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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Pyrosulfite | HCID 656671 | — |
| Reactant | Ammonium cerium-nitrate | HCID 57418452 | — |
| Reactant | N-{[6-bromo-1-(4-methoxybenzyl)-2-oxo-4-(trifluoromethyl)-1,2,3,4-tetrahydroquinazolin-4-yl]methyl}-4-fluorobenzamide | HCID 68486610 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-{[6-bromo-2-oxo-4-(trifluoromethyl)-1,2, 3,4-tetrahydroquinazolin-4-yl]methyl}-4-fluorobenzamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314094B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-7601f1823f774a5ea3a1dccd066bb013 |
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| Source note | uspto-grants-2012_11 |
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