Ethanol → 3-Amino-5-chloropyridine-2-carboxamide
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N+:10]([O-])=O)[C:5]([C:8]#[N:9])=[N:6][CH:7]=1.CC[OH:15]>>[NH2:10][C:4]1[C:5]([C:8]([NH2:9])=[O:15])=[N:6][CH:7]=[C:2]([Cl:1])[CH:3]=1Participants
3
Procedure
Raney Nickel (10 g of Aldrich 50% slurry in water) was washed with water (100 mL), 5% AcOH (100 mL), water (100 mL), and 95% EtOH (3×100 mL). The resulting slurry was added to a solution of 5-chloro-3-nitropicolinonitrile (104) (5.0 g, 27 mmol) in 95% EtOH (100 mL). The mixture was hydrogenated at 45 psi for 2.5 h. The mixture was then filtered over a bed of Celite and washed with 95% EtOH (2×100 mL). The red/brown filtrate was rota-evaporated to dryness, leaving the title compound as a light brown solid, 3.8 g (82%), mp 152°-6° C. (Lit., 165°-6° C., McCaustland and Cheng, J. Heterocycl. Chem. 7:467 (1970)); 1H NMR (CDCl3): δ5.42 (bs, 1H), 6.05 (bs, 2H), 7.00 (d, J=1.2 Hz, 1H), 7.71 (bs, 1H), 7.79 (d, J=1.2 Hz, 1H).
Workup
- washRaney Nickel (10 g of Aldrich 50% slurry in water) was washed with water (100 mL), 5% AcOH (100 mL), water (100 mL), and 95% EtOH (3×100 mL)
- filtrationThe mixture was then filtered over a bed of Celite
- washwashed with 95% EtOH (2×100 mL)
- customThe red/brown filtrate was rota-evaporated to dryness
Sources & evidence
- ORD record
- ord-fe0fa1e2735a47e28e7dd66a715ea9ff
- Source dataset
- uspto-grants-1998_09
- Patent number
- US05801183
Reaction notes
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