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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744382Generated: November 1, 2026

Hydrazine hydrate (1:1) → N~1~-[3-(4-Methylpiperazin-1-yl)propyl]benzene-1,4-diamine

https://huagongshe.com/reaction/1744382

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
ReactantN-[3-(4-methylpiperazin-1-yl)propyl]-4-nitro-1-aminobenzeneHCID 21975010—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductN~1~-[3-(4-Methylpiperazin-1-yl)propyl]benzene-1,4-diamineHCID 21975027—

Reaction Conditions

Temperature50 °C

Reaction Steps

A suspension of 0.1385 gms. of [3-(4-methyl-piperazin-1-yl)-propyl]-(4-nitro-phenyl)-amine in 3 mL of ethanol is heated to 50° C. Once dissolution is achieved 0.144 mL hydrazine monohydrate is addded to the solution. A Raney nickel slurry in water is added to the 50° C. solution dropwise, waiting after each addition for the gas evolution to cease. Sufficient quantities of Raney nickel have been added when continued addition of Raney nickel causes no further gas evolution. The reaction is then maintained at 50° C. for an additional hour, and subsequently is cooled to room temperature. The reaction mixture is filtered through a pad of celite (rinsing the pad with methanol). N-[3-(4-Methyl-piperazin-1-yl)-propyl]-benzene-1,4-diamine (0.116 gms.) is isolated upon evaporation of the filtrate, and is subsequently used without purification in the reaction of Example 302.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015220B2
Source datasetuspto-grants-2006_03
ORD IDord-1162d980e7b64ae9b090aa65da794a69
Source noteuspto-grants-2006_03