HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 626772Generated: October 30, 2026
4-Bromo-2-(2,6-dichloro-4-nitrophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine → 2-(4-Bromo-7-fluoropyrazolo[4,3-c]pyridin-2-yl)-3-chloro-5-nitrobenzonitrile
https://huagongshe.com/reaction/626772
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Bromo-2-(2,6-dichloro-4-nitrophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine | HCID 86697069 | — |
| Reactant | 3-Chloro-2-(4-chloro-7-fluoropyrazolo[4,3-c]pyridin-2-yl)-5-nitrobenzonitrile | HCID 86697071 | — |
| Product | 2-(4-Bromo-7-fluoropyrazolo[4,3-c]pyridin-2-yl)-3-chloro-5-nitrobenzonitrile | HCID 86697070 | 83% |
Reaction Steps
Following the procedure described for 4-bromo-2-(2,6-dichloro-4-nitrophenyl)-7-fluoro-2H-pyrazolo[4,3-c]pyridine, 3-chloro-2-(4-chloro-7-fluoropyrazolo[4,3-c]pyridin-2-yl)-5-nitrobenzonitrile was heated at 100° C. overnight to afford the title compound as a pale yellow solid (1.38 g, 83% yield). LCMS (Method C): RT=3.62 min, m/z: 396 [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-529384bd491f4688a20840bad1179880 |
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| Source note | uspto-grants-2016_04 |
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