Methanol → 3-(Aminomethyl)-4,6-dimethyl-1,2-dihydropyridin-2-one
Reaction equation
[C:1]([C:3]1[C:4](C)([OH:10])[NH:5][CH:6]=[CH:7][C:8]=1[CH3:9])#[N:2].[CH3:12]O>[Ni].N>[NH2:2][CH2:1][C:3]1[C:4](=[O:10])[NH:5][C:6]([CH3:12])=[CH:7][C:8]=1[CH3:9]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
3-Cyano-2,4-dimethyl-2-hydroxypyridine (0.3 g, 2.0 mmol) was dissolved in MeOH (5 mL), to which catalytic amount of Raney Ni and of aqueous NH3 (0.3 mL) were added and the reaction mixture was stirred under hydrogen pressure (bladder pressure) for 3-4 h. After completion of the reaction, catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue was thoroughly dried to provide the desired product (0.3 g, quantitative yield).
Workup
- additionwere added
- customAfter completion of the reaction, catalyst
- filtrationwas filtered off
- concentrationthe filtrate was concentrated under reduced pressure
- customThe residue was thoroughly dried
Sources & evidence
- ORD record
- ord-585d1110f3b142f7912818946a6f346d
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598167B1
Reaction notes
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