4-(5-nitropyridin-2-yl)benzaldehyde → HCID 22630900, compound
Reaction equation
[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10]2[CH:17]=[CH:16][C:13]([CH:14]=O)=[CH:12][CH:11]=2)=[N:8][CH:9]=1)([O-:3])=[O:2].N1(C2C=C[C:26]([CH:27]=[O:28])=CC=2)C=CC=N1>>[N+:1]([C:4]1[CH:5]=[CH:6][C:7]([C:10]2[CH:17]=[CH:16][C:13](/[CH:14]=[CH:26]/[CH:27]=[O:28])=[CH:12][CH:11]=2)=[N:8][CH:9]=1)([O-:3])=[O:2]Participants
3
Procedure
The title compound was prepared by a procedure analogous to Reference Example 30 by substituting 4-(5-nitro-2-pyridinyl)benzaldehyde (prepared as described in Reference Example 19) for the 4-(1H-pyrazol-1-yl)-benzaldehyde of Reference Example 30. MS 255 (M+H)+.
Sources & evidence
- ORD record
- ord-b7756946e02b4a168986e3509f68cc12
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06825170B2
Reaction notes
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