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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473162Generated: October 27, 2026

2-Amino-3-chlorobenzamide → 8-chloro-2-(difluoro(5-fluoropyridin-2-yl)methyl)quinazolin-4(3H)-one

https://huagongshe.com/reaction/473162

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-chlorobenzamideHCID 14100428—
ReactantSodium 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetateHCID 66609989—
SolventWaterHCID 962—
Product8-chloro-2-(difluoro(5-fluoropyridin-2-yl)methyl)quinazolin-4(3H)-oneHCID 13634059092.1%

Reaction Conditions

Temperature115 °C

Reaction Steps

Sodium 2,2-difluoro-2-(5-fluoropyridin-2-yl)acetate from Example 2 Step B (51 mg, 0.24 mmol) and 2-amino-3-chloro-benzamide (34 mg, 0.20 mmol) were combined with polyphosphoric acid (1.0 g) and the mixture was heated at 115° C. for 20 h with vigorous stirring. The mixture was allowed to cool to rt and then water (3 mL) was added, resulting in a precipitate that was separated washing with DCE (2×8 mL). The combined DCE extracts were washed with brine (3 mL) and separated using Biotage Phase Separators. The organic fraction was concentrated using a Savant Speed Vac to afford 8-chloro-2-(difluoro(5-fluoropyridin-2-yl)methyl)quinazolin-4(3H)-one as an off-white solid (60 mg). LCMS (ESI) m/z 326 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633207B2
Source datasetuspto-grants-2014_01
ORD IDord-4cb58f0eeab045728e2728b8257dc007
Source noteuspto-grants-2014_01