Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915704Generated: November 2, 2026

2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamine → 3-Fluoro-4-(4-methylpiperazin-1-yl)benzene-1,2-diamine

https://huagongshe.com/reaction/1915704

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoro-3-(4-methyl-piperazin-1-yl)-6-nitro-phenylamineHCID 22040816—
CatalystLindlars catalystHCID 131709914—
SolventMethanolHCID 887—
Product3-Fluoro-4-(4-methylpiperazin-1-yl)benzene-1,2-diamineHCID 22040743—

Reaction Steps

A reaction tube was charged with suspension of 1 (330 mg, 1.15 mmol) and Lindlar catalyst (245 mg, 10 mol %) in methanol (5 mL), sealed, and placed on a Parr shaker. The reaction was pressurized with H2 (60 psi) and maintained for 1 h. The reaction was filtered through Celite and the remaining solids were washed with MeOH. The combined organics were concentrated to give 2 as a brown semi-solid which was taken on without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614330B2
Source datasetuspto-grants-2013_12
ORD IDord-895ddd6c66b54bdd958dc7bb33f5e26b
Source noteuspto-grants-2013_12