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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878033Generated: November 3, 2026

Sodium Pyrosulfite → N-{[6-bromo-2-oxo-4-(trifluoromethyl)-1,2, 3,4-tetrahydroquinazolin-4-yl]methyl}-4-fluorobenzamide

https://huagongshe.com/reaction/1878033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium PyrosulfiteHCID 656671—
ReactantAmmonium cerium-nitrateHCID 57418452—
ReactantN-{[6-bromo-1-(4-methoxybenzyl)-2-oxo-4-(trifluoromethyl)-1,2,3,4-tetrahydroquinazolin-4-yl]methyl}-4-fluorobenzamideHCID 68486610—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
ProductN-{[6-bromo-2-oxo-4-(trifluoromethyl)-1,2, 3,4-tetrahydroquinazolin-4-yl]methyl}-4-fluorobenzamideHCID 68488834—

Reaction Steps

To a stirring solution of N-{[6-bromo-1-(4-methoxybenzyl)-2-oxo-4-(trifluoromethyl)-1,2,3,4-tetrahydroquinazolin-4-yl]methyl}-4-fluorobenzamide (260 mg, 0.46 mmol) in acetonitrile (6 mL), an aqueous solution (1 mL) of cerium ammonium nitrate (755 mg, 1.38 mmol) was added dropwise at room temperature. The reaction solution was stirred at room temperature for 4 hours. Sodium pyrosulfite was added to the reaction solution, and the solution was stirred for 30 minutes, and then diluted with ethyl acetate and the organic layer was separated. The organic layer was washed sequentially with water and saturated brine and then dried over magnesium sulfate. After the drying agent was removed by filtration, the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=2/1), whereby the objective compound (150 mg, 73%) was obtained as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08314094B2
Source datasetuspto-grants-2012_11
ORD IDord-7601f1823f774a5ea3a1dccd066bb013
Source noteuspto-grants-2012_11