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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278879Generated: November 2, 2026

Ammonium Chloride → 5-Amino4-(3-aminobenzoyl)-1-(4-fluorophenyl)pyrazole

https://huagongshe.com/reaction/1278879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Amino-1-(4-fluorophenyl)-4-(3-nitrobenzoyl)pyrazoleHCID 22262759—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product5-Amino4-(3-aminobenzoyl)-1-(4-fluorophenyl)pyrazoleHCID 2226281096.4%

Reaction Steps

A mixture of 5-amino-1-(4-fluorophenyl)-4-(3-nitrobenzoyl)pyrazole (4.0 g, 24.52), Fe powder (3.84 g, 68 mmol) and ammonium chloride (3.84, 71.78 mmol) in ethanol (135 ml) and water (64 ml) was heated at reflux under nitrogen atmosphere. After 1 h, the reaction mixture was cooled to room temperature and stirred overnight. The reaction mixture was filtered through Celite® and the filtrate was concentrated in vacuo. The residue was partitioned between water and ethyl acetate. The organic layer was separated and washed with brine, dried over sodium sulfate and concentrated in vacuo to give 5-amino-4-(3-aminobenzoyl)-1-(4-fluorophenyl)pyrazole (3.5 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444696B1
Source datasetuspto-grants-2002_09
ORD IDord-e93b07df772a41de9f346d82637b37b6
Source noteuspto-grants-2002_09