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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053167Generated: October 31, 2026

Hydrogen Bromide → 4-chloro-2,5-difluoro-N-(2-oxo-1H-pyridin-4-yl)benzamide

https://huagongshe.com/reaction/1053167

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantWaterHCID 962—
Reactant4-chloro-2,5-difluoro-N-(2-methoxy-4-pyridyl)benzamideHCID 86728480—
SolventAcetic AcidHCID 176—
Product4-chloro-2,5-difluoro-N-(2-oxo-1H-pyridin-4-yl)benzamideHCID 8672848134%

Reaction Conditions

Temperature90 °C

Reaction Steps

To 4-chloro-2,5-difluoro-N-(2-methoxy-4-pyridyl)benzamide (3 g, 10.04 mmol) in HOAc (15.9 mL) was added HBr 33% in HOAc (12.31 mL of 33% w/v, 50.20 mmol) and the mixture was stirred at 90° C. for 5 h. Additional HBr (10 mL, 33% in HOAc) was added and the mixture was stirred at 90° C. overnight. The mixture was cooled to room temperature and was poured into water (100 mL). The mixture was stirred and the solid was collected by filtration. The solid was washed with water (2×50 mL). The solid was slurried in hexanes (2×50 mL) and filtered to give 4-chloro-2,5-difluoro-N-(2-oxo-1H-pyridin-4-yl)benzamide (969.7 mg, 34%) as a cream colored solid. ESI-MS m/z calc. 284.02. found 285.3 (M+1)+; Retention time: 1.36 minutes (3 min run).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09393235B2
Source datasetuspto-grants-2016_07
ORD IDord-b15e393daca9491fb14550495679d421
Source noteuspto-grants-2016_07