HuagongsheHuagongshe Chemistry Print Report · For research reference only
5'-Fluoro-5-nitro-3,3'-bipyridin-4-amine → 5'-Fluoro-3,3'-bipyridine-4,5-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5'-Fluoro-5-nitro-3,3'-bipyridin-4-amine | HCID 86701065 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5'-Fluoro-3,3'-bipyridine-4,5-diamine | HCID 86701066 | 100% |
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→3:97 MeOH[7N NH3]:CHCl3) to produce 5′-fluoro-3,3′-bipyridine-4,5-diamine (LXXII) 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883822B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-09c82c58e3e54b108df5c9249444259e |
| Source note | uspto-grants-2014_11 |