2-Methylbenzaldehyde → HCID 136102542, compound
Reaction equation
[N:1]1([C:7]2[N:12]=[CH:11][NH:10][C:9](=[O:13])[CH:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[C:14]1([CH3:22])[C:15]([CH:20]=O)=[CH:16][CH:17]=[CH:18][CH:19]=1>>[CH3:22][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=1[CH2:20][N:4]1[CH2:5][CH2:6][N:1]([C:7]2[N:12]=[CH:11][NH:10][C:9](=[O:13])[CH:8]=2)[CH2:2][CH2:3]1Participants
3
Procedure
6-[4-(2-Methyl-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one was prepared using Procedure A from 6-piperazin-1-yl-3H-pyrimidin-4-one (Intermediate 4) and o-tolualdehyde. Mass spectrum (ES) MH+=285.
Sources & evidence
- ORD record
- ord-2eadd7a8e6ee44cfb8ef7f87ecaa1a02
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07652013B2
Reaction notes
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