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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489855Generated: October 26, 2026

(4-Fluorophenyl)hydrazine → 5-Amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole

https://huagongshe.com/reaction/489855

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Fluorophenyl)hydrazineHCID 69982—
Reactant2-(3-Iodobenzoyl)-3-phenylaminoacrylonitrileHCID 67024274—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
Product5-Amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazoleHCID 986607587.4%

Reaction Steps

A mixture of 4-fluorophenylhydrazine (26.6 g, 211 mmol) and 2-(3-iodobenzoyl)-3-phenylaminoacrylonitrile (79 g, 211 mmol) in ethanol (400 ml) was heated at reflux under a nitrogen atmosphere. After 30 minutes, the reaction mixture was cooled to room temperature, diluted with hexane to give 5-amino-4-(3-iodobenzoyl)-1-(4-fluorophenyl)pyrazole (75.1 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979693B2
Source datasetuspto-grants-2005_12
ORD IDord-af22b01406424d148aec0dcc8ee3e85a
Source noteuspto-grants-2005_12