HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788043Generated: October 28, 2026
Water → 4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinone
https://huagongshe.com/reaction/1788043
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | 2,2,2-trichloro-N-[2-(3-chlorobenzoyl)-4-(4-fluorobenzoyl)phenyl]-acetamide | HCID 68688854 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinone | HCID 68690751 | 72.4% |
Reaction Steps
Acetic acid, ammonium salt (0.135 mol) was added at room temperature to a mixture of intermediate 4 (0.0675 mol) in DMSO (300 ml). The mixture was stirred at 60° C. for 4 hours, then brought to room temperature and poured out into water. The precipitate was filtered, washed with water, taken up in warm CH3CN, filtered, washed again with CH3CN, then with diethyl ether and dried under a vacuo, yielding 18.5 g (72%) of intermediate 5. The mother layer was purified by column chromatography over silica gel (15-40 μm) (eluent: DCM/MeOH:NH4OH 95/5/0.1). The pure fractions were collected and the solvent was evaporated. The residue was crystallized from 2-propanone/diethyl ether. The precipitate was filtered off and dried, yielding 1.8 g (7%) of 4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinone (intermediate 5), mp. 226° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07511138B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-4053017f320e42749ffe11e63cb6b74b |
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| Source note | uspto-grants-2009_03 |
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