Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydrideHCID 82127—
ReactantMethyl 4-bromoacetylphenoxyacetateHCID 243438—
Reactant4-(Pyridin-4-YL)piperazin-2-oneHCID 18918356—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-[2-[4-(4-pyridyl)piperazin-2-one-1-yl]acetyl]phenoxyacetateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750754
Source datasetuspto-grants-1998_05
ORD IDord-34b62b3defd64b40ab61bffb4a64cd9e
Source noteuspto-grants-1998_05