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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16413Generated: October 27, 2026

1h-Indazole,4-(2-fluoro-4-nitrophenoxy)- → 3-Fluoro-4-(1H-indazol-4-yloxy)aniline

https://huagongshe.com/reaction/16413

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1h-Indazole,4-(2-fluoro-4-nitrophenoxy)-HCID 17979311—
CatalystAdams' catalystHCID 345198—
SolventTetrahydrofuran ethanolHCID 21873804—
Product3-Fluoro-4-(1H-indazol-4-yloxy)anilineHCID 17979339—

Reaction Steps

Under argon, 60 mg (0.22 mmol) of 4-(2-fluoro-4-nitrophenoxy)-1H-indazole (from example XXV) are initially charged in 5 ml of ethanol/tetrahydrofuran (1:1), 9.97 mg (0.04 mmol) of platinum(IV) oxide are added and the mixture is hydrogenated under atmospheric pressure for 2 hours. The suspension is filtered off through CELITE (diatomaceous earth), the filtercake is washed with ethanol and the filtrate is concentrated under reduced pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737153B2
Source datasetuspto-grants-2010_06
ORD IDord-d48c9432d27d412c9e71f902df366c04
Source noteuspto-grants-2010_06