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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | 7-Bromo-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine-5-oxide | HCID 69671339 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4,7-Dibromo-2-(2,6-dichlorophenyl)-2H-pyrazolo[4,3-c]pyridine | HCID 86697059 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309240B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-a027bc24e37d4b9bb1ead1208a062348 |
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| Source note | uspto-grants-2016_04 |
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