Water → HCID 20213009, compound
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6]([NH:8][NH2:9])[CH:5]=[C:4]([C:10]#[N:11])[CH:3]=1.[C:12](Cl)(=[O:14])[CH3:13].O>N1C=CC=CC=1>[C:12]([NH:9][NH:8][C:6]1[CH:5]=[C:4]([C:10]#[N:11])[CH:3]=[C:2]([Cl:1])[N:7]=1)(=[O:14])[CH3:13]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
A suspension of 5.0 g of 6-chloro-2-hydrazinopyridine-4-carbonitrile in 50 ml of pyridine was cooled to 0° C. in an ice bath and 3.1 g of acetyl chloride was added dropwise over a 10 minute period. The mixture became homogeneous after the addition and it was allowed to warm to ambient temperature. After 2 hours, the reaction mixture was poured into 180 ml of water and the precipitate which formed was separated by filtration and dried to give N-acetyl-N'-(6-chloro-4-cyano-2-pyridyl)hydrazine which was purified by recrystallization from ethanol.
Workup
- additionafter the addition and it
- temperatureto warm to ambient temperature
- customthe precipitate which formed
- customwas separated by filtration
- customdried
Sources & evidence
- ORD record
- ord-da48261b9fe440c0b6af20f085874e05
- Source dataset
- uspto-grants-1987_03
- Patent number
- US04650872
Reaction notes
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