclopent-2-en-1-yl)oxy]quinazoline (1.30 g), a solution of osmium tetroxide in t-butanol (osmium tetroxide 252 mg/t-butanol 18.1 g) (532 mg) and 4-methylmorpholine N-oxide (375 mg) in water (3 ml)--acetone (25 ml) is stirred at room temperature for 17 hours. Acetone is distilled off from the reaction mixture under reduced pressure, and to the resultant is added ethyl acetate, and the mixture is washed with 10% aqueous sodium sulfite solution and water. The ethyl acetate solution is dried over anhydrous magnesium sulfate and evaporated to dryness under reduced pressure, and the residue is purified by medium pressure liquid column chromatography (eluent, chloroform:methanol=50:1, 10:1, v/v) to give 2-[4-(benzyloxycarbonyl) piperazin-1-yl]-4-[(1S,2S,3S,4R)-(2,3,4-trihydroxycyclopentan-1-yl)oxy]quinazoline (1.05 mg) as foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912247
Source datasetuspto-grants-1999_06
ORD IDord-406e7175fe7640168833f420db5495f4
Source noteuspto-grants-1999_06