Benzaldehyde → HCID 178469129, compound
Reaction equation
[CH:1](=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:9][C:10]1[CH:14]=[CH:13][NH:12][N:11]=1.[F:15][C:16]([F:26])([F:25])[C:17](=O)[CH2:18][C:19]([O:21][CH2:22][CH3:23])=[O:20]>>[C:2]1([CH:1]2[C:18]([C:19]([O:21][CH2:22][CH3:23])=[O:20])=[C:17]([C:16]([F:15])([F:25])[F:26])[NH:9][C:10]3=[N:11][NH:12][CH:13]=[C:14]23)[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Procedure
The title compound was prepared from benzaldehyde, 3-aminopyrazole and ethyl trifluoroacetoacetate in the same manner as in Example 1.
Sources & evidence
- ORD record
- ord-50e102b4dcb3486f966fcdcd31f06c4e
- Source dataset
- uspto-grants-2005_12
- Patent number
- US06977262B2
Reaction notes
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