Reaction equation
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][N:3]=1.[OH2:8].C[OH:10].C(Cl)(Cl)Cl>N1C=CC=CC=1.C(Cl)Cl>[N:5]1[CH:6]=[CH:7][C:2]([C:1]([OH:10])=[O:8])=[N:3][CH:4]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 60 °C
Procedure
To a solution of 4-methylpyrimidine (4 g, 46.5 mmol) in pyridine (20 mL) was added SeO2 (8.7 g, 79.06 mmol) at room temperature. The reaction mixture was then heated to 60° C. for 2 h, and then stirred at room temperature for 16 h. The reaction mixture was diluted with DCM (50 mL) and filtered to remove selenium waste. The filtrate was concentrated to give a residue that was stirred with H2O (20 mL), the precipitated solid was filtered and washed with acetone (2×20 mL) and dried to provide (BB12) (3.1 g, 58%) as a brown solid. Rf: 0.2 (40% MeOH/CHCl3). 1H NMR (400 MHz, DMSO-d6): δ 13.8 (1H, br s), 9.37 (1H, s), 9.07 (1H, d, J=5.2 Hz), 8.01 (1H, d, J=4 Hz); m/z 123 (M−H)−.
Workup
- filtrationfiltered
- customto remove selenium waste
- concentrationThe filtrate was concentrated
- customto give a residue that
- filtrationthe precipitated solid was filtered
- washwashed with acetone (2×20 mL)
- customdried
- customto provide (BB12) (3.1 g, 58%) as a brown solid
Sources & evidence
- ORD record
- ord-d035fcd97bf94e418daadc8bb68dc8cf
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08541363B2
Linked notes
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