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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626723Generated: October 31, 2026

Phosphorus oxybromide → 4-Bromo-2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine

https://huagongshe.com/reaction/626723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
Reactant2-(2,6-Dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine 5-oxideHCID 69671251—
Solvent1,2-DichloroethaneHCID 11—
Product4-Bromo-2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridineHCID 8669705631%

Reaction Steps

To a cooled (0° C.) solution of 2-(2,6-dichlorophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine 5-oxide (2.5 g, 8.4 mmol) in DCE (55 mL) under nitrogen was added phosphorous oxybromide (7.2 g, 25.2 mmol). The reaction mixture was stirred for 30 minutes, warmed to room temperature, and stirred for a further 4 hours. The reaction was quenched with sodium carbonate (sat. aq.) and the layers were partitioned. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (20% ethyl acetate in cyclohexane) to afford the title compound as a white solid (927 mg, 31% yield). LCMS (Method D): RT=3.74 min, m/z: 360 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309240B2
Source datasetuspto-grants-2016_04
ORD IDord-71bec91de8444363bf5f195eada85db9
Source noteuspto-grants-2016_04