HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353356Generated: October 30, 2026
8-Azido-5,6,7,8-tetrahydroquinoline → 8-Amino-5,6,7,8-tetrahydroquinoline
https://huagongshe.com/reaction/353356
Participants
| Role | Name | HCID | Charge |
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| Reactant | 8-Azido-5,6,7,8-tetrahydroquinoline | HCID 22708769 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 8-Amino-5,6,7,8-tetrahydroquinoline | HCID 11355564 | 71% |
Reaction Steps
To a solution of the azide (41.0 g, 0.256 mol) in methanol (250 mL) was added Pd/C (10%, 4.1 g) and the mixture was hydrogenated at 30 psi on a Parr shaker. The mixture was filtered through celite and the cake was washed with methanol. The combined filtrates were evaporated and the residual oil was distilled (Kugelrohr, bp 115-140° C. @ 0.2 Torr) to provide 26.8 g (71%) of 8-amino-5,6,7,8-tetrahydroquinoline (AMD7488) as a pale yellow oil. 1H NMR (MeOH-d4) δ 1.81-1.98 (m, 2H), 2.03-2.15 (m, 1H), 2.38-2.46 (m, 1H), 2.88-2.92 (m, 2H), 4.41 (dd, 1H, J=9.3, 6.3 Hz), 7.30 (dd, 1H, J=7.5, 4.5 Hz), 7.62 (d, 1H, J=7.5 Hz), 8.47 (d, 1H, J=4.5 Hz); 13C NMR (MeOH-d4) δ 21.12, 28.72, 28.89, 52.28, 124.86, 134.35, 138.96, 148.49, 152.57. ES-MS m/z 149 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06750348B1 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-38bfd53c89bc4b6c9c18981a94d67363 |
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| Source note | uspto-grants-2004_06 |
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