Malonic Acid → 3-[4-(2,6-Dioxo-1,3-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]oct-1-yl]-acrylic acid
Reaction equation
O[CH:2]1[CH:9]2[CH2:10][C:5]3([C:11]4[NH:19][C:18]5[C:17](=[O:20])[N:16]([CH2:21][CH2:22][CH3:23])[C:15](=[O:24])[N:14]([CH2:25][CH2:26][CH3:27])[C:13]=5[N:12]=4)[CH2:6][CH:7](O2)[CH:3]1O3.[C:28]([OH:34])(=[O:33])[CH2:29][C:30](O)=O.N1C=CC=C[CH:36]=1>N1CCCCC1>[O:24]=[C:15]1[N:14]([CH2:25][CH2:26][CH3:27])[C:13]2[N:12]=[C:11]([C:5]34[CH2:7][CH2:3][C:2]([CH:30]=[CH:29][C:28]([OH:34])=[O:33])([CH2:36][CH2:6]3)[CH2:9][CH2:10]4)[NH:19][C:18]=2[C:17](=[O:20])[N:16]1[CH2:21][CH2:22][CH3:23]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
4-(2,6-Dioxo-1,35-dipropyl-2,3,6,7-tetrahydro-1H-purin-8-yl)-bicyclo[2.2.2]octane 1-carbaldehyde (XI, Example 9, 0.490 g, 1.32 mmol) is added to a mixture of malonic acid (0.275 g, 2.64 mmol), pyridine (2 ml), and piperidine (1 drop). The mixture is heated to 1000 for 16 hours. Four additional equivalents of malonic acid are added and heating continued for another 16 hours until consumption of aldehyde ceases, to give the title compound.
Workup
- temperatureThe mixture is heated to 1000 for 16 hours
- temperatureheating
- customcontinued for another 16 hours until consumption of aldehyde ceases
Sources & evidence
- ORD record
- ord-8f61e7dbee1345d9ad728ff8b28bfb6a
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07579354B2
Reaction notes
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