Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236530Generated: October 31, 2026

Acetic Acid → tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2236530

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 11243758—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
Producttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 1173752578%

Reaction Conditions

Temperature60 °C

Reaction Steps

An amount of 2 g (6.48 mmol) of, tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate, 1.4 g (25.9 mmol) of iron, and acetic acid (3.1 mL, 48.6 mmol) were placed in a flask. Methanol (30 mL) is added and heat at 60° C. for 2 hours. After cooling to room temperature, the precipitate is filtered, the methanol is removed in a vacuum and saturated sodium bicarbonate is added. The mixture is extracted 3× with ethyl acetate. Dried over sodium sulfate, and evaporated to give 1.43 g (78% yield) as a purple solid. MS (ESI) m/z 279.1(M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07713994B2
Source datasetuspto-grants-2010_05
ORD IDord-a577fbe06cf34ffe9f29ac8e6e683495
Source noteuspto-grants-2010_05