HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266740Generated: October 26, 2026
1-(4-Pyridyl)piperazine → Ethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetate
https://huagongshe.com/reaction/266740
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Reactant | Ethyl 2-[4-(2-bromoacetyl)phenoxy]acetate | HCID 18408936 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Ethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxyacetate | HCID 18918266 | — |
Reaction Steps
Ethyl 4-bromoacetylphenoxyacetate (6.0 g) was added to a stirred, cooled (4° C.) solution of 1-(4-pyridyl)piperazine (6.5 g) in acetonitrile (225 ml). Stirring was continued for 1 hour at 4° C., then overnight at ambient temperature when the precipitated solid was removed by filtration. The filtrate was evaporated in vacuo and the solid residue triturated with water, filtered, then washed with water and dried. Recrystallisation from a small volume of ethanol gave the title compound, 1.71 g, as a cream coloured solid: m.p. 113°-114° C.; (d6DMSO) δ 8.15 (2H, d), 7.98 (2H, d), 7.02 (2H, d), 6.80 (2H, d), 4.89 (2H, d), 4.17 (2H, q), 3.84 (2H, s), 3.32 (4H, t), 2.62 (4H, t), 1.22 (3H, t); m/e 384 (M+H)+ ; calculated for C21H25N3O4 : C, 65.8; H, 6.6; N, 11.0. found: C, 65.5; H, 6.6; N, 10.8%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05652242 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-2be04a7ca45447cfba0de30476c8ee08 |
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| Source note | uspto-grants-1997_07 |
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