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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596232Generated: November 4, 2026

Pyridine → HCID 21701663, compound

https://huagongshe.com/reaction/1596232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactanttert-Butyl piperazin-1-ylcarbamateHCID 21701658—
SolventDichloromethaneHCID 6344—
ProductHCID 21701663HCID 21701663—

Reaction Steps

To a solution of N-(1-piperazinyl)-tert-butoxycarboxamide (15 g) in dichloromethane (200 ml) was added acetic anhydride (7.74 ml) and pyridine (6.63 ml). The mixture was stirred at ambient temperature for 1 hour. The solution was washed with saturated aqueous solution of sodium hydrogen carbonate and brine. The organic layer was collected, dried over magnesium sulfate, and concentrated. The residue was triturated with n-hexane to give N-(4-acetyl-1-piperazinyl)-tert-butoxycarboxamide (16.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291464B1
Source datasetuspto-grants-2001_09
ORD IDord-7bfd8d3e7cd641c5bbe22ae679bd922f
Source noteuspto-grants-2001_09