4-Methylpyrimidine-2-carbonitrile → 4-Methyl-2-pyrimidinemethanamine
Reaction equation
[C:1]([C:3]1[N:8]=[C:7]([CH3:9])[CH:6]=[CH:5][N:4]=1)#[N:2].[H][H]>CO.[Pd]>[CH3:9][C:7]1[CH:6]=[CH:5][N:4]=[C:3]([CH2:1][NH2:2])[N:8]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a nitrogen flushed solution of the title compound from Step A (1 g, 8.39 mmol) in methanol (40 ml) was added 10% palladium on carbon (100 mg) and the resulting mixture stirred under a balloon of hydrogen for 3 h. The mixture was filtered through celite and evaporated to give 950 mg (91%) of the title compound (i-6) as an orange oil. 1H NMR (CDCl3): 2.54 (s, 3H), 4.16 (s, 2H), 7.03 (d, J 5.0 Hz, 1H), 8.56 (d, J 5.0 Hz, 1H).
Workup
- filtrationThe mixture was filtered through celite
- customevaporated
Sources & evidence
- ORD record
- ord-d82d114b8f104d9080f19b05be1d3d5d
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08354403B2
Reaction notes
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