Hydrazine → 3-Bromo-4-(4-chlorophenyl)-2-hydrazinyl-6-methylpyridine

HRID 2101377Notes

Reaction equation

HRID 2101377 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]=1

Participants

4

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

  1. stirringthe reaction mixture was stirred at 65° C. for 4 h more
  2. temperatureAfter cooling to room temperature
  3. concentrationthe reaction mixture was concentrated under reduced pressure
  4. additionTo the residue was added water
  5. customthe resulting suspension was sonicated for 5 min
  6. filtrationThe resulting slurry was filtered
  7. washthe collected solid was washed with water (10 mL×2)
  8. 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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