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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1610086Generated: October 30, 2026

3-(3-fluorophenyl)-6-nitro-1H-indazole → 3-(3-Fluorophenyl)-1H-6-indazolamine

https://huagongshe.com/reaction/1610086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(3-fluorophenyl)-6-nitro-1H-indazoleHCID 22260895—
CatalystHCID 178502593HCID 178502593—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
Product3-(3-Fluorophenyl)-1H-6-indazolamineHCID 2226068853.6%

Reaction Steps

To a solution of 300 mg of 3-(3-fluorophenyl)-6-nitro-1H-indazole in 5 ml methanol and 2.5 ml ethyl acetate was added 60 mg of 20% palladium hydroxide-carbon (water content: 50%), and the mixture was subjected to hydrogenation at room temperature at normal pressure for 7.5 hours. After adding 2.5 ml of ethyl acetate to the reaction mixture, the catalyst was filtered off through Celite. The solvent was evaporated, and the crude product was suspended in ethyl acetate-diisopropyl ether, to give 142 mg of the title compound as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06982274B2
Source datasetuspto-grants-2006_01
ORD IDord-bd3e0ba39c434c3d9f7772da4b7e27fc
Source noteuspto-grants-2006_01