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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531458Generated: November 4, 2026

Piperazine → Diethyl-4-piperazinyl-2,6-pyridinedicarboxylate

https://huagongshe.com/reaction/1531458

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantDiethyl 4-bromopyridine-2,6-dicarboxylateHCID 13794409—
Solvent1,4-DioxaneHCID 31275—
ProductAmmonium HydroxideHCID 1492330%
ProductDiethyl-4-piperazinyl-2,6-pyridinedicarboxylateHCID 85702736198.5%

Reaction Steps

A mixture of diethyl 4-bromopyridine-2,6-dicarboxylate (Example 49) (3.02 g, 10.0 mmol) and piperazine (Aldrich, 4.3 g, 50 mmol) in dioxane (200 mL) was refluxed for 24 hours. The precipitate was filtered off and the filtrate was concentrated under vacuum. The residue was dissolved in ethyl acetate and washed four times with brine. The organic solution was dried (Na2SO4) and the solvent was evaporated. The residue was purified by flash chromatography on a silica gel column (22 cm×3 cm). Elution with methanol and then methanol:30% ammonium hydroxide (100:1, 50:1, and 20:1, v/v) gave 3.05 g (99%) of the title compound as a pale yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06197965B1
Source datasetuspto-grants-2001_03
ORD IDord-4c129075f6094680b9c21fdc99594b50
Source noteuspto-grants-2001_03