Carbonate Ion → 3,7-Diethyl-1-(6-hydroxy-6-methylheptyl)-xanthine
Reaction equation
[CH2:1]([N:3]1[C:11]2[N:10]=[CH:9][N:8]([CH2:12][CH3:13])[C:7]=2[C:6](=[O:14])[NH:5][C:4]1=[O:15])[CH3:2].C(=O)([O-])[O-].Br[CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][C:26]([OH:29])([CH3:28])[CH3:27]>CN(C)C=O>[CH2:1]([N:3]1[C:11]2[N:10]=[CH:9][N:8]([CH2:12][CH3:13])[C:7]=2[C:6](=[O:14])[N:5]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][C:26]([OH:29])([CH3:28])[CH3:27])[C:4]1=[O:15])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
6.2 g of 3,7-diethylxanthine, 4.1 g of ptassium carbonate, and 6.6 g of 1-bromo-6-hydroxy-6-methylheptane are stirred in 100 ml of dimethylformamide at 120° C. for 18 hours. The mixture is filtered hot with suction, the filtrate is concentrated under recuced pressure final recrystallization from diisopropylether with addition of petroleum ether.
Workup
- filtrationThe mixture is filtered hot with suction
- concentrationthe filtrate is concentrated under recuced pressure final
- customrecrystallization from diisopropylether
- additionwith addition of petroleum ether
Sources & evidence
- ORD record
- ord-99b567231b784caa8db1791373953f7c
- Source dataset
- uspto-grants-1992_04
- Patent number
- US05109003
Reaction notes
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