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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916478Generated: October 31, 2026

5'-Fluoro-5-nitro-3,3'-bipyridin-4-amine → 5'-Fluoro-3,3'-bipyridine-4,5-diamine

https://huagongshe.com/reaction/1916478

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5'-Fluoro-5-nitro-3,3'-bipyridin-4-amineHCID 86701065—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5'-Fluoro-3,3'-bipyridine-4,5-diamineHCID 86701066100%

Reaction Steps

To a solution of 5′-fluoro-5-nitro-3,3′-bipyridin-4-amine (LXXI) (621 mg, 2.65 mmol) in EtOH (18 mL) was added 10% Pd/C (93 mg, 15% by wt). The solution was purged with hydrogen and stirred for overnight at room temperature under hydrogen. The suspension was filtered through Celite and concentrated under vacuum. The crude product was purified through a silica gel column (100% CHCl3→3:97MeOH[7N NH3]:CHCl3) to produce 5′-fluoro-3,3′-bipyridine-4,5-diamine (LXII) as an off-white solid (542 mg, 2.65 mmol, 100% yield). 1H NMR (DMSO-d6, 500 MHz) δ ppm 4.78 (brs, 2H), 5.28 (brs, 2H), 7.46 (s, 1H), 7.70 (s, 1H), 7.73-7.76 (m, 1H), 8.44-8.45 (m, 1H), 8.56 (d, J=2.8 Hz, 1H); ESIMS found C10H9FN4 m/z 205 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618128B1
Source datasetuspto-grants-2013_12
ORD IDord-8eba511313e5415e90f57fd82ab34ac4
Source noteuspto-grants-2013_12