HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 381274Generated: November 3, 2026
HCID 54544936, compound → HCID 18362995, compound
https://huagongshe.com/reaction/381274
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 54544936 | HCID 54544936 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 18362995 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06306864B1 |
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| Source dataset | uspto-grants-2001_10 |
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| ORD ID | ord-be68ff40883f426a8b416c4916743d6b |
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| Source note | uspto-grants-2001_10 |
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