Benzene, 1-bromo-3,5-dimethyl- → 6-(2-Aminoethyl)-5-(3,5-dimethylphenyl)-1,3-dimethyl-1H-pyrrolo[3,4-d]pyrimidine-2,4(3H,6H)-dione
Reaction equation
[NH2:1][CH2:2][CH2:3][N:4]1[C:12](C2C=CC=C(Cl)C=2)=[C:11]2[C:6]([N:7]([CH3:23])[C:8](=[O:22])[N:9]([CH3:21])[C:10]2=[O:20])=[CH:5]1.Br[C:25]1[CH:30]=[C:29]([CH3:31])[CH:28]=[C:27]([CH3:32])[CH:26]=1>>[NH2:1][CH2:2][CH2:3][N:4]1[C:12]([C:25]2[CH:30]=[C:29]([CH3:31])[CH:28]=[C:27]([CH3:32])[CH:26]=2)=[C:11]2[C:6]([N:7]([CH3:23])[C:8](=[O:22])[N:9]([CH3:21])[C:10]2=[O:20])=[CH:5]1Participants
3
Procedure
The title compound was prepared analogously to Intermediate B by replacing 1-bromo-3-chlorobenzene with 1-bromo-3,5-dimethylbenzene;
Sources & evidence
- ORD record
- ord-5a227009cea84688a69d34ade3af5fa5
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09303035B2
Reaction notes
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