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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266725Generated: October 26, 2026

1-(4-Pyridyl)piperazine → Methyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]-2-methylacetyl]phenoxyacetate

https://huagongshe.com/reaction/266725

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-Pyridyl)piperazineHCID 70517—
ReactantMethyl (4-propanoylphenoxy)acetateHCID 16762866—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-[2-[4-(4-pyridyl)piperazin-1-yl]-2-methylacetyl]phenoxyacetateHCID 18918574—

Reaction Steps

A solution of RS methyl 4-(2-methylacetyl)phenoxyacetate (1.2 g) in acetonitrile (10 ml) was added dropwise over 30 minutes to a stirred solution of 1-(4-pyridyl)piperazine (1.3 g) in acetonitrile (30 ml) and the mixture stirred overnight. The mixture was then filtered and the filtrate evaporated to give an oil. Purification by flash chromatography, eluting first with dichloromethane then successively 2.5%, 3%, 4%, 5% and 10% v/v methanol/dichloromethane gave the title compound, 220 mg as a solid: m.p. 81°-83° C.; NMR (d6DMSO) δ 8.13(2H,d), 8.06(2H,d), 7.02(2H,d), 6.77(2H,d), 4.92(2H,s), 4.33(1H,q), 3.72(3H,s), 3.26(4H,t), 2.63(4H,t), 1.16(3H,d); m/e 384(M+H)+ ; calculated for C21H25N3O4 : C, 65.8; H, 6.6; N, 11.0. found C, 65.7; H, 6.8; N, 10.9%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652242
Source datasetuspto-grants-1997_07
ORD IDord-34624abe82cf42718e3dc3e88a2092de
Source noteuspto-grants-1997_07