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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1725146Generated: November 2, 2026

1-(3-fluorobenzyl)-5-nitro-1H-indazole → 1-(3-Fluorobenzyl)-1H-indazol-5-amine

https://huagongshe.com/reaction/1725146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(3-fluorobenzyl)-5-nitro-1H-indazoleHCID 21966490—
CatalystPlatinumHCID 23939—
SolventEthanolHCID 702—
Product1-(3-Fluorobenzyl)-1H-indazol-5-amineHCID 7147073—

Reaction Conditions

Temperature60 °C

Reaction Steps

Follow modified procedure from WO 99/35146. 1-(3-Fluoro-benzyl)-5-nitro-1H-indazole (2.49 g, 9.2 mmol) is suspended in 40 ml absolute EtOH and Pt/C (5%, wet, 150 mg) is added. The reaction mixture is stirred and heated at 60° C. under a hydrogen atmosphere (balloon). Roughly 4 hours into the reaction LC/MS reveals the formation of substantial amounts of product. The mixture is filtered through Celite and concentrated under reduced pressure. Yield: 2.01 g (90.8%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07488823B2
Source datasetuspto-grants-2009_02
ORD IDord-b37e29c35d934096b4c6e57a2ceba2eb
Source noteuspto-grants-2009_02