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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 843055Generated: October 25, 2026

(4-Fluorophenyl)hydrazine → 5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole

https://huagongshe.com/reaction/843055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Fluorophenyl)hydrazineHCID 69982—
Reactant2-(3-Bromobenzoyl)-3-phenylaminoacrylonitrileHCID 69686607—
SolventEthanolHCID 702—
SolventHexaneHCID 8058—
Product5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazoleHCID 1145123787.7%

Reaction Steps

A mixture of 4-fluorophenylhydrazine (4.25 g, 33.7 mmol) and 2-(3-bromobenzoyl)-3-phenylaminoacrylonitrile (10.0 g, 30.7 mmol) in ethanol (100 ml) was heated at reflux under a nitrogen atmosphere. After 4 h, the reaction mixture was cooled to room temperature, diluted with hexane to give 5-amino-4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole (9.7 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06376527B1
Source datasetuspto-grants-2002_04
ORD IDord-10c493b9e8b14faea8efb92fc990d6a5
Source noteuspto-grants-2002_04