4-Quinolinecarboxaldehyde → 3-(Quinolin-4-yl)prop-2-enal
Reaction equation
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([CH:11]=O)=[CH:3][CH:2]=1.N1(C2C=C[C:21]([CH:22]=[O:23])=CC=2)C=CC=N1>>[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]([CH:11]=[CH:21][CH:22]=[O:23])=[CH:3][CH:2]=1Participants
3
Procedure
The title compound was prepared by a procedure analogous to Reference Example 30 by substituting 4-quinolinecarboxaldehyde for the 4-(1H-pyrazol-1-yl)-benzaldehyde of Reference Example 30. MS 184 (M+H)+.
Sources & evidence
- ORD record
- ord-896b7ca29ac84e21acd564b721d74fb1
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06613747B2
Reaction notes
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