Hydrazine → 3-Bromo-4-(4-chlorophenyl)-2-hydrazinyl-6-methylpyridine
Reaction equation
[Br:1][C:2]1[C:3](Cl)=[N:4][C:5]([CH3:15])=[CH:6][C:7]=1[C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1.[NH2:17][NH2:18]>O1CCOCC1>[Br:1][C:2]1[C:3]([NH:17][NH2:18])=[N:4][C:5]([CH3:15])=[CH:6][C:7]=1[C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 65 °C
Procedure
To a suspension of 3-bromo-2-chloro-4-(4-chlorophenyl)-6-methylpyridine (0.18 g, 0.56 mmol) in dioxane (4 mL) at room temperature was added anhydrous hydrazine (0.4 mL). The resulting mixture was stirred at 65° C. for 1 h. Analysis by HPLC/MS indicated the reaction was not complete. Additional anhydrous hydrazine (0.3 mL) was added, and the reaction mixture was stirred at 65° C. for 4 h more. After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. To the residue was added water, and the resulting suspension was sonicated for 5 min. The resulting slurry was filtered, and the collected solid was washed with water (10 mL×2), then dried in a 45° C. vacuum oven for 16 h to afford 160 mg (90%) of the title compound as a white solid. HPLC/MS: retention time=2.53 min, [M+H]+=312.1.
Workup
- stirringthe reaction mixture was stirred at 65° C. for 4 h more
- temperatureAfter cooling to room temperature
- concentrationthe reaction mixture was concentrated under reduced pressure
- additionTo the residue was added water
- customthe resulting suspension was sonicated for 5 min
- filtrationThe resulting slurry was filtered
- washthe collected solid was washed with water (10 mL×2)
- customdried in a 45° C. vacuum oven for 16 h
Sources & evidence
- ORD record
- ord-23b1b99cebaa499884ffe966d0dd30d9
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07572808B2
Reaction notes
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