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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1829190Generated: November 2, 2026

Triethylamine → tert-Butyl4-(3-cyano-2-pyridinyl)-1-piperazinecarboxylate

https://huagongshe.com/reaction/1829190

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-ChloronicotinonitrileHCID 81079—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
SolventTolueneHCID 1140—
Producttert-Butyl4-(3-cyano-2-pyridinyl)-1-piperazinecarboxylateHCID 22061422—

Reaction Steps

A mixture of 2-chloro-3-cyanopyridine (15.2 g, 0.11 mol), tert-butyl 1-piperazinecarboxylate (25 g, 0.13 mol) and triethylamine (18 ml, 0.13 mol) in toluene (200 ml), was heated under reflux for 24 hours. The cooled mixture was concentrated under reduced pressure and the residue suspended in ethyl acetate (250 ml), and washed with water (3×). The organic solution was dried (MgSO4), and concentrated under reduced pressure. The residue was triturated with pentane, filtered and dried in vacuo, at 60° C., to afford the title compound as a cream coloured solid, 24.2 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07060836B2
Source datasetuspto-grants-2006_06
ORD IDord-4170c0f4d1d74f3ab1306d06b36dbb36
Source noteuspto-grants-2006_06