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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290471Generated: November 3, 2026

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

https://huagongshe.com/reaction/1290471

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) δ 8.14(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 numberUS05750754
Source datasetuspto-grants-1998_05
ORD IDord-fe3a69a490214503b86ab46c1287dce7
Source noteuspto-grants-1998_05