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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899667Generated: October 26, 2026

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

https://huagongshe.com/reaction/899667

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 numberUS07354932B2
Source datasetuspto-grants-2008_04
ORD IDord-a6707fd1b8f94633bdfbce784ea4e442
Source noteuspto-grants-2008_04