HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897035Generated: October 30, 2026
Phosphorus pentachloride → HCID 10542881, compound
https://huagongshe.com/reaction/897035
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | HCID 12088011 | HCID 12088011 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | HCID 10542881 | HCID 10542881 | — |
Reaction Steps
A suspension of 265 mg (0.87 mmol) of 3-(2-chloro-phenyl)-6-fluoro-2-thioxo-2,3-dihydro-1H-quinazolin-4-one in 2.0 mL of POCl3 was treated with 300 mg of PCl5 and the mixture was refluxed for 2.5 hours. The solvent was evaporated and the residues were taken up in ethyl acetate, washed with water and brine, and then the solvent was evaporated to give 2-chloro-3-(2-chloro-phenyl)-6-fluoro-3H-quinazolin-4-one as a solid. This material was dissolved in 10 mL of absolute ethanol and 216 mg ( 1.73 mmol) of 2-fluorobenzylamine and the mixture was refluxed overnight. The reaction mixture was cooled and the solvent was evaporated. The residues were partitioned between ethyl acetate and dilute HCl and the aqueous phase was extracted further with ethyl acetate. The combined organic extracts were dried with brine and with magnesium sulfate (MgSO4) and evaporated to give a gum which was crystallized from ether to give 157 mg (45%) of the desired product, m.p. 163-165° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921764B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-1e60f911b7b948af890969999b473210 |
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| Source note | uspto-grants-2005_07 |
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