1-Naphthaldehyde → HCID 178469128, compound
Reaction equation
[C:1]1([CH:11]=O)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[NH2:13][C:14]1[CH:18]=[CH:17][NH:16][N:15]=1.[F:19][C:20]([F:30])([F:29])[C:21](=O)[CH2:22][C:23]([O:25][CH2:26][CH3:27])=[O:24]>>[C:1]1([CH:11]2[C:22]([C:23]([O:25][CH2:26][CH3:27])=[O:24])=[C:21]([C:20]([F:19])([F:29])[F:30])[NH:13][C:14]3=[N:15][NH:16][CH:17]=[C:18]23)[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1Participants
4
Procedure
The title compound was prepared from naphthalene-1-aldehyde, 3-aminopyrazole and ethyl trifluoroacetoacetate in the same manner as in Example 1.
Sources & evidence
- ORD record
- ord-b694c15a33b74a2da67ef8826b56fadf
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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