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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429373Generated: October 30, 2026

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

https://huagongshe.com/reaction/429373

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 numberUS06316466B1
Source datasetuspto-grants-2001_11
ORD IDord-c1e58d3e393f49aa90e853419f9eba29
Source noteuspto-grants-2001_11