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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11558Generated: October 25, 2026

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

https://huagongshe.com/reaction/11558

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 numberUS07098236B2
Source datasetuspto-grants-2006_08
ORD IDord-eb1ff254344f4230a9d813e4b5254294
Source noteuspto-grants-2006_08