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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(Benzyloxy)-3-nitropyridin-2-amineHCID 10800379—
CatalystZincHCID 23994—
SolventAcetic AcidHCID 176—
Product6-(Benzyloxy)pyridine-2,3-diamineHCID 6731180497%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507473B2
Source datasetuspto-grants-2013_08
ORD IDord-51573f2995ac48c9894a1ca514798d75
Source noteuspto-grants-2013_08