2-Methoxy-1-naphthaldehyde → HCID 178439519, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]=1[CH:13]=O.[NH2:15][C:16]1[CH:20]=[CH:19][NH:18][N:17]=1.O=[C:22]([CH2:29][CH2:30][CH3:31])[CH2:23][C:24]([O:26][CH2:27][CH3:28])=[O:25]>>[CH3:1][O:2][C:3]1[CH:12]=[CH:11][C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[C:4]=1[CH:13]1[C:23]([C:24]([O:26][CH2:27][CH3:28])=[O:25])=[C:22]([CH2:29][CH2:30][CH3:31])[NH:15][C:16]2=[N:17][NH:18][CH:19]=[C:20]12Participants
4
Procedure
The title compound was prepared from 2-methoxynaphthalene-1-aldehyde, 3-aminopyrazole and ethyl 3-ketohexanoate in the same manner as in Example 25.
Sources & evidence
- ORD record
- ord-f8fa0736e51247d9858f734fd4f23b82
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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