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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929154Generated: October 30, 2026

Dichloromethane methanol → HCID 90042613, compound

https://huagongshe.com/reaction/929154

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethane methanolHCID 21226129—
ReactantSodium periodateHCID 23667635—
ReactantHCID 90042055HCID 90042055—
CatalystRuthenium trichloride hydrateHCID 6093376—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductHCID 90042613HCID 90042613—

Reaction Steps

Ruthenium(III) chloride hydrate (3.7 mg, 0.016 mmol) and sodium periodate (121.7 mg, 0.569 mmol) were added to a stirred solution of (3R,3aR,6R,6aS)-6-allyl-3-[[6-chloro-5-(4-phenylphenyl)-1H-imidazo[4,5-b]pyridin-2-yl]oxy]-3,3a,5,6a-tetrahydro-2H-furo[3,2-b]furan-6-ol (122.5 mg, 0.250 mmol) in acetonitrile (2.14 ml) and water (0.36 ml). The reaction mixture was stirred at room temperature for 3 h, then partitioned between EtOAc (75 ml) and saturated aqueous sodium thiosulfate (40 ml). The aqueous layer was extracted with EtOAc (2×50 ml). The organic layers were combined, washed with brine (1×30 ml), dried over MgSO4, filtered, and evaporated under reduced pressure to give a colorless residue. This material was dissolved in EtOAc and loaded onto three 500 micron 20 cm×20 cm silica gel plates, which were developed using 10% MeOH/DCM. The silica containing the product band was collected and eluted with 10% MeOH/DCM (80 ml). The solvent was evaporated under reduced pressure and the resulting residue was lyophilized from ethanol and benzene to give the title compound as a white solid. LC-MS: calculated for C26H22ClN3O5 491.12 observed m/e: 492.18 (M+H)+ (Rt 1.18/2 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-2c23aa47fcb347bfb4fb35fb445c60e2
Source noteuspto-grants-2016_03