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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 864774Generated: November 1, 2026

1-(4-Pyridyl)piperazine → HCID 18918480, compound

https://huagongshe.com/reaction/864774

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Pyridyl)piperazineHCID 70517—
ReactantHCID 18918612HCID 18918612—
SolventAcetonitrileHCID 6342—
ProductHCID 18918480HCID 18918480—

Reaction Steps

A solution of N-([4-bromoacetylphenyl]methyl)-4-methylphenylsulphonamide (470 mg) in acetonitrile (10 ml) was added to a stirred solution of 1-(4-pyridyl)piperazine (400 mg) in acetonitrile (10 ml) and the mixture stirred for 18 hours. The solvent was evaporated in vacuo and the residue purified by flash chromatography on silica, eluting with 10% v/v methanol/dichloromethane. On evaporation of the eluant fraction to a small volume crystallisation occurred. These crystals, on filtration and washing with dichloromethane gave the title compound, 130 mg, as a solid: m.p. 215°-219° C. dec.; NMR(d6DMSO) δ8.14(3H,m), 7.91(2H,d), 7.69(2H,d), 7.38(4H,d), 6.82(2H,d), 4.03(2H,d), 3.89(2H,s), 3.32(4H,t), 2.62(4H,t), 2.39(3H,s); m/e 465(M+H)+ ; calculated for C25H28N4O3S: C, 64.6; N, 6.1; N, 12.1. found C, 64.7; H, 6.2; N, 12.0%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05563141
Source datasetuspto-grants-1996_10
ORD IDord-ddd89a75cd6447f3ba101bd9c987cf7e
Source noteuspto-grants-1996_10