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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381274Generated: November 3, 2026

HCID 54544936, compound → HCID 18362995, compound

https://huagongshe.com/reaction/381274

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 54544936HCID 54544936—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductHCID 18362995HCID 18362995—

Reaction Steps

A solution of 1.00 gram (2.65 mmol) of 3-(2-Chloro-phenyl)-6-fluoro-2-(2-pyridin-2-yl-vinyl)-3H-quinazolin-4-one in about 100 mL of ethyl acetate was treated with 0.5 gram of 10% Pd/C and the resulting mixture was hydrogenated at about 2 cm of Hg for two hours at which time uptake of hydrogen had ceased. The catalyst was filtered off with the aid of supercel (filteraid) and the ethyl acetate was removed by evaporation. The residues were dissolved in diethyl ether and treated with excess of a solution of HCl gas in diethyl ether. The product precipitated immediately and was allowed to stir for 3 hours at which time it was separated by filtration and dried in a stream of dry nitrogen. The product was 1.15 g (100%) of 3-(2-chloro-phenyl)-6-fluoro-2-(2-pyridin-2-yl-ethyl)-3H-quinazolin-4-one hydrochloride, an amorphous white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06306864B1
Source datasetuspto-grants-2001_10
ORD IDord-be68ff40883f426a8b416c4916743d6b
Source noteuspto-grants-2001_10