Methylamine → n-Methyl-3-nitropyridin-4-amine
Reaction equation
Cl[C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9].[CH3:11][NH2:12]>C(O)C>[CH3:11][NH:12][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][C:3]=1[N+:8]([O-:10])=[O:9]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
29.9 g of (9) were solubilised in 200 ml of hot ethanol; to the solution, brought to 0° C., were added slowly, dropwise, 103 ml of 35% aqueous methylamine. This was left stirring for 30 minutes and then the ethanol evaporated. The residue was crystallised in water giving 24 g of (10) in the form of clear yellow crystals.
Workup
- custombrought to 0° C.
- additionwere added slowly
- waitThis was left
- customthe ethanol evaporated
- customThe residue was crystallised in water giving 24 g of (10) in the form of clear yellow crystals
Sources & evidence
- ORD record
- ord-76ecf2d1884147a08237cf81eb10517c
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07230102B2
Reaction notes
Loading…