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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 79478Generated: October 29, 2026

1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole → 3-ethyl-1-((5-fluoropyridin-2-yl)methyl)-1H-indazol-4-amine

https://huagongshe.com/reaction/79478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazoleHCID 67259856—
CatalystPalladium hydroxideHCID 9942167—
SolventEthanolHCID 702—
Product3-ethyl-1-((5-fluoropyridin-2-yl)methyl)-1H-indazol-4-amineHCID 6726014590.6%

Reaction Steps

A solution of 1-((5-fluoropyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole (0.229 g, 0.768 mmol) in EtOH (4 mL) was purged with argon. To this solution was added palladium hydroxide on carbon (91 mg, 40%/wt). The mixture was purged with more argon and then hydrogen. The mixture was then stirred at ambient temperature under hydrogen for 16 hours. The mixture was filtered through GF/F paper, washed with MeOH and concentrated under reduced pressure to give 3-ethyl-1-((5-fluoropyridin-2-yl)methyl)-1H-indazol-4-amine (188 mg) as an amber oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08841455B2
Source datasetuspto-grants-2014_09
ORD IDord-14548ac1e778422ea8f7eaecf3bf5d43
Source noteuspto-grants-2014_09