HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890277Generated: November 1, 2026
6-(Benzyloxy)-3-nitropyridin-2-amine → 6-(Benzyloxy)pyridine-2,3-diamine
https://huagongshe.com/reaction/1890277
Participants
| Role | Name | HCID | Charge |
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| Reactant | 6-(Benzyloxy)-3-nitropyridin-2-amine | HCID 10800379 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 6-(Benzyloxy)pyridine-2,3-diamine | HCID 67311804 | 97% |
Reaction Steps
To a solution of 6-(benzyloxy)-3-nitropyridin-2-amine (J. Med. Chem. 1997, 40, 1808) (22.67 g, 92.44 mmol) in AcOH (300 mL) was added zinc dust (24.18 g, 369.7 mmol) in four portions over 10 min while cooling in an ice bath. The mixture was then allowed to warm to room temperature and stirred for 2 h. The mixture was filtered and the solvent was removed under reduced pressure. The product was taken up in EtOAc and washed with saturated NaHCO3 solution and brine. The organics were dried over MgSO4, filtered and concentrated to yield the title compound as a black solid (19.31 g). 1H NMR (400 MHz, DMSO-d6) δ ppm 4.13 (s, 2H), 5.14 (s, 2H), 5.39 (s, 2H), 5.86 (d, J=7.9 Hz, 1H), 6.77 (d, J=7.9 Hz, 1H), 7.28 (m, 1H), 7.34 (t, J=7.6 Hz, 2H), 7.40 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08507473B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-51573f2995ac48c9894a1ca514798d75 |
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| Source note | uspto-grants-2013_08 |
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