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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843648Generated: October 26, 2026

Water → 2-[3-(2-Chlorophenyl)-6-fluoro-4-oxo-3,4-dihydroquinazolin-2-yl-vinyl)pyridine-2-carbaldehyde

https://huagongshe.com/reaction/843648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,4-DioxaneHCID 31275—
Reactant4(3H)-Quinazolinone, 3-(2-chlorophenyl)-6-fluoro-2-methyl-HCID 64065—
Reactant2,6-DiformylpyridineHCID 79485—
CatalystZincchlorideHCID 3007855—
SolventAcetic AnhydrideHCID 7918—
Product2-[3-(2-Chlorophenyl)-6-fluoro-4-oxo-3,4-dihydroquinazolin-2-yl-vinyl)pyridine-2-carbaldehydeHCID 86583867—

Reaction Steps

A catalytic amount (about 100 mg) of anhydrous zinc chloride was added to a solution of 576 mg (2.0 mmol) of 3-(2-chlorophenyl)-6-fluoro-2-methyl-4(3H)-quinazolinone and 270 mg (2.0 mmol) of 2,6-pyridinedicarboxaldehyde in 20-25 mL of dioxane and 1.0 mL of acetic anhydride. The reaction mixture was heated at reflux under a nitrogen atmosphere for 3 hours until TLC indicated that the starting materials had been consumed. The cooled reaction mixture was poured into water and the mixture was extracted with ethyl acetate. The combined extracts were dried with brine and magnesium sulfate, treated with decolonizing carbon and filtered and the solvent was removed to give the desired product. This was taken up in 2:1 ether/pentane and the crystals were filtered to give 266 mg of the product, 33%, m.p. 247-248° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380204B1
Source datasetuspto-grants-2002_04
ORD IDord-e414f10c31ef4c24873d9551f513cbb0
Source noteuspto-grants-2002_04