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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium vinyltrifluoroborateHCID 23679353—
ReactantHCID 67261198HCID 67261198—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventTetrahydrofuran 2-propanolHCID 22597222—
Product1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazoleHCID 67259856—

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-db8c01992de046a6bc3560eaf1848133
Source noteuspto-grants-2014_09