HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79477Generated: October 28, 2026
Potassium vinyltrifluoroborate → 1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole
https://huagongshe.com/reaction/79477
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Reactant | HCID 67261198 | HCID 67261198 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Tetrahydrofuran 2-propanol | HCID 22597222 | — |
| Product | 1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole | HCID 67259856 | — |
Reaction Steps
A suspension of 1-((5-fluoropyridin-2-yl)methyl)-3-iodo-4-nitro-1H-indazole (0.968 g, 2.43 mmol) in 4:1 IPA/THF (10 mL) was degassed under argon. To the suspension was added TEA (0.678 mL, 4.86 mmol), potassium trifluoro(vinyl)borate (0.651 g, 4.86 mmol) and PdCl2(dppf)*dcm (0.199 g, 0.243 mmol). The mixture was then heated with stirring at 90° C. for 16 hours under argon. The mixture was allowed to cool, filtered through GF/F paper and concentrated under reduced pressure. The residue was dissolved in DCM and purified by chromatography on silica using a Biotage system, eluting with 1-10% Et2O in DCM. This gave 1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole (229 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08841455B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-db8c01992de046a6bc3560eaf1848133 |
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| Source note | uspto-grants-2014_09 |
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