4-(Pyrimidin-2-yloxy)benzaldehyde → 3-[4-(2-Pyrimidinyloxy)phenyl]-2-propenal
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[O:7][C:8]1[CH:15]=[CH:14][C:11]([CH:12]=O)=[CH:10][CH:9]=1.N1(C2C=C[C:24]([CH:25]=[O:26])=CC=2)C=CC=N1>>[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[O:7][C:8]1[CH:15]=[CH:14][C:11]([CH:12]=[CH:24][CH:25]=[O:26])=[CH:10][CH:9]=1Participants
3
Procedure
The title compound was prepared by a procedure analogous to Reference Example 30 by substituting 4-(2-pyrimidinyloxy)benzaldehyde (prepared as described in Reference Example 9) for the 4-(1H-pyrazol-1-yl)-benzaldehyde of Reference Example 30. MS 227 (M+H)+.
Sources & evidence
- ORD record
- ord-480cdc5e2bda4f4c841c3845029bea18
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472372B1
Reaction notes
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