HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1291810Generated: October 30, 2026
1-(4-Pyridyl)piperazine → HCID 18918480, compound
https://huagongshe.com/reaction/1291810
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Reactant | HCID 18918612 | HCID 18918612 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18918480 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05753659 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-431ef240799b462eb33519aa5feebbfd |
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| Source note | uspto-grants-1998_05 |
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