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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381267Generated: 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/381267

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 numberUS06306864B1
Source datasetuspto-grants-2001_10
ORD IDord-94cc04b662cc4a358cdbe22d7fa356db
Source noteuspto-grants-2001_10