4-(1H-Pyrazol-1-yl)benzaldehyde → HCID 22631050, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[S:11][CH:10]=[C:9]([CH:12]=O)[CH:8]=1.N1(C2C=C[C:22]([CH:23]=[O:24])=CC=2)C=CC=N1>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[S:11][CH:10]=[C:9](/[CH:12]=[CH:22]/[CH:23]=[O:24])[CH:8]=1Participants
3
Procedure
The title compound is prepared by a procedure analogous to Reference Example 30 by substituting 5-(2-pyridinyl)-3-thiophenecarboxaldehyde (prepared as described in Reference Example 94) or the 4-(1H-pyrazol-1-yl)-benzaldehyde of Reference Example 30. MS 216 (M+H)+.
Sources & evidence
- ORD record
- ord-c4e90a4c0a954f4ab9d0a82d9d5ee2e2
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825170B2
Reaction notes
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