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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352225Generated: October 25, 2026

1-Acetylpiperazine → (4-Acetyl-piperazin-1-yl)pyridin-3-yl-acetic acid ethyl ester

https://huagongshe.com/reaction/352225

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantEthyl 2-bromo-2-(pyridin-3-yl)acetateHCID 21985933—
Product(4-Acetyl-piperazin-1-yl)pyridin-3-yl-acetic acid ethyl esterHCID 6984940760%

Reaction Steps

N-acetyl-piperazine (3.7 g; 28.8 mmol; 2.8 equiv) was combined with bromo-pyridin-3-yl-acetic acid ethyl ester (approx. 2.5 g; 10 mmol). Purification on a 3×16 cm silica column using a 30% then 40% ethyl acetate/hexanes (v/v) mobile phase followed by a 2% methanol/dichloromethane (v/v) mobile phase resulted in 1.84 g light yellow oil (approx. 60% yield). MS(ES) calc'd: [M+H]+=292.2 m/z; [M+Na]+=314.2 m/z.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743794B2
Source datasetuspto-grants-2004_06
ORD IDord-5f7765389b5b496bb3641e9d3af6995f
Source noteuspto-grants-2004_06