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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489848Generated: October 30, 2026

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

https://huagongshe.com/reaction/489848

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 numberUS06979693B2
Source datasetuspto-grants-2005_12
ORD IDord-e4ca3b4e62f9430e9bffe7cf805682e6
Source noteuspto-grants-2005_12