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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241934Generated: October 31, 2026

Water → N4-cyclohexylmethyl-2-(4-methyl-piperazin-1-yl)-5-nitro-N1-phenyl-benzene-1,4-diamine

https://huagongshe.com/reaction/1241934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantN4-cyclohexylmethyl-2-fluoro-5-nitro-N1-phenyl-benzene-1,4-diamineHCID 21061670—
SolventDimethylformamideHCID 6228—
ProductN4-cyclohexylmethyl-2-(4-methyl-piperazin-1-yl)-5-nitro-N1-phenyl-benzene-1,4-diamineHCID 2106166980.7%

Reaction Steps

A solution of N4-cyclohexylmethyl-2-fluoro-5-nitro-N1-phenyl-benzene-1,4-diamine (0.23 g, 0.66 mmol), N-methylpiperazine (0.22 mL, 1.97 mmol) and N,N′-diisopropylethylamine (0.34, 1.97 mmol) in DMF (3.0 mL) was stirred at 100° C. under an inert atmosphere for 16 h. The reaction mixture was transferred to a separatory funnel containing water. The aqueous layer was extracted with EtOAc and the combined organic layers were washed with water, brine and dried over MgSO4. The solution was filtered through diatomaceous earth and the solvent was evaporated. The resulting dark red residue was flash chromatographed (5% MeOH/CH2Cl2) to give N4-cyclohexylmethyl-2-(4-methyl-piperazin-1-yl)-5-nitro-N1-phenyl-benzene-1,4-diamine as a red foam (0.22 g, 80.7% yield). M+, 424

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115644B2
Source datasetuspto-grants-2006_10
ORD IDord-01af52ea6a9b4085a881b35077b3bda5
Source noteuspto-grants-2006_10