Hydrazine hydrate (1:1) → 1-(6-Hydrazinopyridin-3-yl)-N-methylmethanamine
Reaction equation
Cl[C:2]1[N:7]=[CH:6][C:5]([CH2:8][NH:9][CH3:10])=[CH:4][CH:3]=1.O.[NH2:12][NH2:13]>>[NH:12]([C:2]1[N:7]=[CH:6][C:5]([CH2:8][NH:9][CH3:10])=[CH:4][CH:3]=1)[NH2:13]Participants
3
Procedure
1.0 g (6.4 mmol) of 1-(6-chloropyridin-3-yl)-N-methylmethanamine [for the preparation, see EP 0 556 684-A1] are initially charged in 1.5 ml (1.6 g, 31.9 mmol) of hydrazine hydrate and stirred at boiling point at a bath temperature of 150° C. for 12 h. The reaction solution is cooled and concentrated, and the residue is dried under reduced pressure. This gives 1.1 g of the title compound, which is used without any further purification.
Workup
- customtemperature of 150° C.
- customfor 12 h
- temperatureThe reaction solution is cooled
- concentrationconcentrated
- customthe residue is dried under reduced pressure
- customThis gives 1.1 g of the title compound, which is used without any further purification
Sources & evidence
- ORD record
- ord-86481ec87c4245cea16406c55c7329bf
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08609698B2
Reaction notes
Loading…