HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788044Generated: October 29, 2026
Phosphorus oxychloride → [2-Chloro-4-(3-chlorophenyl)-6-quinazolinyl](4-fluorophenyl)-methanone
https://huagongshe.com/reaction/1788044
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 4-(3-chlorophenyl)-6-(4-fluorobenzoyl)-2(1H)-quinazolinone | HCID 68690751 | — |
| Product | [2-Chloro-4-(3-chlorophenyl)-6-quinazolinyl](4-fluorophenyl)-methanone | HCID 17976100 | 40% |
Reaction Steps
Intermediate 5 (0.0528 mol) was added in phosphoryl chloride (200 ml) at room temperature. The mixture was stirred at 100° C. for 3 hours and cooled to room temperature. The solvent was evaporated. The residue was taken up in DCM. The solvent was evaporated till dryness. The residue was taken up in DCM, poured out into ice water, neutralised with K2CO3 solid and extracted with DCM. The organic layer was washed with water, separated, dried (MgSO4), filtered, and the solvent was evaporated. The residue was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 8.5 g (40%) of intermediate 6. The mother layer was evaporated. The residue was purified by column chromatography over silica gel (eluent: toluene/EtOAc 95/5; 15-35 μm). The pure fractions were collected and the solvent was evaporated. A part (0.5 g) of the residue (8.9 g, 42%) was crystallized from 2-propanone. The precipitate was filtered off and dried, yielding 0.3 g of [2-chloro-4-(3-chlorophenyl)-6-quinazolinyl](4-fluorophenyl)-methanone (intermediate 6), mp. 138° 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-811dcd1b6fb74c07ae99ce1c64a9a47d |
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| Source note | uspto-grants-2009_03 |
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