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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878025Generated: November 2, 2026

Ethanol → HCID 136337197, compound

https://huagongshe.com/reaction/1878025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 68490661HCID 68490661—
SolventHydroxylamineHCID 787—
SolventEthyl AcetateHCID 8857—
ProductHCID 136337197HCID 136337197—

Reaction Steps

To a solution of N-{[6-cyano-2-oxo-4-(trifluoromethyl)-1,4-dihydro-2H-3,1-benzoxazin-4-yl]methyl}-4-fluorobenzamide (50 mg, 0.127 mmol) synthesized in Example 159 in ethanol (0.5 mL), hydroxylamine (50% aqueous solution, 40 μL) was added, and the solution was stirred overnight at room temperature. The solution was diluted with ethyl acetate, which was washed sequentially with water and saturated brine and then dried over magnesium sulfate. The residue was dissolved in dioxane (1 mL), and under stirring the solution at room temperature, CDI (41 mg, 0.25 mmol) was added thereto. After the reaction solution was stirred at 90° C. for 3 hours, the temperature of the solution was brought to room temperature. Then, the solution was diluted with ethyl acetate, which was washed sequentially with water, 1 N hydrochloric acid and saturated brine and then dried over magnesium sulfate. After the drying agent was removed by filtration, the residue was crystallized with ethanol and water, whereby the objective compound (18 mg, 31%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314094B2
Source datasetuspto-grants-2012_11
ORD IDord-44b07d08068442acbaebe13e2cd6fbf5
Source noteuspto-grants-2012_11