Hydrazine → 5-Chloropyridine-3-carbohydrazide
Reaction equation
[NH2:1][NH2:2].[Cl:3][C:4]1[CH:5]=[N:6][CH:7]=[C:8]([CH:13]=1)[C:9](OC)=[O:10]>CO>[Cl:3][C:4]1[CH:5]=[N:6][CH:7]=[C:8]([CH:13]=1)[C:9]([NH:1][NH2:2])=[O:10]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
Hydrazine (17.93 mg, 0.560 mmol) was added to methyl 5-chloronicotinate (80 mg, 0.466 mmol) in methanol (8 mL) and heated overnight at 70° C. The reaction was monitored by TLC. After completion of the reaction, the solvent was removed by vacuum and the compound was purified by column chromatography affording the title compound (40 mg). 1H NMR (400 MHz, CD3OD): δ 8.85 (d, 1H, J=2.0 Hz), 8.70 (d, 1H, J=2.4 Hz), 8.22 (t, 1H, J=2.0 Hz). ESI-MS: 172.0 [M+H]+.
Workup
- customAfter completion of the reaction
- customthe solvent was removed by vacuum
- customthe compound was purified by column chromatography
Sources & evidence
- ORD record
- ord-77b4f9dcdb2148d998f6913a36d6b819
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08987335B2
Reaction notes
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