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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626732Generated: October 31, 2026

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

https://huagongshe.com/reaction/626732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
Reactant7-Bromo-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-5-oxideHCID 69671339—
Solvent1,2-DichloroethaneHCID 11—
Product4,7-Dibromo-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridineHCID 8669705954%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled (0° C.) suspension of 7-bromo-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-5-oxide (1.7 g, 4.7 mmol) in DCE (30 mL) was added phosphorus oxybromide (4.0 g, 14.1 mmol). The reaction mixture was stirred at 0° C. for 15 minutes, warmed to room temperature, and stirred for a further 2.25 hours. The reaction mixture was partitioned between DCM and sodium carbonate (sat. aq.). The organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel flash chromatography (0-20% ethyl acetate in cyclohexane) to afford the title compound as a white solid (1.07 g, 54% yield). LCMS (Method D): RT=3.93 min, m/z: 422 [M+H+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309240B2
Source datasetuspto-grants-2016_04
ORD IDord-a027bc24e37d4b9bb1ead1208a062348
Source noteuspto-grants-2016_04