HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290490Generated: October 26, 2026
Potassium hydride → Methyl 4-[2-[4-(4-pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetate
https://huagongshe.com/reaction/1290490
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium hydride | HCID 82127 | — |
| Reactant | Methyl 4-bromoacetylphenoxyacetate | HCID 243438 | — |
| Reactant | 4-(Pyridin-4-YL)piperazin-2-one | HCID 18918356 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-[2-[4-(4-pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetate | HCID 18918332 | — |
Reaction Steps
A dispersion of potassium hydride in mineral oil (35% w/w, 0.63 g) was added to a stirred suspension of 4-(4-pyridyl)piperazin-2-one (0.885 g) in DMF (10 ml) and the mixture was stirr-ed at room temperature for 2 hours. To the anion thus formed, was added methyl 4-bromoacetylphenoxyacetate (1.44 g) and the mixture was stirred at room temperature for 20 hours. Solvent was evaporated and the residue partitioned between dichloromethane (20 ml) and water (20 ml). The organic layer was dried (MgSO4) and evaporated. The residue was purified by flash column chromatography, the product being eluted with 1/9/0.1 v:v:v methanol/dichloromethane/0.88 S.G aqueous ammonia. Recrystallisation from ethyl acetate gave the title compound, m.p. 164°-165° C.; NMR (d6DMSO) δ 8.2(2H,d), 7.97(2H,d), 7.08(2H,d), 6.83(2H,d), 4.93(4H,d), 4.02(2H,s), 3.71(3H,s), 3.7(2H,m), 3.52(2H,m); m/e 384 (M+H)+ ; calculated for C20H21N3O5 : C, 62.7; H, 5.52; N, 11.0. Found: C, 62.6; H, 5.6; N, 10.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05750754 |
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| Source dataset | uspto-grants-1998_05 |
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| ORD ID | ord-34b62b3defd64b40ab61bffb4a64cd9e |
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| Source note | uspto-grants-1998_05 |
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