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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1825434Generated: November 2, 2026

Ethylenediamine → Tert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate

https://huagongshe.com/reaction/1825434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantTert-butyl 6-chloropyridine-3-carboxylateHCID 11521348—
ProductTert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylateHCID 22142445—

Reaction Steps

The tert-butyl 6-chloropyridine-3-carboxylate was heated with ethylenediamine (20 ml) at 80° C. overnight. The solvent was removed in vacuo. The residue was partitioned between dichloromethane and 2.5 M aqueous sodium hydroxide solution. The aqueous layer was extracted a further three times with dichloromethane. The combined organic layers were washed with water, dried and concentrated in vacuo to give tert-butyl 6-[(2-aminoethyl)amino]pyridine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07045519B2
Source datasetuspto-grants-2006_05
ORD IDord-8705ee0f02a6423092fd41815e972578
Source noteuspto-grants-2006_05