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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278878Generated: November 3, 2026

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

https://huagongshe.com/reaction/1278878

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Fluorophenyl)hydrazineHCID 69982—
Reactant2-(3-Nitrobenzoyl)-3-phenylaminoacrylonitrileHCID 69686076—
SolventEthanolHCID 702—
Product5-Amino-1-(4-fluorophenyl)-4-(3-nitrobenzoyl)pyrazoleHCID 2226275997.4%

Reaction Steps

A mixture of 4-fluorophenylhydrazine (2.24 g, 15.57 mmol) and 2-(3-nitrobenzoyl)-3-phenylaminoacrylonitrile (4.15 g, 14.16 mmol) in ethanol (50 ml) was heated at reflux under nitrogen atmosphere. After 1 h, the reaction mixture was cooled to room temperature and stirred for an additional 3 h. The solid was filtered and dried to give 5-amino-1-(4-fluorophenyl)-4-(3-nitrobenzoyl)pyrazole (4.5 g) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444696B1
Source datasetuspto-grants-2002_09
ORD IDord-04fe1ed4932d475980fd55fa30d94ca9
Source noteuspto-grants-2002_09