3-Bromo-1-phenylpropane-1,2-dione → [6-Ethyl-5-methyl-7-(methylthio)imidazo[1,2-a]pyrimidin-2-yl]phenylmethanone
Reaction equation
[CH2:1]([C:3]1[C:4]([CH3:12])=[N:5][C:6]([NH2:11])=[N:7][C:8]=1[S:9][CH3:10])[CH3:2].Br[CH2:14][C:15](=O)[C:16]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)=[O:17]>CCOCC>[CH2:1]([C:3]1[C:8]([S:9][CH3:10])=[N:7][C:6]2[N:5]([CH:14]=[C:15]([C:16]([C:18]3[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=3)=[O:17])[N:11]=2)[C:4]=1[CH3:12])[CH3:2]Participants
Procedure
A stirred suspension of 4.5 g of 5-ethyl-4-methyl -6-methylthio-2-pyrimidinamine in 28 ml of ether was treated with 5.5 g of 3-bromo-1-phenylpropane-1,2-dione to obtain a yellow solution. After standing two days at room temperature, the crystallized pyrimidinium salt was filtered off, washed with ether and heated for one hour in refluxing ethanol. The solution was evaporated to dryness under reduced pressure and the residue was shaken with a mixture of chloroform and aqueous potassium carbonate. The organic layer was washed, dried over MgSO4 and evaporated to dryness under reduced pressure. Trituration of the residue with ethanol and filtration yielded 4.1 g (53% yield) of [6-ethyl-5-methyl-7-(methylthio)imidazo[1,2-a]pyrimidin-2-yl]phenylmethanone after recrystallization from methanol in the form of a buff solid.
Workup
- customto obtain a yellow solution
- filtrationthe crystallized pyrimidinium salt was filtered off
- washwashed with ether
- temperatureheated for one hour
- temperaturein refluxing ethanol
- customThe solution was evaporated to dryness under reduced pressure
- washThe organic layer was washed
- dry with materialdried over MgSO4
- customevaporated to dryness under reduced pressure
- filtrationTrituration of the residue with ethanol and filtration
Sources & evidence
- ORD record
- ord-a837c33804f048dd8dd77c5ecabe3cd0
- Source dataset
- uspto-grants-1985_07
- Patent number
- US04532243
Reaction notes
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