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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540758Generated: October 29, 2026

3-[1-ethyl-5-(4-fluoro-2-nitrophenoxy)-1H-pyrazol-3-yl]benzonitrile → 3-[5-(2-amino-4-fluorophenoxy)-1-ethyl-1H-pyrazol-3-yl]benzonitrile

https://huagongshe.com/reaction/540758

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[1-ethyl-5-(4-fluoro-2-nitrophenoxy)-1H-pyrazol-3-yl]benzonitrileHCID 67111584—
ReactantHCID 178418361HCID 178418361—
SolventMethanolHCID 887—
Product3-[5-(2-amino-4-fluorophenoxy)-1-ethyl-1H-pyrazol-3-yl]benzonitrileHCID 67111064—

Reaction Conditions

Temperature22 °C

Reaction Steps

Pt/Vd (3%/0.6% wt/wt on carbon, 50 mg, 0.008 mmol, 0.005 equiv) was added to a stirring solution of 3-[1-ethyl-5-(4-fluoro-2-nitrophenoxy)-1H-pyrazol-3-yl]benzonitrile (0.54 g, 1.53 mmol, 1 equiv) in methanol (15.3 mL). A 3-way stop cock with a hydrogen balloon was installed and the reaction vessel was subjected to alternating vacuum and H2 gas (4×). The resulting mixture was stirred at 22° C. for 2 hours. The mixture was then subjected to alternating vacuum and nitrogen gas (4×) before the mixture was filtered through a nylon syringe filter and concentrated in vacuo to afford 3-[5-(2-amino-4-fluorophenoxy)-1-ethyl-1H-pyrazol-3-yl]benzonitrile. The crude reaction product was carried forward without further purification. Calcd (M+1)+: 323.1. Found: 323.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871796B2
Source datasetuspto-grants-2014_10
ORD IDord-19af053e481742f9a328d929e7a5b17a
Source noteuspto-grants-2014_10