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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624312Generated: October 31, 2026

5-Azido-5,6,7,8-tetrahydroquinoxaline → 5,6,7,8-Tetrahydroquinoxalin-5-amine

https://huagongshe.com/reaction/1624312

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Azido-5,6,7,8-tetrahydroquinoxalineHCID 58149493—
CatalystPalladiumHCID 23938—
Product5,6,7,8-Tetrahydroquinoxalin-5-amineHCID 1209906399.9%

Reaction Steps

A Parr shaker flask was charged with 5-azido-5,6,7,8-tetrahydroquinoxaline (1.81 g, 10.33 mmol) and 10% palladium on carbon (10 wt % of Pd/C, 0.18 g). The reaction vessel was evacuated and filled with nitrogen. Methanol (30 mL) was added and the reaction was hydrogenated at 30 psi for 40 minutes. The reaction mixture was flushed with nitrogen and filtered through a plug of Celite® to provide 5,6,7,8-tetrahydroquinoxalin-5-ylamine as an orange liquid (1.54 g, 99%), which would rapidly turn dark brown. It was stored under an argon atmosphere at −20° C. 1H NMR (CDCl3): δ 1.62-1.79 (m, 1H), 1.80-2.18 (m, 4H), 2.18-2.30 (m, 1H), 2.91-3.01 (m, 2H), 4.07 (dd, 1H, J=8.4, 5.4 Hz), 8.32-8.38 (m, 2H); 13C NMR (CDCl3): δ 19.7, 31.7, 32.2, 51.5, 142.0, 142.5, 152.6, 155.4; MS m/z: 150 (M+H+), 133.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778967B2
Source datasetuspto-grants-2014_07
ORD IDord-e86545b4cf14491e81ef14cd01a81f62
Source noteuspto-grants-2014_07