HCID 178432155, compound → 5-Fluoro-2-methylquinazoline
Reaction equation
[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH2:4][NH:5][C:6]([CH3:12])=[N:7]2>C(Cl)(Cl)Cl.[O-2].[Mn+4].[O-2]>[F:1][C:2]1[CH:11]=[CH:10][CH:9]=[C:8]2[C:3]=1[CH:4]=[N:5][C:6]([CH3:12])=[N:7]2Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of 5-fluoro-2-methyl-3,4-dihydroquinazoline (0.74 g, 4.51 mmol) in chloroform (100 mL) at room temperature was added manganese (IV) oxide (4.0 g, 46.0 mmol) and the reaction mixture stirred at room temperature for 20 h. The reaction mixture was filtered through a plug of celite, washing with dichloromethane. The filtrate was evaporated in vacuo to give the title compound as a yellow solid (0.715 g, 98%).
Workup
- filtrationThe reaction mixture was filtered through a plug of celite
- washwashing with dichloromethane
- customThe filtrate was evaporated in vacuo
Sources & evidence
- ORD record
- ord-6eaa548465a9415b9237ea6d78ede64e
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07244726B2
Reaction notes
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