Methanol → Methyl 2-hydroxy-5-nitronicotinate
Reaction equation
[OH:1][C:2]1[N:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].S(Cl)(Cl)=O.[CH3:18]O>>[N+:11]([C:8]1[CH:7]=[C:3]([C:4]([O:6][CH3:18])=[O:5])[C:2](=[O:1])[NH:10][CH:9]=1)([O-:13])=[O:12]Participants
4
Conditions
- Temperature
- 0 °C
Procedure
To a solution of 2-hydroxy-5-nitronicotinic acid (0.80 g, 4.35 mmol, Combi-Blocks) in methanol (10 mL) at 0° C. was added thionyl chloride (1 mL) dropwise. The mixture was stirred at 0° C. for 1 h, then at 60° C. for 2 h. The excess methanol was removed under reduced pressure and the residue was neutralized with aqueous sodium bicarbonate solution. The solid was collected, washed with water and dried to afford the title compound (0.85 g, 99%). 1H NMR (DMSO-d6) δ 8.44 (s, 1H), 8.34 (s, 1H), 3.67 (s, 3H); MS(ESI+) m/z 199 (M+H)+.
Workup
- waitat 60° C. for 2 h
- customThe excess methanol was removed under reduced pressure
- customThe solid was collected
- washwashed with water
- customdried
Sources & evidence
- ORD record
- ord-25f8f7c4238a4d0b922ed4d2f959a8a1
- Source dataset
- uspto-grants-2008_10
- Patent number
- US07439246B2
Reaction notes
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