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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473143Generated: October 26, 2026

Ethyl Acetate → HCID 178517774, compound

https://huagongshe.com/reaction/473143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-Amino-4-bromobenzamideHCID 13805507—
ReactantTrimethyl(phosphooxy)silaneHCID 16133246—
ReactantSodium 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetateHCID 66609989—
SolventWaterHCID 962—
ProductHCID 178517774HCID 17851777477%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a mixture of sodium 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetate from Example 2 Step B (2.05 g, 9.62 mmol) and 2-amino-4-bromobenzamide (1.89 g, 8.75 mmol) was added trimethylsilyl polyphosphate (˜15 mL) and the mixture was stirred overnight at 120° C. Equal volumes of EtOAc and water were added and the resulting solution was stirred for 1 h. The EtOAc layer was washed with brine, dried over Na2SO4 and then concentrated under reduced pressure. Et2O was added and evaporated. Trituration of the residue with hexanes, followed by collection of the solid by filtration afforded 7-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)quinazolin-4-ol (2.49 g, 77%). 1H NMR (300 MHz, DMSO-d6) δ 11.37 (s, 1H), 8.76 (s, 1H), 7.97-8.07 (m, 2H), 7.88 (d, J=8.3 Hz, 1H), 7.69-7.81 (m, 2H);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633207B2
Source datasetuspto-grants-2014_01
ORD IDord-892dd47a47fb4d819fccf96d561ff847
Source noteuspto-grants-2014_01