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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629890Generated: November 1, 2026

Hydrogen Peroxide → HCID 71140744, compound

https://huagongshe.com/reaction/629890

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantBorane;tetrahydrofuranHCID 2723981—
ReactantHCID 71135237HCID 71135237—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 71140744HCID 71140744—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a round bottom flask was added tert-butyl 3-[1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl]-8-azabicyclo[3.2.1]oct-2-ene-8-carboxylate (17-31) (1.5 g, 3.52 mmol), and anhydrous THF (15 mL). The reaction mixture was then cooled to 0° C. under an atmosphere of nitrogen, and added borane tetrahydrofuran COMPLEX (1M in THF) (3.87 ml, 3.87 mmol) dropwise over 10 minutes while stirring. Stirred for ˜10 minutes, then permitted to warm to room temperature for 30 minutes. Next cooled back to 0° C. and uncapped, and when open to atmosphere added hydrogen peroxide(35% by wt in H2O) (1.539 ml, 17.58 mmol) & sodium hydroxide (1M in H2O) (8.79 mL, 8.79 mmol) slowly over 20 minutes, then warmed to room temperature. The reaction was then permitted to stir overnight at room temperature (16 hours), then suspended in EtOAc, washed with a saturated solution of Na2S2O3, then saturated NaHCO3, followed by water and brine, dried over Na2SO4, filtered and concentrated. The resulting residue was purified by silica gel chromatography (0-100% EtOAc/Hex) to yield tert-Butyl 3-[1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo-[4,5-b]pyridin-5-yl]-2-hydroxy-8-azabicyclo[3.2.1]octane-8-carboxylate (20-1). HRMS (M+H)+: observed=429.2865, calculated=429.2860.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315518B2
Source datasetuspto-grants-2016_04
ORD IDord-6db0a8d24e644a408291784ae2e983ce
Source noteuspto-grants-2016_04