Hydrazine → 3-Bromo-2-hydrazinopyridine

HRID 2189443Notes

Reaction equation

HRID 2189443 reaction equation
[Br:1][C:2]1[C:3](Cl)=[N:4][CH:5]=[CH:6][CH:7]=1.[NH2:9][NH2:10]>N1C=CC=CC=1>[Br:1][C:2]1[C:3]([NH:9][NH2:10])=[N:4][CH:5]=[CH:6][CH:7]=1

Participants

4

Conditions

Temperature
60 °C

Procedure

To a stirring solution of 3-bromo-2-chloropyridine (8.56 g, 45 mmol) in pyridine (40 mL) was added anhydrous hydrazine (4.0 g, 125 mmol). The resulting mixture was stirred at 60° C. for 24 h. Analysis by HPLC indicated that about 50% of starting material was consumed. Additional hydrazine (4.0 g, 125 mmol) was added and the reaction mixture was stirred at 80° C. for another 16 h (total 40 h). After cooling to room temperature, the resulting white suspension was filtered. The collected solid was washed with water (2×50 mL), and dried in a 50° C. vacuum oven for 16 h to afford 5.13 g (61%) of the title compound as a white solid. HPLC/MS (Method C): retention time=0.38 min, [M+H]+=188.0.

Workup

  1. customwas consumed
  2. stirringthe reaction mixture was stirred at 80° C. for another 16 h (total 40 h)
  3. temperatureAfter cooling to room temperature
  4. filtrationthe resulting white suspension was filtered
  5. washThe collected solid was washed with water (2×50 mL)
  6. customdried in a 50° C. vacuum oven for 16 h

Sources & evidence

ORD record
ord-9274df7f5a914b3c9d170b13fdd5c617
Source dataset
uspto-grants-2012_12
Patent number
US08324241B2

Reaction notes

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